55 results
Search Results
2. Combined SERS-Raman screening of HER2-overexpressing or silenced breast cancer cell lines.
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Spaziani, Sara, Esposito, Alessandro, Barisciano, Giovannina, Quero, Giuseppe, Elumalai, Satheeshkumar, Leo, Manuela, Colantuoni, Vittorio, Mangini, Maria, Pisco, Marco, Sabatino, Lina, De Luca, Anna Chiara, and Cusano, Andrea
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BREAST ,RNA interference ,BREAST cancer ,EPIDERMAL growth factor receptors ,CANCER cells ,CELL lines ,MAMMOGRAMS - Abstract
Background: Breast cancer (BC) is a heterogeneous neoplasm characterized by several subtypes. One of the most aggressive with high metastasis rates presents overexpression of the human epidermal growth factor receptor 2 (HER2). A quantitative evaluation of HER2 levels is essential for a correct diagnosis, selection of the most appropriate therapeutic strategy and monitoring the response to therapy. Results: In this paper, we propose the synergistic use of SERS and Raman technologies for the identification of HER2 expressing cells and its accurate assessment. To this end, we selected SKBR3 and MDA-MB-468 breast cancer cell lines, which have the highest and lowest HER2 expression, respectively, and MCF10A, a non-tumorigenic cell line from normal breast epithelium for comparison. The combined approach provides a quantitative estimate of HER2 expression and visualization of its distribution on the membrane at single cell level, clearly identifying cancer cells. Moreover, it provides a more comprehensive picture of the investigated cells disclosing a metabolic signature represented by an elevated content of proteins and aromatic amino acids. We further support these data by silencing the HER2 gene in SKBR3 cells, using the RNA interference technology, generating stable clones further analysed with the same combined methodology. Significant changes in HER2 expression are detected at single cell level before and after HER2 silencing and the HER2 status correlates with variations of fatty acids and downstream signalling molecule contents in the context of the general metabolic rewiring occurring in cancer cells. Specifically, HER2 silencing does reduce the growth ability but not the lipid metabolism that, instead, increases, suggesting that higher fatty acids biosynthesis and metabolism can occur independently of the proliferating potential tied to HER2 overexpression. Conclusions: Our results clearly demonstrate the efficacy of the combined SERS and Raman approach to definitely pose a correct diagnosis, further supported by the data obtained by the HER2 gene silencing. Furthermore, they pave the way to a new approach to monitor the efficacy of pharmacologic treatments with the aim to tailor personalized therapies and optimize patients' outcome. [ABSTRACT FROM AUTHOR]
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- 2024
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3. Navigating challenges: optimising methods for primary cell culture isolation.
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Piwocka, Oliwia, Musielak, Marika, Ampuła, Karolina, Piotrowski, Igor, Adamczyk, Beata, Fundowicz, Magdalena, Suchorska, Wiktoria Maria, and Malicki, Julian
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CELL separation ,CELL culture ,CELL populations ,CELL lines ,CANCER cells - Abstract
Primary cell lines are invaluable for exploring cancer biology and investigating novel treatments. Despite their numerous advantages, primary cultures are laborious to obtain and maintain in culture. Hence, established cell lines are still more common. This study aimed to evaluate a range of techniques for isolating primary breast cancer cultures, employing distinct enzymatic compositions, incubation durations, and mechanical approaches, including filtration. Out of several protocols, we opted for a highly effective method (Method 5) that gave rise to a primary cell culture (BC160). This method combines mechanical disaggregation and enzymatic digestion with hyaluronidase and collagenase. Moreover, the paper addresses common issues in isolating primary cultures, shedding light on the struggle against fibroblasts overgrowing cancer cell populations. To make primary cell lines a preferred model, it is essential to elaborate and categorise isolation methods, develop approaches to separate heterogeneous cultures and investigate factors influencing the establishment of primary cell lines. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Network pharmacology, molecular docking, and in vitro study on Aspilia pluriseta against prostate cancer.
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Okpako, Innocent Oluwaseun, Ng'ong'a, Florence Atieno, Kyama, Cleophas Mutinda, and Njeru, Sospeter Ngoci
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COMPUTER-assisted molecular modeling ,IN vitro studies ,MITOGEN-activated protein kinases ,RESEARCH funding ,T-test (Statistics) ,DATA analysis ,PHARMACEUTICAL chemistry ,POLYMERASE chain reaction ,CELL proliferation ,PROSTATE tumors ,PLANT roots ,PHYTOCHEMICALS ,CELLULAR signal transduction ,GAS chromatography ,CELL lines ,GENE expression ,MEDICINAL plants ,MOLECULAR structure ,MASS spectrometry ,ONE-way analysis of variance ,STATISTICS ,CALORIMETRY ,DATA analysis software - Abstract
Background: Current prostate cancer treatments are associated with life-threatening side effects, prompting the search for effective and safer alternatives. Aspilia pluriseta Schweinf. ex Engl. has previously shown anticancer activity in lung and liver cancer cell lines. This study investigated its potential for prostate cancer. Methods: A crude extract of A. pluriseta root was prepared using dichloromethane/methanol (1:1 v/v) and partitioned into hexane, ethyl acetate, and water fractions. The MTT assay was used to assess the antiproliferative activity of the fractions. The active fractions were tested at 6.25–200 µg/ml on human prostate cancer DU-145 cells and non-cancerous Vero E6 cells. Qualitative phytochemical and gas chromatography-mass spectrometry (GC-MS) analyses were conducted to identify chemical compounds. Network pharmacology was employed to predict molecular targets and modes of action of the identified chemical compounds, with subsequent validation through molecular docking and real-time PCR. Results: Active extracts included crude dichloromethane/methanol, hexane, and ethyl acetate fractions, inhibiting DU-145 cell proliferation with IC
50 values of 16.94, 20.06, and 24.14 µg/ml, respectively. Selectivity indices were determined to be 6.04 (crude), 3.62 (hexane), and 6.68 (ethyl acetate). Identified phytochemicals comprised phenols, terpenoids, flavonoids, tannins, sterols, and saponins. GC-MS analysis revealed seventy-nine (79) compounds, with seven (7) meeting ideal drug candidate parameters; their hub gene targets included MAPK3, MAPK1, IL6, TP53, ESR1, PTGS2, MMP9, MDM2, AR, and MAP2K1, implicating regulation of PI3K/Akt, MAPK, and p53 signaling pathways as potential modes of action. Core compounds such as 1-heneicosanol, lanosterol, andrographolide, and retinoic acid exhibited strong binding activities, particularly lanosterol with MAPK21 (-9.7 kcal/mol), ESR1 (-8.9 kcal/mol), and MAPK3 (-8.8 kcal/mol). Treatment with A. pluriseta downregulated AR expression and upregulated p53, while also downregulating CDK1 and BCL-2 and upregulating caspase-3. Conclusions: A. pluriseta extracts inhibited DU-145 cell growth without causing cellular toxicity, suggesting great potential for development as an anti-prostate cancer agent. However, further in vitro and in vivo experiments are recommended. [ABSTRACT FROM AUTHOR]- Published
- 2024
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5. Evaluation of chicken embryo extract and egg yolk extract as alternatives to basic cell culture medium supplement.
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Mulugeta, Fregenet, Degefa, Teferi, Mulugeta, Demise, Alemu, Anberber, Beka, Jitu, Ferede, Henok, Woldemichael, Dereje Nigussie, and Woldemariyam, Fanos Tadesse
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EGG yolk ,HARD currencies ,CELL lines ,CELL survival ,CALVES ,CHICKEN embryos - Abstract
Background: Fetal calf serum (FCS), an existing cell culture supplement, is effective but has several drawbacks, including being expensive, requiring a lengthy process of production, and requiring a hard currency. With this in mind, we planned to evaluate chick embryo extract and egg yolk extracts in cell culture as alternatives to fetal calf serum (FCS). Methods: Specific pathogen-free eggs were purchased from the National Veterinary Institute, Bishoftu, Ethiopia, and incubated in a humidified incubator at 37 °C for 11 days. Egg yolk extract (EYE) and chick embryo extract (CEE) were collected after the egg was opened with caution not to destroy the yolk sack or the chick embryo itself. Chick fibroblasts and Vero cells were cultured in minimum essential medium (MEM) supplemented with egg yolk extract or chick embryo extract at ratios of 0:10, 1:9, 2.5:7.5, and 5:5% fetal calf serum. Results: Fibroblast cell attachment was better in media supplemented with 5% CEE and 5% FCS. The confluency was also greater than 50% at this concentration. Vero cells cultured with 5% CEE and 5% FCS also exhibited very good cell attachment and a confluency of up to 70%. Viability and confluency were also observed at 5%:5% ratios of 50 and 70%, respectively. Conclusion: This investigation evaluated these two extracts as cell culture supplements and revealed promising results as alternatives to fetal calf serum. The limitation of this study is that it only used two cell types and additional cell lines, and different ratios should be tested. With the above findings, further research using different cell lines, ratios and conditions is warranted. [ABSTRACT FROM AUTHOR]
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- 2024
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6. Turkish coffee has an antitumor effect on breast cancer cells in vitro and in vivo.
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Amin, Mohamed N., Abdelmohsen, Usama Ramadan, and Samra, Yara A.
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IN vitro studies ,BIOLOGICAL models ,COFFEE ,TRADITIONAL medicine ,COLORIMETRY ,ANTINEOPLASTIC agents ,BREAST tumors ,APOPTOSIS ,CELL proliferation ,ENZYME-linked immunosorbent assay ,IN vivo studies ,OXIDATIVE stress ,DESCRIPTIVE statistics ,CYTOSKELETAL proteins ,PLANT extracts ,CELL lines ,MICE ,GENE expression ,IMMUNOHISTOCHEMISTRY ,ANIMAL experimentation ,MEMBRANE glycoproteins ,ORGANIC compounds ,PEROXISOME proliferator-activated receptors ,CASPASES ,MALONDIALDEHYDE ,PHARMACODYNAMICS - Abstract
Background: Breast cancer is the most diagnosed cancer in women. Its pathogenesis includes several pathways in cancer proliferation, apoptosis, and metastasis. Some clinical data have indicated the association between coffee consumption and decreased cancer risk. However, little data is available on the effect of coffee on breast cancer cells in vitro and in vivo. Methods: In our study, we assessed the effect of Turkish coffee and Fridamycin-H on different pathways in breast cancer, including apoptosis, proliferation, and oxidative stress. A human breast cancer cell line (MCF-7) was treated for 48 h with either coffee extract (5% or 10 v/v) or Fridamycin-H (10 ng/ml). Ehrlich solid tumors were induced in mice for in vivo modeling of breast cancer. Mice with Ehrlich solid tumors were treated orally with coffee extract in drinking water at a final concentration (v/v) of either 3%, 5%, or 10% daily for 21 days. Protein expression levels of Caspase-8 were determined in both in vitro and in vivo models using ELISA assay. Moreover, P-glycoprotein and peroxisome proliferator-activated receptor gamma (PPAR-γ) protein expression levels were analyzed in the in vitro model. β-catenin protein expression was analyzed in tumor sections using immunohistochemical analysis. In addition, malondialdehyde (MDA) serum levels were analyzed using colorimetry. Results: Both coffee extract and Fridamycin-H significantly increased Caspase-8, P-glycoprotein, and PPAR-γ protein levels in MCF-7 cells. Consistently, all doses of in vivo coffee treatment induced a significant increase in Caspase-8 and necrotic zones and a significant decrease in β- catenin, MDA, tumor volume, tumor weight, and viable tumor cell density. Conclusion: These findings suggest that coffee extract and Fridamycin-H warrant further exploration as potential therapies for breast cancer. [ABSTRACT FROM AUTHOR]
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- 2024
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7. Phytochemical and biological investigation of Astragalus Caprinus L.
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Abdallah, Walid E., Abdelshafeek, Khaled A., Elsayed, Wael M., AbdelMohsen, Mona M., Salah, Neven A., and Hassanein, Heba D.
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ORGANIC compound analysis ,ASTRAGALUS (Plants) ,GRAM-positive bacterial infections ,FLAVONOIDS ,ANTIMICROBIAL stewardship ,PHYTOCHEMICALS ,PLANT roots ,STAPHYLOCOCCUS aureus ,DESCRIPTIVE statistics ,PLANT extracts ,CELL lines ,GAS chromatography ,CANDIDA albicans ,METABOLITES ,ANTI-infective agents ,MEDICINAL plants ,MASS spectrometry ,BACTERIAL diseases ,ETHERS ,FATTY acids ,GRAM-negative bacterial diseases ,DATA analysis software ,PSEUDOMONAS ,KLEBSIELLA - Abstract
Background: cultivated and wild plants are used to treat different ailments. The Astragalus genus is found in temperate and dry climates; thus, it is found in Egypt and the arab world. Astragalus caprinus has a good amount of bioactive chemicals, which may help explain its therapeutic effects in reducing the risk of consequences from disease. Method: The phytochemical investigation of the herb and roots of Astragalus caprinus L. included the analytical characterization for the petroleum ether components by GC/MS, unsaponifiable matter (unsap. fraction), and fatty acids (FAME) investigation by GLC analysis. Main flavonoids were chromatographically isolated from ethyl acetate and n-butanol extracts. In vitro antimicrobial activity has been tested against the Gram-positive bacteria Staphylococcus aureus and Streptococcus mutans for different plant extracts, the Gram-negative bacteria Pseudomonas aeruginosa and Klebsiella pneumonia, the fungus Candida albicans and Aspergillus niger, and the Escherichia coli bacterium. Metabolite cytotoxicity was examined using the MTT assay against HepG-2 (human liver carcinoma) and MCF-7 (breast carcinoma). Results: Identifying the important components of the herb and root petroleum ether extracts was achieved. Using column chromatography, luteolin, cosmosiin (apigenin-7-O-glucoside), and cynaroside (luteolin-7-O-glucoside) were separated and identified using UV, NMR, and Mass Spectroscopy. Root extracts displayed potential antimicrobial activity against most of the tested pathogens. Both extracts (herb and roots) were active against the MCF-7 cell line and HepG-2 cell line with IC
50 62.5 ± 0.64 and 72.4 ± 2.3 µg/ml, and 75.9 ± 2.5 and 96.8 ± 4.2 µg/ml, respectively. Conclusion: Astragalus caprinus seems to be a promising source of bioactive compounds that could potentially aid in preventing disease complications and address common health issues in developing countries. Moreover, the various parts of this plant could be utilized as natural raw materials for producing health-boosting products that could address common health issues in developing countries. [ABSTRACT FROM AUTHOR]- Published
- 2024
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8. Apoptosis induction and inhibition of invasion and migration in gastric cancer cells by Isoorientin studied using network pharmacology.
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Song, Dan, Chen, Maosheng, Chen, Xiangjun, Xu, Jiaojiao, Wu, Siqi, Lyu, Yaxin, and Zhao, Qin
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THERAPEUTIC use of antineoplastic agents ,FLOW cytometry ,MITOCHONDRIAL membranes ,STOMACH tumors ,CANCER invasiveness ,RESEARCH funding ,ANTINEOPLASTIC agents ,APOPTOSIS ,CELL proliferation ,PHARMACEUTICAL chemistry ,POLYMERASE chain reaction ,CELL motility ,TREATMENT effectiveness ,CELL cycle ,DESCRIPTIVE statistics ,CELLULAR signal transduction ,METASTASIS ,FLAVONES ,CELL lines ,GENE expression ,BIOINFORMATICS ,CELL culture ,RNA ,MOLECULAR structure ,WESTERN immunoblotting ,MTOR inhibitors ,COMPARATIVE studies ,CELL survival ,CASPASES ,PHARMACODYNAMICS - Abstract
Background: To investigate the effects of Isoorientin on the apoptosis, proliferation, invasion, and migration of human gastric cancer cells (HGC27 cells). Methods: We used network pharmacology to predict the targets of drugs and diseases. The CCK-8 assay was used to determine the effects of Isoorientin on the proliferation of HGC27 cells. Flow cytometry was employed to analyze the effects of Isoorientin on cell apoptosis and cell cycle distribution of HGC27 cells. Scratch test and transwell chamber test were conducted to assess the effects of Isoorientin on invasion and migration, respectively. Additionally, qPCR and western blot were performed to examine the impact of Isoorientin on apoptosis-related genes and protein expression, respectively. Results: The Isoorientin significantly inhibited the proliferation, migration, and invasion of HGC27 cells compared to the control group. Furthermore, Isoorientin induced apoptosis in HGC27 cells by upregulating the relative expression of Bax and caspase-3 while downregulating the relative expression of p-PI3K, p-AKT, and Bcl-2 proteins. Conclusion: The Isoorientin exhibits inhibitory effects on the proliferation, invasion, and migration of HGC27 cells, and induces apoptosis in gastric cancer cells. [ABSTRACT FROM AUTHOR]
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- 2024
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9. Insights into free radicals scavenging, α-Amylase inhibition, cytotoxic and antifibrotic activities unveiled by Peganum harmala extracts.
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Jaradat, Nidal, Hawash, Mohammed, Sharifi-Rad, Majid, Shakhshir, Ali, Sobuh, Shorooq, Hussein, Fatima, Issa, Linda, Hamamrhe, Sondos, Al-Sheikh, Eman, and Ibrahim, Alaa Naser
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ANTI-inflammatory agents ,EPITHELIAL cells ,DATA analysis ,ESSENTIAL oils ,HYPOGLYCEMIC agents ,DESCRIPTIVE statistics ,PLANT extracts ,SEEDS ,CYTOTOXINS ,FIBROSIS ,CELL lines ,FREE radical scavengers ,MEDICINAL plants ,ONE-way analysis of variance ,STATISTICS ,FLUOROURACIL ,BIOLOGICAL assay ,DATA analysis software ,AMYLASES ,PHARMACODYNAMICS ,CHEMICAL inhibitors - Abstract
Background: Peganum harmala L. is used in traditional medicine to treat several health ailments. Hence, the present work aimed to investigate the DPPH free radical scavenging, α-amylase, cytotoxic, and antifibrotic effects of the hydrophilic extract and fixed oil obtained from P. harmala seeds. Methods: The hydrophilic extract and fixed oil of P. harmala were assessed for their abilities to scavenge DPPH free radicals and inhibit α-amylase using reference bioassays. The cytotoxicity was assessed on several cancer and normal cell lines, including B16F1, Caco-2, COLO205, HeLa, Hep 3B and Hep G2, MCF-7, and HEK-293 T cells. The MTS assay was used to evaluate the antifibrotic capabilities utilizing the human hepatic stellate (LX-2) cell line. Results: P. harmala plant fixed oil has potent DPPH free radical scavenging activity with an IC
50 dose of 79.43 ± 0.08 µg/ml. Besides, the hydrophilic extract has a poor anti-α-amylase effect compared with the antidiabetic drug Acarbose, with IC50 doses of 398 ± 0.59 and 25.11 ± 1.22 µg/ml, respectively. In addition, the growth of MCF-7, Hep3B, HepG2, HeLa, COLO205, CaCo2, B16F1, and HeK293t was inhibited by P. harmala hydrophilic extract with IC50 doses of 121.34 ± 1.71, 268.3 ± 0.75, 297.20 ± 1.00, 155.60 ± 1.14, 150.01 ± 0.51, 308.35 ± 0.53, 597.93 ± 1.36, and 5.38 ± 0.99 µg/ml, respectively. In addition, at 1000 µg/ml, 5-Fluorouracil reduced fibrosis cells by 0.089%, while the hydrophilic extract decreased the number of LX-2 cells by 5.81%. Conclusion: P. harmala plant-fixed oil exhibits potential antioxidant properties. While the hydrophilic extract showed limited effectiveness as an anti-α-amylase agent and demonstrated notable cytotoxic effects against various tested cancer cell lines. Furthermore, this extract significantly reduces the number of LX-2 fibrotic cells. These findings emphasize the therapeutic potential of these products in managing various health disorders and warrant further investigation into their mechanisms of action and clinical applications. [ABSTRACT FROM AUTHOR]- Published
- 2024
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10. The antioxidant and antimicrobial activity of ethanolic extract in roots, stems, and leaves of three commercial Cymbopogon species.
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Wahyuni, Dwi Kusuma, Kharisma, Viol Dhea, Murtadlo, Ahmad Affan Ali, Rahmawati, Cici Tya, Syukriya, Alvi Jauharotus, Prasongsuk, Sehanat, Subramaniam, Sreeramanan, Wibowo, Anjar Tri, and Purnobasuki, Hery
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THERAPEUTIC use of antioxidants ,IN vitro studies ,COMPUTER-assisted molecular modeling ,RESEARCH funding ,BACILLUS (Bacteria) ,STAPHYLOCOCCAL diseases ,PLANT stems ,DRUG resistance in microorganisms ,PLANT roots ,CELLULAR signal transduction ,DESCRIPTIVE statistics ,PLANT extracts ,ANTI-infective agents ,GAS chromatography ,CELL lines ,METABOLITES ,MASS spectrometry ,ESCHERICHIA coli diseases ,MOLECULAR structure ,LEMONGRASS ,LEAVES ,CANDIDIASIS ,DATA analysis software ,TOXICITY testing - Abstract
Background: Cymbopogon is a member of the family Poaceae and has been explored for its phytochemicals and bioactivities. Although the antimicrobial activities of Cymbopogon spp. extracts have been extensively studied, comprehensive analyses are required to identify promising compounds for the treatment of antimicrobial resistance. Therefore, this study investigated the antioxidant and antimicrobial properties of Cymbopogon spp. ethanolic extracts in every single organ. Methods: Ethanolic extracts were obtained from three Indonesian commercial species of Cymbopogon spp., namely Cymbopogon citratus (L.) Rendle, Cymbopogon nardus (DC.) Spatf., and Cymbopogon winterianus Jowitt. The leaf, stem, and root extracts were evaluated via metabolite profiling using gas chromatography-mass spectrometry (GC–MS). In silico and in vitro analyses were used to evaluate the antioxidant and antimicrobial properties of the Cymbopogon spp. ethanolic extracts. In addition, bioactivity was measured using cytotoxicity assays. Antioxidant assays were performed using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2-azino-bis [3-ethylbenzothiazoline-6-sulfonic acid (ABTS) to determine toxicity to Huh7it-1 cells using a tetrazolium bromide (MTT) assay. Finally, the antimicrobial activity of these extracts was evaluated against Candida albicans, Bacillus subtilis, Staphylococcus aureus, and Escherichia coli using a well diffusion assay. Results: GC–MS analysis revealed 53 metabolites. Of these, 2,5-bis(1,1-dimethylethyl)- phenol (27.87%), alpha-cadinol (26.76%), and 1,2-dimethoxy-4-(1-propenyl)-benzene (20.56%) were the predominant compounds. C. winterianus and C. nardus leaves exhibited the highest antioxidant activity against DPPH and ABTS, respectively. Contrastingly, the MTT assay showed low cytotoxicity. C. nardus leaf extract exhibited the highest antimicrobial activity against E. coli and S. aureus, whereas C. winterianus stem extract showed the highest activity against B. substilis. Furthermore, computational pathway analysis predicted that antimicrobial activity mechanisms were related to antioxidant activity. Conclusions: These findings demonstrate that the leaves had strong antioxidant activity, whereas both the leaves and stems showed great antimicrobial activity. Furthermore, all Cymbopogon spp. ethanolic extracts showed low toxicity. These findings provide a foundation for future studies that assess the clinical safety of Cymbopogon spp. as novel drug candidates. [ABSTRACT FROM AUTHOR]
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- 2024
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11. The efficacy and potential mechanisms of pyrotinib in targeting EGFR and HER2 in advanced oral squamous cell carcinoma.
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Zhou, Liang, Le, Kehao, Chen, Qianming, and Wang, Huiming
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THERAPEUTIC use of antineoplastic agents ,SQUAMOUS cell carcinoma ,TISSUE arrays ,IN vitro studies ,WOUND healing ,PEARSON correlation (Statistics) ,MOUTH tumors ,COLONY-forming units assay ,PHOSPHORYLATION ,T-test (Statistics) ,DATA analysis ,PROTEIN-tyrosine kinase inhibitors ,CELL proliferation ,APOPTOSIS ,FISHER exact test ,IN vivo studies ,XENOGRAFTS ,CELL motility ,CELL cycle ,CHI-squared test ,MULTIVARIATE analysis ,DESCRIPTIVE statistics ,CELL lines ,CELL culture ,IMMUNOHISTOCHEMISTRY ,KAPLAN-Meier estimator ,LOG-rank test ,DRUG efficacy ,ANIMAL experimentation ,WESTERN immunoblotting ,ANALYSIS of variance ,ONE-way analysis of variance ,STATISTICS ,PROGRESSION-free survival ,DATA analysis software ,EPIDERMAL growth factor receptors ,DISEASE progression ,OVERALL survival ,REGRESSION analysis - Abstract
Background: Human epidermal growth factor receptor 2 (HER2) plays an important role in the progression of multiple solid tumors and induces resistance to epidermal growth factor receptor (EGFR) target treatment. However, the expression status and the clinical significance of HER2 in oral squamous cell carcinoma (OSCC) is still controversial. Pyrotinib (PYR) is a promising novel EGFR/HER2 dual inhibitor, whose efficacy in OSCC has not been determined. Methods: 57 locally advanced de novo OSCC patients were included in this study to investigate the relationship between the HER2 expression levels and the prognosis by the tissue microarray analysis (TMA). In vitro and in vivo experiments were performed to retrieve the efficacy of PYR in OSCC. The main downstream of HER2 was evaluated by western blotting in OSCC cell lines and xenograft tumors to explore the potential mechanism of PYR. Results: This study revealed the primary tumor of OSCC had higher HER2 expression levels. Patients with HER2 overexpression had poor overall survival (P < 0.014) and poor disease free survival (P < 0.042). In vitro, PYR suppressed the proliferation, colony formation and migration of OSCC cells. It also promoted apoptosis of OSCC cells and induced cell cycle arrest. Furthermore, PYR was able to inhibit the occurrence and development of OSCC effectively in vivo. Western blotting revealed that PYR suppressed OSCC by inhibiting the phosphorylation of HER2, AKT and ERK. Conclusions: This study exhibited the anti-OSCC effects of PYR in vitro and in vivo, and demonstrated PYR inhibited OSCC cells by inducing apoptosis via the HER2/ AKT and ERK pathway. The result of this study also indicated locally advanced OSCC patients might benefit from HER2 assay and EGFR/HER2 dual inhibit treatment. [ABSTRACT FROM AUTHOR]
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- 2024
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12. Extract of Phyllanthus emblica L. fruit stimulates basal glucose uptake and ameliorates palmitate-induced insulin resistance through AMPK activation in C2C12 myotubes.
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Li, Hai-yan, Li, Chun-fei, Liu, Chun-hui, Chen, Sun-ce, Liu, Yi-fan, Lv, Quan-he, and Zhang, Wen
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FRUIT ,MEMBRANE transport proteins ,CHINESE medicine ,SKELETAL muscle ,RESEARCH funding ,FLAVONOIDS ,HYPOGLYCEMIC agents ,AMP-activated protein kinases ,CELLULAR signal transduction ,QUANTITATIVE research ,DESCRIPTIVE statistics ,PLANT extracts ,INSULIN resistance ,BLOOD sugar ,RATS ,CELL lines ,ANIMAL experimentation ,MEDICINAL plants ,WESTERN immunoblotting ,MASS spectrometry ,ONE-way analysis of variance ,FATTY acids ,DATA analysis software ,CELL differentiation ,CELL survival ,DIABETES ,REGRESSION analysis ,PHARMACODYNAMICS - Abstract
Background: The fruit of Phyllanthus emblica L., a traditional medicine in China and India, is used to treat diabetes mellitus. Its water extract (WEPE) has demonstrated hypoglycemic effects in diabetic rats, but its mechanisms on glucose utilization and insulin resistance in skeletal muscle remain unclear. Therefore, this study aims to investigate the effects and underlying mechanisms of WEPE on glucose utilization and insulin resistance using C2C12 myotubes. Methods: Effects of WEPE on glucose uptake, GLUT4 translocation, and AMPK and AKT phosphorylation were investigated in C2C12 myotubes and palmitate-treated myotubes. An AMPK inhibitor and siRNA were used to explore the mechanisms of WEPE. Glucose uptake was determined using a 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) amino)-2-deoxyglucose (2-NBDG) uptake assay, and protein expression and GLUT4 translocation were assessed via western blotting. Results: In normal myotubes, WEPE significantly stimulated glucose uptake and GLUT4 translocation to the plasma membrane at concentrations of 125 and 250 µg/mL. This was accompanied by an increase in the phosphorylation of AMPK and its downstream targets. However, both compound C and AMPK siRNA blocked the WEPE-induced GLUT4 translocation and glucose uptake. Moreover, pretreatment with STO-609, a calcium/calmodulin-dependent protein kinase kinase β (CaMKKβ) inhibitor, inhibited WEPE-induced AMPK phosphorylation and attenuated the WEPE-stimulated glucose uptake and GLUT4 translocation. In myotubes treated with palmitate, WEPE prevented palmitate-induced insulin resistance by enhancing insulin-mediated glucose uptake and AKT phosphorylation. It also restored the insulin-mediated translocation of GLUT4 from cytoplasm to membrane. However, these effects of WEPE on glucose uptake and GLUT4 translocation were blocked by pretreatment with compound C. Conclusions: WEPE significantly stimulated basal glucose uptake though CaMKKβ/AMPK pathway and markedly ameliorated palmitate-induced insulin resistance by activating the AMPK pathway in C2C12 myotubes. [ABSTRACT FROM AUTHOR]
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- 2024
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13. Inhibition of N-acetylglucosaminyltransferase V alleviates diabetic cardiomyopathy in mice by attenuating cardiac hypertrophy and fibrosis.
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Zhao, Ran, Hu, Jianqiang, Wen, He, Zhao, Jieqiong, Wang, Ying, Niu, Xiaona, Zhang, Mingming, Wang, Tingting, and Li, Yan
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IN vitro studies ,GLUCOSE ,PROTEINS ,GLYCOSYLATION ,INTRAPERITONEAL injections ,THERAPEUTICS ,T-test (Statistics) ,DATA analysis ,STATISTICAL significance ,RESEARCH funding ,CARDIAC hypertrophy ,HEART failure ,IN vivo studies ,CELLULAR signal transduction ,PEPTIDE hormones ,DESCRIPTIVE statistics ,FLUORESCENT antibody technique ,FIBROSIS ,MICE ,PLANT extracts ,INJECTIONS ,RNA ,GENE expression ,CELL lines ,FIBROBLASTS ,IMMUNOHISTOCHEMISTRY ,DIABETIC cardiomyopathy ,ANIMAL experimentation ,MYOCARDIUM ,ATRIAL natriuretic peptides ,ONE-way analysis of variance ,STATISTICS ,WESTERN immunoblotting ,TRANSFERASES ,MOLECULAR biology ,COLLAGEN ,DATA analysis software ,COMPARATIVE studies ,OLIGOSACCHARIDES ,VIRUSES ,DIABETES ,HEART cells ,TRANSFORMING growth factors-beta ,BLOOD sugar monitoring - Abstract
Background: The pathogenesis of diabetic cardiomyopathy is closely linked to abnormal glycosylation modifications. N-acetylglucosaminyltransferase V (GnT-V), which catalyzes the production of N-linked -1–6 branching of oligosaccharides, is involved in several pathophysiological mechanisms of many disorders, including cardiac hypertrophy and heart failure. However, the mechanism by which GnT-V regulates cardiac hypertrophy in diabetic cardiomyopathy is currently poorly understood. In this study, we investigated the role of GnT-V on myocardial hypertrophy in diabetic cardiomyopathy and elucidated the underlying mechanisms. Material and methods: Streptozotocin (STZ) was intraperitoneally injected into mice to induce diabetic cardiomyopathy. An adeno-associated virus (AAV) carrying negative control small hairpin RNA (shNC) or GnT-V-specifc small hairpin RNA (shGnT-V) was used to manipulate GnT-V expression. In our study, forty male C57BL/6J mice were randomly divided into four groups (10 mice per group): control mice with AAV-shNC, diabetic cardiomyopathy mice with AAV-shNC, control mice with AAV-shGnT-V, and diabetic cardiomyopathy mice with AAV-shGnT-V. In addition, H9C2 cells and primary neonatal cardiac fibroblasts treated with high glucose were used as a cell model of diabetes. Analysis of cardiac hypertrophy and fibrosis, as well as functional studies, were used to investigate the underlying molecular pathways. Results: AAV-mediated GnT-V silencing dramatically improved cardiac function and alleviated myocardial hypertrophy and fibrosis in diabetic mice. In vitro experiments demonstrated that GnT-V was elevated in cardiomyocytes and induced cardiomyocyte hypertrophy in response to high glucose stimulation. GnT-V knockdown significantly reduced the expression of the integrinβ1 signaling pathway, as evidenced by decreased downstream ERK1/2 activity, which inhibited cardiomyocyte hypertrophy accompanied by reduced ANP, BNP, and β-MHC expression. Furthermore, knocking down GnT-V expression lowered the TGF-β1-Smads signaling pathway, which reduced the expression of α-SMA, collagen I, and collagen III. Conclusions: Overall, our research indicated that GnT-V may be a useful therapeutic target to treat diabetic cardiomyopathy, primarily in the inhibition of myocardial hypertrophy and fibrosis. [ABSTRACT FROM AUTHOR]
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- 2024
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14. Chemopreventive effect of modified zeng-sheng-ping on oral squamous cell carcinoma by regulating tumor associated macrophages through targeting tnf alpha induced protein 6.
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Wang, Jiaqi, Lin, Feiran, Zhou, Yongxiang, Cong, Yuyi, Yang, Sen, Wang, Sujuan, and Guan, Xiaobing
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RNA analysis ,SQUAMOUS cell carcinoma ,CHINESE medicine ,PROTEINS ,IN vitro studies ,COMPUTER-assisted molecular modeling ,MOUTH tumors ,MACROPHAGES ,RESEARCH funding ,LIQUID chromatography-mass spectrometry ,T-test (Statistics) ,DATA analysis ,HEAD & neck cancer ,HERBAL medicine ,ANTINEOPLASTIC agents ,FLAVONOIDS ,CELL proliferation ,IN vivo studies ,CELL motility ,DESCRIPTIVE statistics ,MICE ,CELL lines ,GENE expression ,MESSENGER RNA ,DRUG efficacy ,ANIMAL experimentation ,ONE-way analysis of variance ,STATISTICS ,CYTOKINES ,DATA analysis software ,TUMOR necrosis factors ,SEQUENCE analysis ,INTERLEUKINS ,IMMUNOSUPPRESSION ,PHARMACODYNAMICS - Abstract
Background: Oral squamous cell carcinoma (OSCC) is the most common malignancy of the head and neck. Zeng-Sheng-Ping, composed of Sophora tonkinensis Gagnep., Bistorta officinalis Delarbre, Sonchus arvensis L., Prunella vulgaris L., Dioscorea bulbifera L., and Dictamnus dasycarpus Turcz., was regarded as an anti-cancer drug with significant clinical efficacy, but was discontinued due to liver toxicity. Our research group developed a modified Zeng-Sheng-Ping (ZSP-M) based on original Zeng-Sheng-Ping that exhibited high efficiency and low toxicity in preliminary investigations, although its pharmacodynamic mechanism is still unclear. Here, we aimed to elucidate the pharmacodynamic material basis of ZSP-M and investigate its chemopreventive effect on OSCC by modulating tumor associated macrophages (TAMs). Methods: Components of ZSP-M were characterized using ultra-performance liquid chromatography-mass spectrometry. Chemopreventive effect induced by ZSP-M against experimental oral cancer was investigated using the 4-nitroquinoline N-oxide precancerous lesion mouse model. RNA sequencing analysis was used to gain a global transcriptional view of the effect of ZSP-M treatment. A cell co-culture model was used to study the targeted effect of ZSP-M on TAMs and the biological properties of OSCC cells and to detect changes in TAM phenotypes. The binding of ZSP-M active compounds to TNF alpha induced protein 6 (TNFAIP6) protein was analyzed by molecular docking and dynamic simulation. Results: Forty main components of ZSP-M were identified, the most abundant of which were flavonoids. ZSP-M inhibited the degree of epithelial dysplasia in precancerous lesions by inhibiting the expression of the TNFAIP6 and CD163 proteins in the precancerous lesions of the tongue. ZSP-M inhibited proliferation, colony formation, migration and invasion of SCC7 cells by targeting TAMs. ZSP-M reduced the expression of CD163
+ cells, inhibited the expression of TNFAIP6 protein, Arg1 mRNA and Il10 mRNA in TAMs, and reduced IL-10 cytokine release in the co-culture environment. This effect was maintained after the addition of recombinant TNFAIP6 protein. Computer simulations showed that trifolirhizin and maackiain are well-connected to TNFAIP6. Conclusions: ZSP-M counteracts the immunosuppressive action of TAMs by specific targeting of TNFAIP6, thereby exerting chemopreventive activity of OSCC. [ABSTRACT FROM AUTHOR]- Published
- 2024
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15. PARP4 interacts with hnRNPM to regulate splicing during lung cancer progression.
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Lee, Yi Fei, Phua, Cheryl Zi Jin, Yuan, Ju, Zhang, Bin, Lee, May Yin, Kannan, Srinivasaraghavan, Chiu, Yui Hei Jasper, Koh, Casslynn Wei Qian, Yap, Choon Kong, Lim, Edwin Kok Hao, Chen, Jianbin, Lim, Yuhua, Lee, Jane Jia Hui, Skanderup, Anders Jacobsen, Wang, Zhenxun, Zhai, Weiwei, Tan, Nguan Soon, Verma, Chandra S., Tay, Yvonne, and Tan, Daniel Shao Weng
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LUNG cancer ,RNA splicing ,CANCER invasiveness ,CANCER genes ,NON-small-cell lung carcinoma ,CELL lines - Abstract
Background: The identification of cancer driver genes from sequencing data has been crucial in deepening our understanding of tumor biology and expanding targeted therapy options. However, apart from the most commonly altered genes, the mechanisms underlying the contribution of other mutations to cancer acquisition remain understudied. Leveraging on our whole-exome sequencing of the largest Asian lung adenocarcinoma (LUAD) cohort (n = 302), we now functionally assess the mechanistic role of a novel driver, PARP4. Methods: In vitro and in vivo tumorigenicity assays were used to study the functional effects of PARP4 loss and mutation in multiple lung cancer cell lines. Interactomics analysis by quantitative mass spectrometry was conducted to identify PARP4's interaction partners. Transcriptomic data from cell lines and patient tumors were used to investigate splicing alterations. Results: PARP4 depletion or mutation (I1039T) promotes the tumorigenicity of KRAS- or EGFR-driven lung cancer cells. Disruption of the vault complex, with which PARP4 is commonly associated, did not alter tumorigenicity, indicating that PARP4's tumor suppressive activity is mediated independently. The splicing regulator hnRNPM is a potentially novel PARP4 interaction partner, the loss of which likewise promotes tumor formation. hnRNPM loss results in splicing perturbations, with a propensity for dysregulated intronic splicing that was similarly observed in PARP4 knockdown cells and in LUAD cohort patients with PARP4 copy number loss. Conclusions: PARP4 is a novel modulator of lung adenocarcinoma, where its tumor suppressive activity is mediated not through the vault complex—unlike conventionally thought, but in association with its novel interaction partner hnRNPM, thus suggesting a role for splicing dysregulation in LUAD tumorigenesis. [ABSTRACT FROM AUTHOR]
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- 2024
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16. Photoactive metabolite mediated photodynamic therapy of Rhabdomyosarcoma cell lines using medicinal plants and Doxorubicin co-treatments.
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Javaid, Sumbal, Qureshi, Irfan Zia, Khurshid, Ahmat, Afsar, Tayyaba, Husain, Fohad Mabood, Khurshid, Muhammad, Trembley, Janeen H., and Razak, Suhail
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PHYTOTHERAPY ,PHARMACEUTICAL arithmetic ,PHOTOSENSITIZERS ,QUALITATIVE research ,DATA analysis ,RESEARCH funding ,ANTINEOPLASTIC agents ,ETHANOL ,DESCRIPTIVE statistics ,TREATMENT effectiveness ,QUANTITATIVE research ,CELL lines ,PLANT extracts ,METABOLITES ,CYTOTOXINS ,CANCER chemotherapy ,REACTIVE oxygen species ,DOXORUBICIN ,SPECTRUM analysis ,CELL death ,DRUG interactions ,ONE-way analysis of variance ,STATISTICS ,RHABDOMYOSARCOMA ,PHOTODYNAMIC therapy ,FACTOR analysis ,CELL survival ,COMPARATIVE studies ,DATA analysis software ,MICROSCOPY ,HEALTH care teams ,SPECTROPHOTOMETRY ,EVALUATION - Abstract
Background: Medicinal plant-mediated combinational therapies have gained importance globally due to minimal side effects and enhanced treatment outcomes compared to single-drug modalities. We aimed to analyze the cytotoxic potential of each conventional treatment i.e., photodynamic therapy (PDT), chemotherapy (doxorubicin hydrochloride; Dox-HCl) with or without various concentrations of medicinal plant extracts (PE) on soft tissue cancer Rhabdomyosarcoma (RD) cell line. Methods: The Rhabdomyosarcoma (RD) cell line was cultured and treated with Photosensitizer (Photosense (AlPc4)), Chemo (Dox-HCl), and their combinations with different concentrations of each plant extract i.e., Thuja occidentalis, Moringa oleifera, Solanum surattense. For the source of illumination, a Diode laser (λ = 630 nm ± 1 nm, P
max = 1.5 mW) was used. Photosensitizer uptake time (∼ 45 min) was optimized through spectrophotometric measurements (absorption spectroscopy). Drug response of each treatment arm was assessed post 24 h of administration using 3-(4, 5-dimethyl-2-thiazolyl)-2, 5- 5-diphenyl-2 H- tetrazolium bromide (MTT) assay. Results: PE-mediated Chemo-Photodynamic therapy (PDT) exhibited synergistic effects (CI < 1). Moreover, Rhabdomyosarcoma culture pretreated with various plant extracts for 24 h exhibited significant inhibition of cell viability however most effective outcomes were shown by low and high doses of Moringa oleifera compared to other plant extracts. Post low doses treated culture with all plant extracts followed by PDT came up with more effectiveness when compared to all di-therapy treatments. Conclusion: The general outcome of this work shows that the ethanolic plant extracts (higher doses) promote the death of cancerous cells in a dose-dependent way and combining Dox-HCl and photo-mediated photodynamic therapy can yield better therapeutic outcomes. [ABSTRACT FROM AUTHOR]- Published
- 2024
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17. Kalanchoe pinnata (Lam.) Pers. Leaf ethanolic extract exerts selective anticancer activity through ROS-induced apoptotic cell death in human cancer cell lines.
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Faundes-Gandolfo, Nicolas, Jara-Gutiérrez, Carlos, Párraga, Mario, Montenegro, Iván, Vera, Waleska, Escobar, Marcela, Madrid, Alejandro, Valenzuela-Valderrama, Manuel, and Villena, Joan
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IN vitro studies ,MITOCHONDRIAL membranes ,RESEARCH funding ,DATA analysis ,ANTINEOPLASTIC agents ,APOPTOSIS ,FLAVONOIDS ,ETHANOL ,PHYTOCHEMICALS ,DESCRIPTIVE statistics ,PLANT extracts ,REACTIVE oxygen species ,CELL lines ,COLON tumors ,GAS chromatography ,CELL death ,ANTIOXIDANTS ,HYDROGEN peroxide ,ONE-way analysis of variance ,STATISTICS ,LEAVES ,CASPASES ,PHARMACODYNAMICS - Abstract
Background: The leaves of Kalanchoe pinnata (Lam.) Pers. (K. pinnata), a succulent plant native to tropical regions, are used as a medicinal alternative against cancer in several countries worldwide; however, its therapeutic potential to fight cancer has been little addressed. In this study, we analyzed the phytochemical content, antioxidant capacity, and selectivity of K. pinnata leaf ethanolic extract against different human cancer cell lines in vitro. Methodology: This study subjected the ethanolic extract to enzymatic assays to quantify the phytochemical content (phenolics, flavonoids, and anthraquinones) and its radical scavenging and iron-reducing capacities. Also, the phytoconstituents and major phenolic compounds present in the extract's subfractions were identified by GC-MS, HPLC, and NMR. Human cancer (MCF-7, PC-3, HT-29) and normal colon (CoN) cell lines were treated with different concentrations of K. pinnata leaf ethanolic extract, and the changes in cell proliferation (sulforhodamine B assay), caspases activity (FITC-VAD-FMK reporter), mitochondrial membrane potential (MMP, rhodamine 123 assay), chromatin condensation/fragmentation (Hoechst 33342 stain), and ROS generation (DCFH
2 probe assay) were assessed. Results: The results showed that the K. pinnata leaf ethanolic extract is rich in phytoconstituents with therapeutic potential, including phenols (quercetin and kaempferol), flavonoids, fatty acid esters (34.6% of the total composition), 1- triacontanol and sterols (ergosterol and stigmasterol, 15.4% of the total composition); however, it presents a poor content of antioxidant molecules (IC50 = 27.6 mg/mL for H2 O2 scavenging activity vs. 2.86 mg/mL in the case of Trolox). Notably, the extract inhibited cell proliferation and reduced MMP in all human cell lines tested but showed selectivity for HT-29 colon cancer cells compared to CoN normal cells (SI = 8.4). Furthermore, ROS generation, caspase activity, and chromatin condensation/fragmentation were augmented significantly in cancer-derived cell lines, indicating a selective cytotoxic effect. Conclusion: These findings reveal that the K. pinnata leaf ethanolic extract contains several bioactive molecules with therapeutic potential, capable of displaying selective cytotoxicity in different human cancer cell lines. [ABSTRACT FROM AUTHOR]- Published
- 2024
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18. Effects of essential oil of Origanum onites and its major component carvacrol on the expression of toxicity pathway genes in HepG2 cells.
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Tomsuk, Özlem, Kuete, Victor, Sivas, Hülya, and Kürkçüoğlu, Mine
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DNA analysis ,HEPATOTOXICOLOGY ,T-test (Statistics) ,RESEARCH funding ,ESSENTIAL oils ,TERPENES ,CHALONES ,ANTINEOPLASTIC agents ,CELL proliferation ,POLYMERASE chain reaction ,CELLULAR signal transduction ,PLANT extracts ,GENE expression ,EXPERIMENTAL design ,CELL lines ,REACTIVE oxygen species ,PHENOLS ,MOLECULAR structure ,ONE-way analysis of variance ,DATA analysis software ,HEPATOCELLULAR carcinoma ,SEQUENCE analysis ,PHARMACODYNAMICS - Abstract
Background: Origanum species have been used in various commercial constructions as a remedy against burns and wounds, agriculture, alcoholic drinks, fragrance, and flavoring substances of food products. The essential oil of Origanum onites L. (EOOO) and its component carvacrol (CV) possesses a wide range of biological activities including anti-cancer activity. Purpose: The purpose of this study was to investigate the growth inhibitory activity of the essential oil and its major component CV and then hepatotoxicity pathway-related genes in HepG2 cells. Methods: The effects of the EOOO and CV on cell growth and mRNA expressions of 84 hepatotoxicity pathway-related genes were investigated in HepG2, using trypan blue exclusion/ bromodeoxyuridine (BrdU) incorporation tests and real-time-polymerase chain reaction (RT-PCR) array, respectively. Results: The EOOO and CV inhibited cell growth with IC
50 values of 0.08 µg/mL and 45 µg/mL, respectively, after 24 h. Real-time, reverse-transcription-polymerase chain reaction (RT2 -PCR) array analysis revealed that expressions of 32 genes out of 84 were changed at least 2-fold or more in the EOOO-treated cells. Among them, expression levels of 17 genes were elevated, while expression levels of 15 genes were diminished. Furthermore, after exposure of cells to 45 µg/mL of CV, the expression of 8 genes was increased while the other 8 genes were decreased. Both the EOOO and carvacrol affected the expression of 48 genes of HepG2 cells which are involved in the hepatotoxicity pathway, indicating their hepatoprotective and possible anti-hepatocarcinogenic effects. Conclusion: The present study demonstrates that the essential oil of Origanum onites and carvacrol can be used in various applications such as anticancer or herbal drugs, since its non-hepatotoxicity. [ABSTRACT FROM AUTHOR]- Published
- 2024
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19. Isolation and anti-neuroinflammation activity of sesquiterpenoids from Artemisia argyi: computational simulation and experimental verification.
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La, Caiwenjie, Li, Menghe, Wang, Zexu, Liu, Tao, Zeng, Qiongzhen, Sun, Pinghua, Ren, Zhe, Ye, Cuifang, Liu, Qiuying, and Wang, Yifei
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FOLIAR diagnosis ,COMPUTER-assisted molecular modeling ,MITOGEN-activated protein kinases ,NF-kappa B ,HIGH performance liquid chromatography ,NITRIC oxide ,PROTEIN kinases ,PHOSPHORYLATION ,NUCLEAR magnetic resonance spectroscopy ,COMPUTER software ,COLORIMETRY ,RESEARCH funding ,TERPENES ,POLYMERASE chain reaction ,NEUROGLIA ,ENZYME-linked immunosorbent assay ,NEUROINFLAMMATION ,CELLULAR signal transduction ,JANUS kinases ,MICE ,CELL lines ,CELL culture ,MEDICINAL plants ,ANIMAL experimentation ,SPECTRUM analysis ,WESTERN immunoblotting ,MATRIX metalloproteinases ,BOTULINUM toxin ,LIPOPOLYSACCHARIDES ,STAT proteins ,CHROMATOGRAPHIC analysis ,EPIDERMAL growth factor receptors ,ANALYTICAL chemistry ,CELL receptors - Abstract
Background: Artemisia argyi is a traditional herbal medicine belonging to the genus Artemisia that plays an important role in suppressing inflammation. However, the chemical constituents and underlying mechanisms of its therapeutic potential in neuroinflammation are still incompletely understood, and warrant further investigation. Methods: Several column chromatography were employed to isolate and purify chemical constituents from Artemisia argyi, and modern spectroscopy techniques were used to elucidate their chemical structures. The screening of monomeric compounds with nitric oxide inhibition led to the identification of the most effective bioactive compound, which was subsequently confirmed for its anti-inflammatory capability through qRT‒PCR. Predictions of compound-target interactions were made using the PharmMapper webserver and the TargetNet database, and an integrative protein-protein interaction network was constructed by intersecting the predicted targets with neuroinflammation-related targets. Topological analysis was performed to identify core targets, and molecular docking and molecular dynamics simulations were utilized to validate the findings. The result of the molecular simulations was experimentally validated through drug affinity responsive target stability (DARTS) and Western blot experiments. Results: Seventeen sesquiterpenoids, including fifteen known sesquiterpenoids and two newly discovered guaiane-type sesquiterpenoids (argyinolide S and argyinolide T) were isolated from Artemisia argyi. Bioactivity screening revealed that argyinolide S (AS) possessed the most potent anti-inflammatory activity. However, argyinolide T (AT) showed weak anti-inflammatory activity, so AS was the target compound for further study. AS may regulate neuroinflammation through its modulation of eleven core targets: protein kinase B 1 (AKT1), epidermal growth factor receptor (EGFR), proto-oncogene tyrosine-protein Kinase (FYN), Janus Kinase (JAK) 1, mitogen-activated protein (MAP) Kinase 1,8 and 14, matrix metalloproteinase 9 (MMP9), ras-related C3 botulinum toxin substrate 1 (RAC1), nuclear factor kappa-B p65 (RELA), and retinoid X receptor alpha (RXRA). Molecular dynamics simulations and DARTS experiments confirmed the stable binding of AS to JAK1, and Western blot experiments demonstrated the ability of AS to inhibit the phosphorylation of downstream Signal transducer and activator of transcription 3 (STAT3) mediated by JAK1. Conclusions: The sesquiterpenoid compounds isolated from Artemisia argyi, exhibit significant inhibitory effects on inflammation in C57BL/6 murine microglia cells (BV-2). Among these compounds, AS, a newly discovered guaiane-type sesquiterpenoid in Artemisia argyi, has been demonstrated to effectively inhibit the occurrence of neuroinflammation by targeting JAK1. [ABSTRACT FROM AUTHOR]
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- 2024
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20. A positive feedback loop between PFKP and c-Myc drives head and neck squamous cell carcinoma progression.
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Liu, Weiwei, Ding, Zhao, Tao, Ye, Liu, Shixian, Jiang, Maoyu, Yi, Fangzheng, Wang, Zixi, Han, Yanxun, Zong, Huaiyuan, Li, Dapeng, Zhu, Yue, Xie, Zihui, Sang, Shujia, Chen, Xixi, Miao, Manli, Chen, Xu, Lin, Wei, Zhao, Yi, Zheng, Guibin, and Zafereo, Mark
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SQUAMOUS cell carcinoma ,TREATMENT effectiveness ,HEAD & neck cancer ,NECK ,CELL proliferation ,CELL lines - Abstract
Background: The aberrant expression of phosphofructokinase-platelet (PFKP) plays a crucial role in the development of various human cancers by modifying diverse biological functions. However, the precise molecular mechanisms underlying the role of PFKP in head and neck squamous cell carcinoma (HNSCC) are not fully elucidated. Methods: We assessed the expression levels of PFKP and c-Myc in tumor and adjacent normal tissues from 120 HNSCC patients. A series of in vitro and in vivo experiments were performed to explore the impact of the feedback loop between PFKP and c-Myc on HNSCC progression. Additionally, we explored the therapeutic effects of targeting PFKP and c-Myc in HNSCC using Patient-Derived Organoids (PDO), Cell Line-Derived Xenografts, and Patients-Derived Xenografts. Results: Our findings indicated that PFKP is frequently upregulated in HNSCC tissues and cell lines, correlating with poor prognosis. Our in vitro and in vivo experiments demonstrate that elevated PFKP facilitates cell proliferation, angiogenesis, and metastasis in HNSCC. Mechanistically, PFKP increases the ERK-mediated stability of c-Myc, thereby driving progression of HNSCC. Moreover, c-Myc stimulates PFKP expression at the transcriptional level, thus forming a positive feedback loop between PFKP and c-Myc. Additionally, our multiple models demonstrate that co-targeting PFKP and c-Myc triggers synergistic anti-tumor effects in HNSCC. Conclusion: Our study demonstrates the critical role of the PFKP/c-Myc positive feedback loop in driving HNSCC progression and suggests that simultaneously targeting PFKP and c-Myc may be a novel and effective therapeutic strategy for HNSCC. [ABSTRACT FROM AUTHOR]
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- 2024
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21. Effects and mechanisms of puerarin against neuroblastoma: insights from bioinformatics and in vitro experiments.
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Sui, Xiaohui, Liu, Tingting, Zou, Zhiyun, Zhang, Baoqing, and Zhang, Guiju
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THERAPEUTIC use of isoflavones ,PHYTOTHERAPY ,CHINESE medicine ,IN vitro studies ,RISK assessment ,PHARMACOLOGY ,WOUND healing ,MITOCHONDRIAL membranes ,PREDICTION models ,ISOFLAVONES ,CELL proliferation ,POLYMERASE chain reaction ,TREATMENT effectiveness ,FLUORESCENT antibody technique ,CELL motility ,QUANTITATIVE research ,DESCRIPTIVE statistics ,METASTASIS ,BIOINFORMATICS ,GENE expression ,CELL lines ,CELL culture ,WESTERN immunoblotting ,ONE-way analysis of variance ,CELL survival ,DATA analysis software ,NEUROBLASTOMA ,REGRESSION analysis ,MITOCHONDRIAL DNA ,CHILDREN - Abstract
Background: Neuroblastoma, a prevalent solid tumor in children, often manifests with hidden onset sites, rapid growth, and high metastatic potential. The prognosis for children with high-risk neuroblastoma remains poor, highlighting the urgent need for novel prognostic models and therapeutic avenues. In recent years, puerarin, as a kind of small molecule drug extracted from Chinese medicine Pueraria lobata, has demonstrated significant anticancer effects on various cancer cell types. In this study, through bioinformatics analysis and in vitro experiments, the potential and mechanism of puerarin in the treatment of neuroblastoma were investigated, and a prognostic model was established. Methods: A total of 9 drug-disease related targets were observed by constructing a database of drug targets and disease genes. Besides, GO and KEGG enrichment analysis was performed to explore the potential mechanism of its therapeutic effect. To construct the prognostic model, risk regression analysis and LASSO analysis were carried out for validation. Finally, the prognostic genes were identified. Parachute test and immunofluorescence staining were performed to verify the potential mechanism of puerarin in neuroblastoma treatment. Results: Three prognostic genes, i.e., BIRC5, TIMP2 and CASP9, were identified. In vitro studies verified puerarin's impact on BIRC5, TIMP2, and CASP9 expression, inhibiting proliferation in neuroblastoma SH-SY5Y cells. Puerarin disrupts the cytoskeleton, boosts gap junctional communication, curtailing invasion and migration, and induces mitochondrial damage in SH-SY5Y cells. Conclusions: Based on network pharmacology and bioinformatics analysis, combined with in vitro experimental verification, puerarin was hereby observed to enhance GJIC in neuroblastoma, destroy cytoskeleton and thus inhibit cell invasion and migration, cause mitochondrial damage of tumor cells, and inhibit cell proliferation. Overall, puerarin, as a natural medicinal compound, does hold potential as a novel therapy for neuroblastoma. [ABSTRACT FROM AUTHOR]
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- 2024
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22. Establishment and characterization of a novel multidrug-resistant pancreatic ductal adenocarcinoma cell line, PDAC-X1.
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Yu, Cheng, Su, Yuanhui, Miao, Xin, Chai, Changpeng, Tang, Huan, Li, Lu, Yi, Jianfeng, Ye, Zhenzhen, Zhang, Hui, Hu, Zhao, Chen, Luyang, Li, Ning, Xu, Hao, and Zhou, Wence
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PANCREATIC duct ,CELL lines ,ORGAN culture ,CELL morphology ,MULTIDRUG resistance - Abstract
Drug resistance remains a significant challenge in the treatment of pancreatic cancer. The development of drug-resistant cell lines is crucial to understanding the underlying mechanisms of resistance and developing novel drugs to improve clinical outcomes. Here, a novel pancreatic cancer cell line, PDAC-X1, derived from Chinese patients has been established. PDAC-X1 was characterized by the immune phenotype, biology, genetics, molecular characteristics, and tumorigenicity. In vitro analysis revealed that PDAC-X1 cells exhibited epithelial morphology and cell markers (CK7 and CK19), expressed cancer-associated markers (E-cadherin, Vimentin, Ki-67, CEA, CA19-9), and produced pancreatic cancer-like organs in suspension culture. In vivo analysis showed that PDAC-X1 cells maintained tumorigenicity with a 100% tumor formation rate. This cell line exhibited a complex karyotype, dominated by subtriploid karyotypes. In addition, PDAC-X1 cells exhibited intrinsic multidrug resistance to multiple drugs, including gemcitabine, paclitaxel, 5-fluorouracil, and oxaliplatin. In conclusion, the PDAC-X1 cell line has been established and characterized, representing a useful and valuable preclinical model to study the underlying mechanisms of drug resistance and develop novel drug therapeutics to improve patient outcomes. [ABSTRACT FROM AUTHOR]
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- 2024
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23. Phytotherapeutic potential against MRSA: mechanisms, synergy, and therapeutic prospects.
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He, Qiqi, Meneely, Julie, Grant, Irene R., Chin, Jason, Fanning, Séamus, and Situ, Chen
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ANTIBIOTICS ,CHINESE medicine ,CLINICAL drug trials ,ADENOCARCINOMA ,STAPHYLOCOCCAL diseases ,PATIENT safety ,HERBAL medicine ,ELECTRON microscopy ,METHICILLIN-resistant staphylococcus aureus ,COLORECTAL cancer ,PLANT extracts ,CELL lines ,DOSE-effect relationship in pharmacology ,MEDICINAL plants ,DRUG development ,CELL survival ,DRUG synergism ,HEPATOCELLULAR carcinoma ,PHARMACODYNAMICS - Abstract
Background: Rising resistance to antimicrobials, particularly in the case of methicillin-resistant Staphylococcus aureus (MRSA), represents a formidable global health challenge. Consequently, it is imperative to develop new antimicrobial solutions. This study evaluated 68 Chinese medicinal plants renowned for their historical applications in treating infectious diseases. Methods: The antimicrobial efficacy of medicinal plants were evaluated by determining their minimum inhibitory concentration (MIC) against MRSA. Safety profiles were assessed on human colorectal adenocarcinoma (Caco-2) and hepatocellular carcinoma (HepG2) cells. Mechanistic insights were obtained through fluorescence and transmission electron microscopy (FM and TEM). Synergistic effects with vancomycin were investigated using the Fractional Inhibitory Concentration Index (FICI). Results: Rheum palmatum L., Arctium lappa L. and Paeonia suffructicosaas Andr. have emerged as potential candidates with potent anti-MRSA properties, with an impressive low MIC of 7.8 µg/mL, comparable to the 2 µg/mL MIC of vancomycin served as the antibiotic control. Crucially, these candidates demonstrated significant safety profiles when evaluated on Caco-2 and HepG2 cells. Even at 16 times the MIC, the cell viability ranged from 83.3% to 95.7%, highlighting their potential safety. FM and TEM revealed a diverse array of actions against MRSA, such as disrupting the cell wall and membrane, interference with nucleoids, and inducing morphological alterations resembling pseudo-multicellular structures in MRSA. Additionally, the synergy between vancomycin and these three plant extracts was evident against MRSA (FICI < 0.5). Notably, aqueous extract of R. palmatum at 1/4 MIC significantly reduced the vancomycin MIC from 2 µg/mL to 0.03 µg/mL, making a remarkable 67-fold decrease. Conclusions: This study unveil new insights into the mechanistic actions and pleiotropic antibacterial effectiveness of these medicinal plants against resistant bacteria, providing robust evidence for their potential use as standalone or in conjunction with antibiotics, to effectively combat antimicrobial resistance, particularly against MRSA. [ABSTRACT FROM AUTHOR]
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- 2024
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24. MiR-18a affects hypoxia induced glucose metabolism transition in HT22 hippocampal neuronal cell line through the Hif1a gene.
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Liu, Chuncheng, Liu, Gehui, Zuo, Xinyang, Qu, Donghui, Sun, Yefeng, Liu, Linan, Zhao, Xiujuan, Li, Jun, and Cai, Lu
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GLUCOSE metabolism ,NEUROLOGICAL disorders ,CELL lines ,HYPOXEMIA ,HYPOXIA-inducible factors ,WARBURG Effect (Oncology) ,HYPOXIA-inducible factor 1 - Abstract
Hypoxia can cause a variety of diseases, including ischemic stroke and neurodegenerative diseases. Within a certain range of partial pressure of oxygen, cells can respond to changes in oxygen. Changes in oxygen concentration beyond a threshold will cause damage or even necrosis of tissues and organs, especially for the central nervous system. Therefore, it is very important to find appropriate measures to alleviate damage. MiRNAs can participate in the regulation of hypoxic responses in various types of cells. MiRNAs are involved in regulating hypoxic responses in many types of tissues by activating the hypoxia-inducible factor (HIF) to affect angiogenesis, glycolysis and other biological processes. By analyzing differentially expressed miRNAs in hypoxia and hypoxia-related studies, as well as the HT22 neuronal cell line under hypoxic stress, we found that the expression of miR-18a was changed in these models. MiR-18a could regulate glucose metabolism in HT22 cells under hypoxic stress by directly regulating the 3'UTR of the Hif1a gene. As a small molecule, miRNAs are easy to be designed into small nucleic acid drugs, so this study can provide a theoretical basis for the research and treatment of nervous system diseases caused by hypoxia. [ABSTRACT FROM AUTHOR]
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- 2024
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25. Navel orange peel essential oil inhibits the growth and progression of triple negative breast cancer.
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Yang, Chao, Zhang, Wenwen, Xiang, Shi, Chen, Lai, Chun, Jiong, and Chen, Hui
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RESEARCH funding ,BREAST tumors ,ESSENTIAL oils ,CELL physiology ,APOPTOSIS ,CELL proliferation ,POLYMERASE chain reaction ,ANTINEOPLASTIC agents ,TREATMENT effectiveness ,CELLULAR signal transduction ,DESCRIPTIVE statistics ,PLANT extracts ,GENE expression ,CELL lines ,MICE ,RNA ,ANIMAL experimentation ,WESTERN immunoblotting ,COMPARATIVE studies ,ORANGES ,SEQUENCE analysis - Abstract
Background: Triple Negative Breast Cancer (TNBC) is a particular type of breast cancer with the highest mortality rate. Essential oils are concerned more and more as potential anti-cancer drugs. Methods: TNBC cells were treated with different concentrations of navel orange peel essential oil (NOPEO), and then a variety of experiments were performed to investigate the changes in the growth and progression of TNBC cells. MTT assay was performed to detect the proliferation of TNBC cells. The changes of cell cycle and apoptosis were analyzed by FACS. In order to explored the migration of TNBC cells, scratch wound assay was carried out. Western blotting and qPCR were used to examine the expression of proteins and mRNA of related genes. Furthermore, RNA-seq was used to analyze the altered genes and explored the possible signal pathway. Results: NOPEO demonstrated dose- and time-dependent suppression of TNBC cell growth. TNBC cells showed an increased percentage of G2/M-phase cells and the protein levels of CyclinB1 and CyclinD1 were decreased after NOPEO treatment. The apoptotic cells were increased in the NOPEO treated TNBC cells. The migration mobility was significantly inhibited by NOPEO. In total, 1376 genes were found to be up-regulated and 1335 genes were down-regulated after NOPEO treatment. According to KEGG and GO pathways, the differentially expressed genes were related to MAPK, Jak/stat and FoxQ signaling pathways. Conclusion: This investigation explored the bio-activity and molecular mechanisms of NOPEO against TNBC cells. These results indicated that NOPEO could suppress TNBC growth and migration perhaps via the MAPK and Jak/stat signaling pathways, which may provide theoretical reference for anticancer drug development. NOPEO may be a potential natural product for the chemotherapeutic of TNBC. [ABSTRACT FROM AUTHOR]
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- 2024
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26. Shaoyao Decoction reduced T lymphocyte activation by regulating of intestinal flora and 5-hydroxytryptamine metabolism in ulcerative colitis.
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Zhen, Jianhua, Li, Yini, Zhang, Yunan, Zhou, Yali, Zhao, Lu, Huang, Guangrui, and Xu, Anlong
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DIARRHEA ,CHINESE medicine ,NF-kappa B ,T cells ,LIQUID chromatography-mass spectrometry ,RESEARCH funding ,HERBAL medicine ,GUT microbiome ,ANIMALS ,POLYMERASE chain reaction ,ENZYME-linked immunosorbent assay ,ULCERATIVE colitis ,DNA ,CELLULAR signal transduction ,PLANT extracts ,MICE ,IMMUNOHISTOCHEMISTRY ,CELL lines ,ANIMAL experimentation ,WESTERN immunoblotting ,SEROTONIN ,METABOLOMICS ,SEQUENCE analysis - Abstract
Background: Shaoyao Decoction (SYD) is a widely recognized herbal formula utilized in traditional Chinese medicine for the treatment of diarrhea. Although it has demonstrated significant effectiveness in clinical practice for treating ulcerative colitis, the precise mechanisms by which it operates remain largely elusive. Methods: The active ingredients of SYD were obtained by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS), which were used to explore the potential pharmacological mechanism based on TCMSP (Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform) and PANTHER (Protein Analysis Through Evolutionary Relationships) classification system. In a mouse model of dextran sulfate sodium (DSS)-induced colitis, mRNA sequencing, 16S rDNA sequencing and targeted metabolomics techniques were used to elucidate the mechanisms of SYD, and immunohistochemistry, immunofluorescence, enzyme linked immunosorbent assay, real time quantitative polymerase chain reaction and western blot were used to test the key targets. In addition, QGP-1 and H9 cells were performed to validate the discoveries from the animal experiments. Results: In the mouse model of DSS-induced colitis, SYD effectively alleviated symptoms such as bloody stool, tissue damage, inflammation, intestinal flora dysbiosis and abnormal gene expression. Analyses of both differential expressed genes in colonic tissue and predicted 16S rDNA genes, as well as the analyses of targeted genes from TCMSP based on the active ingredients in UPLC-MS/MS of SYD, uncovered the enrichment of pathways involved in the biosynthesis and degredation of 5-hydroxytryptamine (5-HT). Interestingly, SYD suppressed the relative abundance of key genes in 5-HT synthesis, Tph1(Tryptophan hydroxylase 1) and Ddc (Dopa decarboxylase), in faeces from DSS-induced mice, leading to a reduction in the concentration of fecal 5-HT. Moreover, SYD augmented the production of butyric acid. Subsequently, increasing butyric acid influenced the metabolism of 5-HT in the organism through G protein-coupled receptor 43 by impeding its synthesis, facilitating its transport and degredation. These findings were additionally corroborated in a model utilizing enterochromaffin cell (QGP-1 cells). Furthermore, reduced levels of 5-HT hindered the activation of T lymphocytes (H9 cells) via the PKC (Protein kinase C) and NF-κB (Nuclear factor kappa-B) signaling pathways, by means of HTR1A (5-HT receptor 1A) and HTR3 (5-HT receptor 3). Additionally, diminished secretion of 5-HT resulted in reduced secretion of associated cytokines, thereby alleviating inflammation in the colon. Conclusion: Through modulation of T lymphocyte activation mediated by 5-HT metabolism in the local colon via the intestinal flora and its metabolite, SYD effectively mitigated colonic inflammation in DSS-induced mice. [ABSTRACT FROM AUTHOR]
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- 2024
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27. Citral in lemon myrtle, lemongrass, litsea, and melissa essential oils suppress the growth and invasion of breast cancer cells.
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Nagata, Takuya, Satou, Tadaaki, Hayashi, Shinichiro, Satyal, Prabodh, Watanabe, Manabu, Riggs, Brannick, and Saida, Yoshihisa
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THERAPEUTIC use of antineoplastic agents ,DATA analysis ,RESEARCH funding ,ESSENTIAL oils ,BREAST tumors ,CELL proliferation ,CHALONES ,APOPTOSIS ,IMMUNODIAGNOSIS ,CELL motility ,PLANT extracts ,CELL lines ,CELL culture ,GAS chromatography ,ONE-way analysis of variance ,STATISTICS ,LEMONGRASS ,BIOLOGICAL assay ,DATA analysis software ,COMPARATIVE studies ,LEMON balm ,CELL surface antigens - Abstract
Objective: Although cancer therapy suppresses recurrence and prolongs life, it may be accompanied by strong side effects; thus, there is a strong demand for the development effective treatments with fewer side effects. Cancer therapy using plant-derived essential oils is attracting attention as one promising method. This study investigated the antitumor effects of essential oil volatiles on breast cancer cells and identifies four essential oils that display antitumor activity. Methods: Breast cancer cells were cultured in a 96-well plate, then one of twenty essential oils was added dropwise to the central well. The plate was incubated at 37 °C for 48 h and the effect of the volatile components of each essential oil on the surrounding breast cancer cell growth ability was examined using an MTT assay. Gas chromatography was used to investigate the concentration of the transpiration components that may affect cancer cells. Results: Of the 20 essential oils, Lemongrass, Lemon myrtle, Litsea, and Melissa displayed strong anti-tumor effects. These essential oils inhibited the growth of nearby breast cancer cells, even when diluted more than 500-fold. The transpiration component of lemon Myrtle showed the strongest antitumor effect, but was the least cytotoxic to mononuclear cells in normal peripheral blood (PBMC). Each of these essential oils contained a very large amount of citral. The IC
50 against breast cancer cells when citral was volatilized from each essential oil was 1.67 µL/mL for geranial and 1.31 µL/mL for neral. Volatilized citral alone showed strong anti-proliferation and infiltration-inhibiting effects. Conclusion: The transpiration components of Lemongrass, Lemon myrtle, Litsea, and Melissa are thought to inhibit breast cancer cell proliferation due to their high levels of citral. [ABSTRACT FROM AUTHOR]- Published
- 2024
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28. Ethanolic extract from Sophora moorcroftiana inhibit cell proliferation and alter the mechanical properties of human cervical cancer.
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Guo, Manli, Guo, Dingcheng, Liao, Lingzi, Zhang, Xiao, Wang, Zhilong, Zhou, Qiaozhen, Chen, Ping, Li, Ruiping, Han, Bing, Bao, Guangjie, and Zhang, Baoping
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BIOMECHANICS ,FLOW cytometry ,CERVIX uteri tumors ,T-test (Statistics) ,RESEARCH funding ,ETHANOL ,CELL proliferation ,APOPTOSIS ,PLANT extracts ,CELL lines ,EXPERIMENTAL design ,BIOINFORMATICS ,GENE expression ,MASS spectrometry ,WESTERN immunoblotting ,PROTEOMICS ,ELECTROPHORESIS ,CASPASES - Abstract
Background: Cervical cancer is one of the most common gynecological malignancies. Previous studies have shown that the ethanol extract of Sophora moorcroftiana seeds (EESMS) possesses an antiproliferative effect on several tumors in vitro. Therefore, in this study, we assessed the impact of EESMS on human cervical carcinoma (HeLa) cell proliferation. Methods: The proliferation and apoptotic effects of HeLa cells treated with EESMS were evaluated using 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide assay, dual acridine orange/ethidium bromide double staining, flow cytometry, and western blotting. Single-cell level atomic force microscopy (AFM) was conducted to detect the mechanical properties of HeLa cells, and proteomics and bioinformatics methods were used to elucidate the molecular mechanisms of EESMS. Results: EESMS treatment inhibited HeLa cell proliferation by blocking the G0/G1 phase, increasing the expression of Caspase-3 and affecting its mechanical properties, and the EESMS indicated no significant inhibitory effect on mouse fibroblasts L929 cell line. In total, 218 differentially expressed proteins were identified using two-dimensional electrophoresis, and eight differentially expressed proteins were successfully identified using matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry. The differentially expressed proteins were involved in various cellular and biological processes. Conclusion: This study provides a perspective on how cells change through biomechanics and a further theoretical foundation for the future application of Sophora moorcroftiana as a novel low-toxicity chemotherapy medication for treating human cervical cancer. [ABSTRACT FROM AUTHOR]
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- 2024
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29. Fluoride impairs vascular smooth muscle A7R5 cell lines via disrupting amino acids metabolism.
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Li, Yan-Shu, Yang, Ru-Ru, Li, Xin-Ying, Liu, Wei-Wei, Zhao, Yi-Ming, Zu, Ming-Man, Gao, Yi-Hong, Huo, Min-Qi, Jiang, Yu-Ting, and Li, Bing-Yun
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AMINO acid metabolism ,VASCULAR smooth muscle ,MUSCLE cells ,CELL migration inhibition ,CELL lines - Abstract
Given the insidious and high-fatality nature of cardiovascular diseases (CVDs), the emergence of fluoride as a newly identified risk factor demands serious consideration alongside traditional risk factors. While vascular smooth muscle cells (VSMCs) play a pivotal role in the progression of CVDs, the toxicological impact of fluoride on VSMCs remains largely uncharted. In this study, we constructed fluorosis model in SD rats and A7R5 aortic smooth muscle cell lines to confirm fluoride impaired VSMCs. Fluoride aggravated the pathological damage of rat aorta in vivo. Then A7R5 were exposed to fluoride with concentration ranging from 0 to 1200 μmol/L over a 24-h period, revealing a dose-dependent inhibition of cell proliferation and migration. The further metabolomic analysis showed alterations in metabolite profiles induced by fluoride exposure, notably decreasing organic acids and lipid molecules level. Additionally, gene network analysis underscored the frequency of fluoride's interference with amino acids metabolism, potentially impacting the tricarboxylic acid (TCA) cycle. Our results also highlighted the ATP-binding cassette (ABC) transporters pathway as a central element in VSMC impairment. Moreover, we observed a dose-dependent increase in osteopontin (OPN) and α-smooth muscle actin (α-SMA) mRNA level and a dose-dependent decrease in ABC subfamily C member 1 (ABCC1) and bestrophin 1 (BEST1) mRNA level. These findings advance our understanding of fluoride as a CVD risk factor and its influence on VSMCs and metabolic pathways, warranting further investigation into this emerging risk factor. [ABSTRACT FROM AUTHOR]
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- 2024
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30. Proteomic characterization and cytotoxic potential of proteins from Cuscuta (Cuscuta epithymum (L.) crude herbal product against MCF-7 human breast cancer cell line.
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Akhtar, Umaima, Khurshid, Yamna, El-Aarag, Bishoy, Syed, Basir, Khan, Ishtiaq A., Parang, Keykavous, and Ahmed, Aftab
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PLANT protein analysis ,ADENOCARCINOMA ,IN vitro studies ,SUPEROXIDE dismutase ,COLORIMETRY ,LIQUID chromatography-mass spectrometry ,DATA analysis ,BREAST tumors ,APOPTOSIS ,CELL proliferation ,CELL lines ,BIOINFORMATICS ,MEDICINAL plants ,PROTEOMICS ,WESTERN immunoblotting ,ONE-way analysis of variance ,STATISTICS ,ANALYTICAL chemistry techniques ,CELL survival ,DATA analysis software ,PLANT proteins - Abstract
Background: The burden of breast cancer, the second leading cause of death worldwide, is increasing at an alarming rate. Cuscuta, used in traditional medicine for different ailments, including cancer, is known for containing phytochemicals that exhibit anticancer activity; however, the bioactivities of proteins from this plant remain unexplored. This study aimed to screen the cytotoxic potential of proteins from the crude herbal product of Cuscuta epithymum(L.) (CE) harvested from the host plants Alhagi maurorum and Medicago sativa. Methods: The proteins from CE were extracted using a salting-out method, followed by fractionation with a gel filtration chromatography column. Gel-free shotgun proteomics was subsequently performed for protein characterization. The viability assay using MTT was applied to deduce the cytotoxic potential of proteins against MCF-7 breast cancer cells, with further exploration of the effect of treatment on the expression of the apoptotic mediator BCL2-associated X protein (BAX) and B-cell lymphoma protein 2 (BCL-2) proteins, using western blotting to strengthen the findings from the in vitro viability assay. Results: The crude proteins (CP) of CE were separated into four protein peaks (P1, P2, P3, and P4) by gel filtration chromatography. The evaluation of potency showed a dose-dependent decline in the MCF-7 cell line after CP, P1, P2, and P3 treatment with the respective IC
50 values of 33.8, 43.1, 34.5, and 28.6 µg/ml. The percent viability of the cells decreased significantly upon treatment with 50 µg/ml CP, P1, P2, and P3 (P < 0.001). Western-blot analysis revealed upregulation of proapoptotic protein BAX in the cells treated with CP, P3 (P < 0.01), and P2 (P < 0.05); however, the antiapoptotic protein, BCL-2 was downregulated in the cells treated with CP and P3 (P < 0.01), but no significant change was detected in P2 treated cells. The observed cytotoxic effects of proteins in the CP, P1, P2, and P3 from the in vitro viability assay and western blot depicted the bioactivity potential of CE proteins. The database search revealed the identities of functionally important proteins, including nonspecific lipid transfer protein, superoxide dismutase, carboxypeptidase, RNase H domain containing protein, and polyribonucleotide nucleotidyltransferase, which have been previously reported from other plants to exhibit anticancer activity. Conclusion: This study indicated the cytotoxic activity of Cuscuta proteins against breast cancer MCF-7 cells and will be utilized for future investigations on the mechanistic effect of active proteins. The survey of CE proteins provided substantial data to encourage further exploration of biological activities exhibited by proteins in Cuscuta. [ABSTRACT FROM AUTHOR]- Published
- 2024
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31. Establishment and partial characterisation of a new cell line derived from adult tissues of the tsetse fly Glossina morsitans morsitans.
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Bell-Sakyi, Lesley, Haines, Lee R., Petrucci, Giovanni, Beliavskaia, Alexandra, Hartley, Catherine, Khoo, Jing Jing, Makepeace, Benjamin L., Abd-Alla, Adly M. M., and Darby, Alistair C.
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TSETSE-flies ,CELL lines ,CYTOMEGALOVIRUSES ,BIOLOGICAL evolution ,SALIVARY glands ,DISEASE vectors - Abstract
Background: Insect cell lines play a vital role in many aspects of research on disease vectors and agricultural pests. The tsetse fly Glossina morsitans morsitans is an important vector of salivarian trypanosomes in sub-Saharan Africa and, as such, is a major constraint on human health and agricultural development in the region. Methods: Here, we report establishment and partial characterisation of a cell line, GMA/LULS61, derived from tissues of adult female G. m. morsitans. GMA/LULS61 cells, grown at 28 °C in L-15 (Leibovitz) medium supplemented with foetal bovine serum and tryptose phosphate broth, have been taken through 23 passages to date and can be split 1:1 at 2-week intervals. Karyotyping at passage 17 revealed a predominantly haploid chromosome complement. Species origin and absence of contaminating bacteria were confirmed by PCR amplification and sequencing of fragments of the COI gene and pan-bacterial 16S rRNA gene respectively. However, PCR screening of RNA extracted from GMA/LULS61 cells confirmed presence of the recently described Glossina morsitans morsitans iflavirus and Glossina morsitans morsitans negevirus, but absence of Glossina pallipides salivary gland hypertrophy virus. GMA/LULS61 cells supported infection and growth of 6/7 different insect-derived strains of the intracellular bacterial symbiont Wolbachia. Conclusions: The GMA/LULS61 cell line has potential for application in a variety of studies investigating the biology of G. m. morsitans and its associated pathogenic and symbiotic microorganisms. [ABSTRACT FROM AUTHOR]
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- 2024
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32. Comprehensive analysis of the REST transcription factor regulatory networks in IDH mutant and IDH wild-type glioma cell lines and tumors.
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Perycz, Malgorzata, Dabrowski, Michal J., Jardanowska-Kotuniak, Marta, Roura, Adria-Jaume, Gielniewski, Bartlomiej, Stepniak, Karolina, Dramiński, Michał, Ciechomska, Iwona A., Kaminska, Bozena, and Wojtas, Bartosz
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TRANSCRIPTION factors ,EPIGENOMICS ,GENE regulatory networks ,GLIOMAS ,CELL lines ,GENE expression - Abstract
The RE1-silencing transcription factor (REST) acts either as a repressor or activator of transcription depending on the genomic and cellular context. REST is a key player in brain cell differentiation by inducing chromatin modifications, including DNA methylation, in a proximity of its binding sites. Its dysfunction may contribute to oncogenesis. Mutations in IDH1/2 significantly change the epigenome contributing to blockade of cell differentiation and glioma development. We aimed at defining how REST modulates gene activation and repression in the context of the IDH mutation-related phenotype in gliomas. We studied the effects of REST knockdown, genome wide occurrence of REST binding sites, and DNA methylation of REST motifs in IDH wild type and IDH mutant gliomas. We found that REST target genes, REST binding patterns, and TF motif occurrence proximal to REST binding sites differed in IDH wild-type and mutant gliomas. Among differentially expressed REST targets were genes involved in glial cell differentiation and extracellular matrix organization, some of which were differentially methylated at promoters or gene bodies. REST knockdown differently impacted invasion of the parental or IDH1 mutant glioma cells. The canonical REST-repressed gene targets showed significant correlation with the GBM NPC-like cellular state. Interestingly, results of REST or KAISO silencing suggested the interplay between these TFs in regulation of REST-activated and repressed targets. The identified gene regulatory networks and putative REST cooperativity with other TFs, such as KAISO, show distinct REST target regulatory networks in IDH-WT and IDH-MUT gliomas, without concomitant DNA methylation changes. We conclude that REST could be an important therapeutic target in gliomas. [ABSTRACT FROM AUTHOR]
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- 2024
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33. Hindering the biofilm of microbial pathogens and cancer cell lines development using silver nanoparticles synthesized by epidermal mucus proteins from Clarias gariepinus.
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Alabssawy, Ahmed N., Abu-Elghait, Mohammed, Azab, Ahmad M., Khalaf-Allah, Hassan M. M., Ashry, Abdelrahman S., Ali, Ahmed O. M., Sabra, Abu-Bakr A. A., and Salem, Salem S.
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CLARIAS gariepinus ,SILVER nanoparticles ,CELL lines ,CANCER cells ,MUCUS ,QUORUM sensing - Abstract
Scientists know very little about the mechanisms underlying fish skin mucus, despite the fact that it is a component of the immune system. Fish skin mucus is an important component of defence against invasive infections. Recently, Fish skin and its mucus are gaining interest among immunologists. Characterization was done on the obtained silver nanoparticles Ag combined with Clarias gariepinus catfish epidermal mucus proteins (EMP-Ag-NPs) through UV–vis, FTIR, XRD, TEM, and SEM. Ag-NPs ranged in size from 4 to 20 nm, spherical in form and the angles were 38.10°, 44.20°, 64.40°, and 77.20°, Where wavelength change after formation of EMP-Ag-NPs as indicate of dark brown, the broad band recorded at wavelength at 391 nm. Additionally, the antimicrobial, antibiofilm and anticancer activities of EMP-Ag-NPs was assessed. The present results demonstrate high activity against unicellular fungi C. albicans, followed by E. faecalis. Antibiofilm results showed strong activity against both S. aureus and P. aeruginosa pathogens in a dose-dependent manner, without affecting planktonic cell growth. Also, cytotoxicity effect was investigated against normal cells (Vero), breast cancer cells (Mcf7) and hepatic carcinoma (HepG2) cell lines at concentrations (200–6.25 µg/mL) and current results showed highly anticancer effect of Ag-NPs at concentrations 100, 5 and 25 µg/mL exhibited rounding, shrinkage, deformation and granulation of Mcf7 and HepG2 with IC50 19.34 and 31.16 µg/mL respectively while Vero cells appeared rounded at concentration 50 µg/mL and normal shape at concentration 25, 12.5 and 6.25 µg/ml with IC50 35.85 µg/mL. This study evidence the potential efficacy of biologically generated Ag-NPs as a substitute medicinal agent against harmful microorganisms. Furthermore, it highlights their inhibitory effect on cancer cell lines. [ABSTRACT FROM AUTHOR]
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- 2024
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34. Anticancer properties and metabolomic profiling of Shorea roxburghii extracts toward gastrointestinal cancer cell lines.
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Janthamala, Sutthiwan, Promraksa, Bundit, Thanee, Malinee, Duenngai, Kunyarat, Jusakul, Apinya, Kongpetch, Sarinya, Kraiklang, Ratthaphol, Thanee, Kidsada, Pinlaor, Porntip, Namwat, Nisana, Saya, Hideyuki, and Techasen, Anchalee
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GASTROINTESTINAL tumors ,FLOW cytometry ,RESEARCH funding ,ANTINEOPLASTIC agents ,FLAVONOIDS ,APOPTOSIS ,PHYTOCHEMICALS ,PLANT extracts ,CELL lines ,REACTIVE oxygen species ,MEDICINAL plants ,ANTIOXIDANTS ,PHENOLS ,METABOLOMICS ,CELL survival ,PHARMACODYNAMICS - Abstract
Background: Gastrointestinal cancer (GIC) ranks as the highest cause of cancer-related deaths globally. GIC patients are often diagnosed at advanced stages, limiting effective treatment options. Chemotherapy, the common GIC recommendation, has significant disadvantages such as toxicity and adverse effects. Natural products contain substances with diverse pharmacological characteristics that promise for use in cancer therapeutics. In this study, the flower of renowned Asian medicinal plant, Shorea roxburghii was collected and extracted to investigate its phytochemical contents, antioxidant, and anticancer properties on GIC cells. Methods: The phytochemical contents of Shorea roxburghii extract were assessed using suitable methods. Phenolic content was determined through the Folin-Ciocalteu method, while flavonoids were quantified using the aluminum chloride (AlCl
3 ) method. Antioxidant activity was evaluated using the FRAP and DPPH assays. Cytotoxicity was assessed in GIC cell lines via the MTT assay. Additionally, intracellular ROS levels and apoptosis were examined through flow cytometry techniques. The correlation between GIC cell viability and phytochemicals,1 H-NMR analysis was conducted. Results: Among the four different solvent extracts, ethyl acetate extract had the highest phenolic and flavonoid contents. Water extract exhibited the strongest reducing power and DPPH scavenging activity following by ethyl acetate. Interestingly, ethyl acetate extract demonstrated the highest inhibitory activity against three GIC cell lines (KKU-213B, HepG2, AGS) with IC50 values of 91.60 µg/ml, 39.38 µg/ml, and 35.59 µg/ml, while showing less toxicity to normal fibroblast cells. Ethyl acetate extract induced reactive oxygen species and apoptosis in GIC cell lines by downregulating anti-apoptotic protein Bcl-2. Metabolic profiling-based screening revealed a positive association between reduced GIC cell viability and phytochemicals like cinnamic acid and its derivatives, ferulic acid and coumaric acid. Conclusions: This study highlights the potential of natural compounds in Shorea roxburghii in the development of more effective and safer anticancer agents as options for GIC as well as shedding light on new avenues for cancer treatment. [ABSTRACT FROM AUTHOR]- Published
- 2024
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35. Ginsenoside compound K induces ferroptosis via the FOXO pathway in liver cancer cells.
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Chen, Jiaxin, Wang, Zhuoshi, Fu, Jinghao, Cai, Yuesong, Cheng, Haoyi, Cui, Xinmu, Sun, Manqing, Liu, Mingyue, and Zhang, Xuewu
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LIVER tumors ,CHINESE medicine ,RESEARCH funding ,PHOSPHORYLATION ,T-test (Statistics) ,CELL proliferation ,PHARMACEUTICAL chemistry ,CELLULAR signal transduction ,ULTRASONIC imaging ,DESCRIPTIVE statistics ,CELL lines ,MICE ,GENE expression ,IMMUNOHISTOCHEMISTRY ,CELL death ,ANIMAL experimentation ,MOLECULAR structure ,SPECTRUM analysis ,WESTERN immunoblotting ,ONE-way analysis of variance ,GINSENG ,BIOLOGICAL assay ,COMPARATIVE studies ,DATA analysis software ,CELL survival - Abstract
Liver cancer is a common malignant tumor worldwide, traditional Chinese medicine is one of the treatment measures for liver cancer because of its good anti-tumor effects and fewer toxic side effects. Ginsenoside CK (CK) is an active component of ginseng. This study explored the mechanism by which CK induced ferroptosis in liver cancer cells. We found that CK inhibited the proliferation of HepG2 and SK-Hep-1 cells, induced ferroptosis of cells. Ferrostatin-1, an ferroptosis inhibitor, was used to verify the role of CK in inducing ferroptosis of liver cancer cells. Network pharmacological analysis identified the FOXO pathway as a potential mechanism of CK, and western blot showed that CK inhibited p-FOXO1. In cells treated with the FOXO1 inhibitor AS1842856, further verify the involvement of the FOXO pathway in regulating CK-induced ferroptosis in HepG2 and SK-Hep-1 cells. A HepG2 cell–transplanted tumor model was established in nude mice, and CK inhibited the growth of transplanted tumors in nude mice, p-FOXO1 was decreased in tumor tissues, and SLC7A11 and GPX4 expressions were also down-regulated after CK treatment. These findings suggested that CK induces ferroptosis in liver cancer cells by inhibiting FOXO1 phosphorylation and activating the FOXO signaling pathway, thus playing an antitumor role. [ABSTRACT FROM AUTHOR]
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- 2024
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36. Systematic optimization and evaluation of culture conditions for the construction of circulating tumor cell clusters using breast cancer cell lines.
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Zou, Jueyao, Chen, Qiong, He, Yong, Pan, Yanhong, Zhao, Han, Shi, Junfeng, Wei, Zhonghong, Yu, Suyun, Zhao, Yang, Han, Xin, Lu, Yin, and Chen, Wenxing
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BREAST cancer ,CELL lines ,CANCER cells ,METASTASIS ,TRANSMISSION electron microscopy - Abstract
Background: Circulating tumor cell (CTC) clusters play a critical role in carcinoma metastasis. However, the rarity of CTC clusters and the limitations of capture techniques have retarded the research progress. In vitro CTC clusters model can help to further understand the biological properties of CTC clusters and their clinical significance. Therefore, it is necessary to establish reliable in vitro methodological models to form CTC clusters whose biological characteristics are very similar to clinical CTC clusters. Methods: The assays of immunofluorescence, transmission electron microscopy, EdU incorporation, cell adhension and microfluidic chips were used. The experimental metastasis model in mice was used. Results: We systematically optimized the culture methods to form in vitro CTC clusters model, and more importantly, evaluated it with reference to the biological capabilities of reported clinical CTC clusters. In vitro CTC clusters exhibited a high degree of similarity to the reported pathological characteristics of CTC clusters isolated from patients at different stages of tumor metastasis, including the appearance morphology, size, adhesive and tight junctions-associated proteins, and other indicators of CTC clusters. Furthermore, in vivo experiments also demonstrated that the CTC clusters had an enhanced ability to grow and metastasize compared to single CTC. Conclusions: The study provides a reliable model to help to obtain comparatively stable and qualified CTC clusters in vitro, propelling the studies on tumor metastasis. [ABSTRACT FROM AUTHOR]
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- 2024
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37. scGAL: unmask tumor clonal substructure by jointly analyzing independent single-cell copy number and scRNA-seq data.
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Li, Ruixiang, Shi, Fangyuan, Song, Lijuan, and Yu, Zhenhua
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GENERATIVE adversarial networks ,GENE amplification ,GENE expression ,GENE expression profiling ,DNA sequencing ,CELL lines - Abstract
Background: Accurately deciphering clonal copy number substructure can provide insights into the evolutionary mechanism of cancer, and clustering single-cell copy number profiles has become an effective means to unmask intra-tumor heterogeneity (ITH). However, copy numbers inferred from single-cell DNA sequencing (scDNA-seq) data are error-prone due to technically confounding factors such as amplification bias and allele-dropout, and this makes it difficult to precisely identify the ITH. Results: We introduce a hybrid model called scGAL to infer clonal copy number substructure. It combines an autoencoder with a generative adversarial network to jointly analyze independent single-cell copy number profiles and gene expression data from same cell line. Under an adversarial learning framework, scGAL exploits complementary information from gene expression data to relieve the effects of noise in copy number data, and learns latent representations of scDNA-seq cells for accurate inference of the ITH. Evaluation results on three real cancer datasets suggest scGAL is able to accurately infer clonal architecture and surpasses other similar methods. In addition, assessment of scGAL on various simulated datasets demonstrates its high robustness against the changes of data size and distribution. scGAL can be accessed at: https://github.com/zhyu-lab/scgal. Conclusions: Joint analysis of independent single-cell copy number and gene expression data from a same cell line can effectively exploit complementary information from individual omics, and thus gives more refined indication of clonal copy number substructure. [ABSTRACT FROM AUTHOR]
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- 2024
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38. Study on the differential hepatotoxicity of raw polygonum multiflorum and polygonum multiflorum praeparata and its mechanism.
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Huang, Chaowen, Jiang, Yu, Bao, Qing, Wang, Lu, Tang, Lin, Liu, Yanjuan, and Yang, Lei
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CHINESE medicine ,FLOW cytometry ,HEPATOTOXICOLOGY ,RADIOIMMUNOASSAY ,T-test (Statistics) ,RESEARCH funding ,HERBAL medicine ,BLOOD collection ,ASPARTATE aminotransferase ,CELL proliferation ,BILIRUBIN ,DESCRIPTIVE statistics ,MICE ,GENE expression ,REACTIVE oxygen species ,SERUM ,CELL lines ,ANIMAL experimentation ,WESTERN immunoblotting ,CELL death ,ALANINE aminotransferase ,ANALYSIS of variance ,STAINS & staining (Microscopy) ,CELL survival ,DATA analysis software ,BIOMARKERS ,SEQUENCE analysis ,LIVER function tests - Abstract
Background: Polygonum multiflorum (PM), a widely used traditional Chinese medicine herb, is divided into two forms, namely raw polygonum multiflorum (RPM) and polygonum multiflorum praeparata (PMP), according to the processing procedure. Emerging data has revealed the differential hepatotoxicity of RPM and PMP, however, its potential mechanism is still unclear. Methods: In our study, we investigated the differential hepatotoxicity of RPM and PMP exerted in C57BL/6 mice. First, sera were collected for biochemical analysis and HE staining was applied to examine the morphological alternation of the liver. Then we treated L02 cells with 5 mg / mL of RPM or PMP. The CCK8 and EdU assays were utilized to observe the viability and proliferation of L02 cells. RNA sequencing was performed to explore the expression profile of L02 cells. Western blotting was performed to detect the expression level of ferroptosis-related protein. Flow cytometry was used to evaluate ROS accumulation. Results: In our study, a significant elevation in serum ALT, AST and TBIL levels was investigated in the RMP group, while no significant differences were observed in the PMP group, compared to that of the CON group. HE staining showed punctate necrosis, inflammatory cell infiltration and structural destruction can be observed in the RPM group, which can be significantly attenuated after processing. In addition, we also found RPM could decrease the viability and proliferation capacity of L02 cells, which can be reversed by ferroptosis inhibitor. RNA sequencing data revealed the adverse effect of PM exerted on the liver is closely associated with ferroptosis. Western blotting assay uncovered the protein level of GPX4, HO-1 and FTL was sharply decreased, while the ROS content was dramatically elevated in L02 cells treated with RPM, which can be partially restored after processing. Conclusions: The hepatotoxicity induced by RPM was significantly lower than the PMP, and its potential mechanism is associated with ferroptosis. [ABSTRACT FROM AUTHOR]
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- 2024
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39. An anthocyanin-rich extract from Zea mays L. var. ceratina alleviates neuronal cell death caused by hydrogen peroxide-induced cytotoxicity in SH-SY5Y cells.
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Mairuae, Nootchanat, Palachai, Nut, and Noisa, Parinya
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SYNDROMES ,NEUROPROTECTIVE agents ,SUPEROXIDE dismutase ,NEUROTOXICOLOGY ,RESEARCH funding ,NEURONS ,APOPTOSIS ,OXIDATIVE stress ,DESCRIPTIVE statistics ,PLANT extracts ,CELL lines ,REACTIVE oxygen species ,HYDROGEN peroxide ,CELL death ,ANTIOXIDANTS ,BIOLOGICAL pigments ,CELL survival ,TRANSFERASES ,DEMENTIA ,DATA analysis software ,NEUROBLASTOMA ,CASPASES - Abstract
The incidence of dementia is rising, with neuronal cell death from oxidative stress and apoptosis recognized as a significant contributor to its development. However, effective strategies to combat this condition are lacking, necessitating further investigation. This study aimed to assess the potential of an anthocyanin-rich extract from Zea mays L. var. ceratina (AZC) in alleviating neuronal cell death. Neurotoxicity was induced in SH-SY5Y cells using hydrogen peroxide (H
2 O2 ) at a concentration of 200 µM. Cells were pretreated with varying doses (31.25 and 62.5 µg/mL) of AZC. Cell viability was assessed using the MTT assay, and molecular mechanisms including reactive oxygen species (ROS) levels, antioxidant enzyme activities (catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px)), malondialdehyde (MDA) levels for oxidative stress, and the activation of extracellular signal-regulated kinases 1 and 2 (ERK1/2), cAMP response element-binding protein (CREB), and apoptotic factors (B-cell lymphoma 2 (Bcl-2), caspase 3) were explored. Results showed that AZC significantly improved cell viability, reduced ROS production and MDA levels, and downregulated caspase 3 expression. It enhanced CAT, SOD, and GSH-Px activities, activated ERK1/2 and CREB, and upregulated Bcl-2 expression. These findings support the neuroprotective effects of AZC, suggesting it activates ERK1/2, leading to CREB activation and subsequent upregulation of Bcl-2 expression while suppressing caspase 3. AZC may mitigate neuronal cell death by reducing ROS levels through enhanced scavenging enzyme activities. In conclusion, this study underscores the potential of AZC as a neuroprotective agent against neuronal cell death. However, further investigations including toxicity assessments, in vivo studies, and clinical trials are necessary to validate its benefits in neuroprotection. [ABSTRACT FROM AUTHOR]- Published
- 2024
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40. The metabolic reprogramming of γ-aminobutyrate in oral squamous cell carcinoma.
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Wu, Shi-Lian, Zha, Guang-Yu, Tian, Ke-Bin, Xu, Jun, and Cao, Ming-Guo
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HEAD & neck cancer diagnosis ,RNA analysis ,GLUTAMINE metabolism ,GLUTAMIC acid metabolism ,SQUAMOUS cell carcinoma ,AMIDASES ,MOUTH tumors ,NUCLEAR magnetic resonance spectroscopy ,MITOCHONDRIA ,RESEARCH funding ,HEAD & neck cancer ,POLYMERASE chain reaction ,CANCER patients ,LYASES ,DESCRIPTIVE statistics ,METABOLIC reprogramming ,CELL lines ,GENE expression ,WESTERN immunoblotting ,METABOLOMICS ,GABA ,SEQUENCE analysis - Abstract
Oral squamous cell carcinoma (OSCC) is the most common head and neck malignancy. The oncometabolites have been studied in OSCC, but the mechanism of metabolic reprogramming remains unclear. To identify the potential metabolic markers to distinguish malignant oral squamous cell carcinoma (OSCC) tissue from adjacent healthy tissue and study the mechanism of metabolic reprogramming in OSCC. We compared the metabolites between cancerous and paracancerous tissues of OSCC patients by
1 HNMR analysis. We established OSCC derived cell lines and analyzed their difference of RNA expression by RNA sequencing. We investigated the metabolism of γ-aminobutyrate in OSCC derived cells by real time PCR and western blotting. Our data revealed that much more γ-aminobutyrate was produced in cancerous tissues of OSCC patients. The investigation based on OSCC derived cells showed that the increase of γ-aminobutyrate was promoted by the synthesis of glutamate beyond the mitochondria. In OSCC cancerous tissue derived cells, the glutamate was catalyzed to glutamine by glutamine synthetase (GLUL), and then the generated glutamine was metabolized to glutamate by glutaminase (GLS). Finally, the glutamate produced by glutamate-glutamine-glutamate cycle was converted to γ-aminobutyrate by glutamate decarboxylase 2 (GAD2). Our study is not only benefit for understanding the pathological mechanisms of OSCC, but also has application prospects for the diagnosis of OSCC. [ABSTRACT FROM AUTHOR]- Published
- 2024
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41. Phytochemical analysis and evaluation of its antioxidant, antimicrobial, and cytotoxic activities for different extracts of Casuarina equisetifolia.
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Abdallah, Walid Elsayed, Shams, Khaled Ahmed, and El-Shamy, Ashraf Moursi
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AUTOPHAGY ,RESEARCH funding ,HYDROCARBONS ,PHYTOCHEMICALS ,DESCRIPTIVE statistics ,CYTOTOXINS ,ANTI-infective agents ,PLANT extracts ,CELL lines ,ANTIOXIDANTS ,MOLECULAR structure ,ONE-way analysis of variance ,CELL death ,DATA analysis software ,PHARMACODYNAMICS - Abstract
Background: Casuarina equisetifolia belongs to the Casuarina species with the most extensive natural distribution, which contain various phytochemicals with potential health benefits. This study aimed to investigate the chemical composition and biological activities of different extracts of Casuarina equisetifolia. Methods: The n-hexane extract was analyzed for its unsaponifiable and fatty acid methyl esters fractions, while chloroform, ethyl acetate, and butanol extracts were studied for their phenolic components. Six different extracts of C. equisetifolia needles were evaluated for their total phenolic content, total flavonoid content, and their antioxidant, antimicrobial, and cytotoxic activities. Results: The n-hexane extract contained mainly hydrocarbons and fatty acid methyl esters, while ten phenolic compounds were isolated and identified in the chloroform, ethyl acetate, and butanol extracts. The methanolic extract exhibited the highest total phenolic and flavonoid content, highest antioxidant activity, and most potent cytotoxic activity against HepG-2 and HCT-116 cancer cell lines. The ethyl acetate extract showed the most significant inhibition zone against Staphylococcus aureus and Bacillus subtilis. Conclusion: Casuarina equisetifolia extracts showed promising antioxidant, antimicrobial, and cytotoxic activities. Overall, Casuarina equisetifolia is a versatile tree with a variety of uses, and its plant material can be used for many different purposes. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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42. Phytoconstituent analysis, anti-inflammatory, antimicrobial and anticancer effects of nano encapsulated Convolvulus arvensis L. extracts.
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Osman, Ezzat E. A., Shemis, Mohamed A., Abdel-Hameed, El-Sayed S., Gouda, Abdullah E., Hassan, Hanem, Atef, Nahla, and Mamdouh, Samah
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ANTIBIOTICS assay ,ANTI-inflammatory agents ,ALGINATES ,LIQUID chromatography-mass spectrometry ,ANTINEOPLASTIC agents ,CHEMICAL processes ,FLAVONOIDS ,HYDROCARBONS ,LIPIDS ,DESCRIPTIVE statistics ,PLANT extracts ,CELL lines ,POLYSACCHARIDES ,ESCHERICHIA coli ,NANOTECHNOLOGY ,PHENOLS ,ALCOHOLS (Chemical class) ,NANOPARTICLES - Abstract
Background: The Convolvulus genus is distributed all over the world and has a long history in traditional medicine. As nanotechnology expands its reach into areas like drug delivery and biomedicine, this study intends to assess the potential of Convolvulus arvensis L. extracts as anti-bacterial, anti-inflammatory and anti-cancer agents, along with chemical profiling of the methanolic (MeOH) extract active ingredients. Methods: The chemical composition of an 85% MeOH extract was investigated by liquid chromatography with an electrospray source connected to mass spectrometry (LC-ESI-MS). Both the 85% MeOH extract and n-butanol fraction of C. arvensis were loaded for the first time on alginate/chitosan nanoparticles. The 85% MeOH extract, n-butanol fraction and their loaded nanoparticles were tested for their cytotoxicity, anticancer, anti-inflammatory and antibacterial activity (against pathogenic bacteria, E. coli and S. aureus). Results: The chemical investigation of 85% MeOH extract of C. arvensis underwent LC-ESI-MS analysis, revealing twenty-six phenolic substances, of which 16 were phenolic acids, 6 were flavonoids, 1 glycolipid, 1 sesquiterpene and 2 unknown compounds. The FT-IR spectra confirmed the encapsulation of the 85% MeOH extract and n-butanol fraction onto alginate/chitosan nanoparticles and small size obtained by TEM maintained them nontoxic and enhanced their anti-inflammatory activity (the IC
50 was decreased from 1050 to 175 µg/ml). The anti-cancer activity against HepG2 was increased and the cell viability was decreased from 28.59 ± 0.52 to 20.80 ± 0.27 at a maximum concentration of 1000 µg/ml. In addition, the MIC of encapsulated extracts was decreased from 31.25 to7.78 µg/ml in E. coli (Gm-ve) and from 15.56 to 7.78 µg/ml in S. aureus (Gm + ve) bacteria. Conclusion: Both alginate and chitosan are excellent natural polymers for the encapsulation process, which affects positively on the bioactive constituents of C. arvensis extracts and improves their biological properties. [ABSTRACT FROM AUTHOR]- Published
- 2024
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43. PPARG activation promotes the proliferation of colorectal cancer cell lines and enhances the antiproliferative effect of 5-fluorouracil.
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Schöckel, Leah, Woischke, Christine, Surendran, Sai Agash, Michl, Marlies, Schiergens, Tobias, Hölscher, Andreas, Glass, Florian, Kreissl, Peter, Klauschen, Frederick, Günther, Michael, Ormanns, Steffen, and Neumann, Jens
- Subjects
CANCER cell proliferation ,CELL lines ,TYPE 2 diabetes ,PEROXISOME proliferator-activated receptors ,NUCLEAR receptors (Biochemistry) ,FLUOROURACIL - Abstract
Background: Peroxisome proliferator-activated receptor gamma (PPARG) is a member of the nuclear receptor family. It is involved in the regulation of adipogenesis, lipid metabolism, insulin sensitivity, vascular homeostasis and inflammation. In addition, PPARG agonists, known as thiazolidinediones, are well established in the treatment of type 2 diabetes mellitus. PPARGs role in cancer is a matter of debate, as pro- and anti-tumour properties have been described in various tumour entities. Currently, the specific role of PPARG in patients with colorectal cancer (CRC) is not fully understood. Material and methods: The prognostic impact of PPARG expression was investigated by immunohistochemistry in a case-control study using a matched pair selection of CRC tumours (n = 246) with either distant metastases to the liver (n = 82), lung (n = 82) or without distant metastases (n = 82). Its effect on proliferation as well as the sensitivity to the chemotherapeutic drug 5-fluorouracil (5-FU) was examined after activation, inhibition, and transient gene knockdown of PPARG in the CRC cell lines SW403 and HT29. Results: High PPARG expression was significantly associated with pulmonary metastasis (p = 0.019). Patients without distant metastases had a significantly longer overall survival with low PPARG expression in their tumours compared to patients with high PPARG expression (p = 0.045). In the pulmonary metastasis cohort instead, a trend towards longer survival was observed for patients with high PPARG expression in their tumour (p = 0.059). Activation of PPARG by pioglitazone and rosiglitazone resulted in a significant dose-dependent increase in proliferation of CRC cell lines. Inhibition of PPARG by its specific inhibitor GW9662 and siRNA-mediated knockdown of PPARG significantly decreased proliferation. Activating PPARG significantly increased the CRC cell lines sensitivity to 5-FU while its inhibition decreased it. Conclusion: The prognostic effect of PPARG expression depends on the metastasis localization in advanced CRC patients. Activation of PPARG increased malignancy associated traits such as proliferation in CRC cell lines but also increases sensitivity towards the chemotherapeutic agent 5-FU. Based on this finding, a combination therapy of PPARG agonists and 5-FU-based chemotherapy constitutes a promising strategy which should be further investigated. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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44. Chili pepper extracts, capsaicin, and dihydrocapsaicin as potential anticancer agents targeting topoisomerases.
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Hudáková, Terézia, Šemeláková, Martina, Očenáš, Peter, Kožurková, Mária, Krochtová, Kristína, Sovová, Simona, Tóthová, Zuzana, Guľášová, Zuzana, Popelka, Peter, and Solár, Peter
- Subjects
COLON tumors ,PILOT projects ,IN vitro studies ,HIGH performance liquid chromatography ,ONE-way analysis of variance ,ANTINEOPLASTIC agents ,CELL proliferation ,DESCRIPTIVE statistics ,TOXICITY testing ,PLANT extracts ,DNA damage ,CELL lines ,DATA analysis software ,CAPSAICIN ,HOT peppers ,ENZYME inhibitors ,PHARMACODYNAMICS - Abstract
DNA topoisomerases regulate conformational changes in DNA topology during normal cell growth, such as replication, transcription, recombination, and repair, and may be targeted for anticancer drugs. A DNA topology assay was used to investigate DNA-damaging/protective activities of extracts from Habanero Red (HR), Habanero Maya Red (HMR), Trinidad Moruga Scorpion (TMS), Jalapeno (J), Serrano pepper (SP), Habanero Red Savina (HRS), Bhut Jolokia (BJ), and Jamaica Rosso (JR) peppers, demonstrating their inhibitory effect on the relaxation of pBR by Topo I. DNA topoisomerase II (Topo II) is proven therapeutic target of anticancer drugs. Complete inhibition of Topo II was observed for samples TMS, HR, and HMR. Extracts J and SP had the lowest capsaicin and dihydrocapsaicin content compared to other peppers. HR, HMR, TMS, J, S, HRS, BJ, JR extracts showed the anticancer effect, examined by MTS and xCell assay on the in vitro culture of human colon carcinoma cell line HCT116. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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45. Chemical composition, anticancer, antimicrobial activity of Aloysia citriodora Palau essential oils from four different locations in Palestine.
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Al-Maharik, Nawaf, Salama, Yousef, Al-Hajj, Nisreen, Jaradat, Nidal, Jobran, Naji Thaer, Warad, Ismael, Hamdan, Lina, Alrob, Moataz Abo, Sawafta, Asil, and Hidmi, Adel
- Subjects
T-test (Statistics) ,DATA analysis ,ESSENTIAL oils ,ANTINEOPLASTIC agents ,DRUG resistance in microorganisms ,PHYTOCHEMICALS ,REVERSE transcriptase polymerase chain reaction ,DESCRIPTIVE statistics ,PLANT extracts ,ANTI-infective agents ,GAS chromatography ,CELL lines ,RNA ,CELL culture ,MEDICINAL plants ,MASS spectrometry ,RESEARCH methodology ,ANALYSIS of variance ,STATISTICS - Abstract
The primary aim of this investigation was to determine the anticancer and antimicrobial properties of essential oils (EOs) extracted from the leaves of Aloysia citriodora Palau, which were procured from four separate locations in Palestine, in addition to analyzing their chemical composition. These areas include Jericho, which has the distinction of being the lowest location on Earth, at 260 m below sea level. The EOs were acquired by hydrodistillation, and their chemical composition was examined utilizing gas chromatography-mass spectrometry (GC-MS). The minimum inhibitory concentration (MIC) of EOs was assessed against six bacterial strains and one fungal species using 96-well microtiter plates. The primary components found in these oils are geranial (26.32–37.22%), neral (18.38–29.00%), and α-curcumene (7.76–16.91%) in three regions. α-Curcumene (26.94%), spathulenol (13.69%), geranial (10.79%), caryophyllene oxide (8.66%), and neral (7.59%) were found to be the most common of the 32 chemical components in the EO from Jericho. The EOs exhibited bactericidal properties, particularly against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus (MRSA), and showed highly effective fungicidal activity. Nevertheless, the antifungal efficacy of the EO was found to surpass its antibacterial activity when administered at lower dosages. The EOs exhibited anticancer activities against melanoma cancer cells, as indicated by their IC
50 values, which ranged from 4.65 to 7.96 μg/mL. A. citriodora EO possesses substantial antifungal and anticancer characteristics, rendering it appropriate for utilization in food-related contexts, hence potentially enhancing the sustainability of the food sector. [ABSTRACT FROM AUTHOR]- Published
- 2024
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46. Tanreqing injection inhibits dengue virus encephalitis by suppressing the activation of NLRP3 inflammasome.
- Author
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Huang, Hefei, He, Xuemei, Shi, Lingzhu, Yu, Jingtao, Lu, Zibin, Cao, Huihui, Ou, Jinying, Chen, Xi, Yan, Lijun, Yang, Jiabin, Zhao, Wei, Liu, Junshan, and Yu, Linzhong
- Subjects
BRAIN physiology ,KIDNEY physiology ,ENCEPHALITIS viruses ,PROTEINS ,BIOLOGICAL models ,HAMSTERS ,INTERLEUKINS ,FLOW cytometry ,HERBAL medicine ,INJECTIONS ,DENGUE ,HIPPOCAMPUS (Brain) ,ANIMAL experimentation ,ANTI-inflammatory agents ,WESTERN immunoblotting ,SIGNAL peptides ,CELLS ,ENZYME-linked immunosorbent assay ,DESCRIPTIVE statistics ,RESEARCH funding ,CELL lines ,POLYMERASE chain reaction ,CHINESE medicine ,MICE ,CHEMICAL inhibitors ,THERAPEUTICS - Abstract
Background: Encephalitis caused by dengue virus (DENV) is considered a manifestation of severe dengue. Tanreqing injection (TRQ) is a well-known Chinese patented medicine, which has been used to treat brain-related disorders by inhibiting inflammation. Nevertheless, the effects of TRQ on DENV encephalitis have not been studied. The aim of this study was to evaluate the effects of TRQ on DENV encephalitis and to explore its potential mechanisms. Methods: The cytotoxicity of TRQ was examined by MTT assay, and the anti-DENV activities of TRQ in BHK-21 baby hamster kidney fibroblast were evaluated through CCK-8 and plaque assays. The expression levels of NO, IL1B/IL-1β, TNFα and IL6 were measured by qRT‒PCR and ELISA in the BV2 murine microglial cell line. The inhibitory effects of TRQ on NLRP3 inflammasome activation in BV2 cells were examined by Western blotting, qRT‒PCR and ELISA. The effects of TRQ on HT22 mouse hippocampal neuronal cells were examined by CCK-8 assay, morphology observation and flow cytometry. Moreover, a DENV-infected ICR suckling mouse model was developed to investigate the protective role of TRQ in vivo. Results: TRQ decreased the release of NO, IL6, TNFα and IL1B from BV2 cells and inhibited the activation of NLRP3. The presence of the NLRP3 agonist nigericin reversed the anti-inflammatory activities of TRQ. Furthermore, TRQ inhibited the death of HT22 cells by decreasing IL1B in DENV-infected BV2 cells. In addition, TRQ significantly attenuated weight loss, reduced clinical scores and extended the survival in DENV-infected ICR suckling mice. Critically, TRQ ameliorated pathological changes in ICR suckling mice brain by inhibiting microglia and NLRP3 activation and decreasing the production of inflammatory factors and the number of dead neurons. Conclusion: TRQ exerts potent inhibitory effects on dengue encephalitis in vitro and in vivo by reducing DENV-2-induced microglial activation and subsequently decreasing the inflammatory response, thereby protecting neurons. These findings demonstrate the potential of TRQ in the treatment of dengue encephalitis. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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47. Green-synthesized silver nanoparticles from Zingiber officinale extract: antioxidant potential, biocompatibility, anti-LOX properties, and in silico analysis.
- Author
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Ongtanasup, Tassanee, Kamdenlek, Patipat, Manaspon, Chawan, and Eawsakul, Komgrit
- Subjects
SILVER analysis ,COSMETICS ,IN vitro studies ,GINGER ,FLAVONOIDS ,ANTI-inflammatory agents ,ANTIOXIDANTS ,ORGANIC compounds ,CELL survival ,GAS chromatography ,ELECTRON microscopy ,MASS spectrometry ,PLANT extracts ,COMPUTER-assisted molecular modeling ,CELL lines ,NANOPARTICLES ,DRUG toxicity - Abstract
Introduction: Zingiber officinale extract has emerged as a compelling candidate for green synthesis of nanoparticles, offering diverse applications across medicine, cosmetics, and nutrition. This study delves into the investigation of in vitro toxicity and explores the biomedical utility of green-synthesized silver nanoparticles derived from ginger extract (GE-AgNPs). Methods: We employed established protocols to evaluate in vitro aspects such as antioxidant capacity, anti-inflammatory potential, and biocompatibility of GE-AgNPs. Additionally, molecular docking was employed to assess their anti-lipoxygenase (anti-LOX) activity. Results: Our findings highlight that the extraction of ginger extract at a pH of 6, utilizing a cosolvent blend of ethanol and ethyl acetate in a 1:1 ratio, yields heightened antioxidant capacity attributed to its rich phenolic and flavonoid content. In the context of silver nanoparticle synthesis, pH 6 extraction yields the highest quantity of nanoparticles, characterized by an average size of 32.64 ± 1.65 nm. Of particular significance, GE-AgNPs (at pH 6) demonstrated remarkable efficacy in scavenging free radicals, as evidenced by an IC
50 value of 6.83 ± 0.47 µg/mL. The results from the anti-LOX experiment indicate that GE-AgNPs, at a concentration of 10 µg/mL, can inhibit LOX activity by 25%, outperforming ginger extract which inhibits LOX by 17–18%. Notably, clionasterol exhibited higher binding energy and enhanced stability (-8.9 kcal/mol) compared to nordihydroguaiaretic acid. Furthermore, a cell viability study confirmed the safety of GE-AgNPs at a concentration of 17.52 ± 7.00 µg/mL against the L929 cell line. Conclusion: These comprehensive findings underscore the significant biomedical advantages of GE-AgNPs and emphasize their potential incorporation into cosmetic products at a maximum concentration of 10 µg/mL. [ABSTRACT FROM AUTHOR]- Published
- 2024
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48. Drug-resistant profiles of extracellular vesicles predict therapeutic response in TNBC patients receiving neoadjuvant chemotherapy.
- Author
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Kim, Min Woo, Lee, Hyojung, Lee, Suji, Moon, Sol, Kim, Young, Kim, Joon Ye, Kim, Seung Il, and Kim, Jee Ye
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EXTRACELLULAR vesicles ,NEOADJUVANT chemotherapy ,TRIPLE-negative breast cancer ,CELL lines ,GENE expression - Abstract
Background: Predicting tumor responses to neoadjuvant chemotherapy (NAC) is critical for evaluating prognosis and designing treatment strategies for patients with breast cancer; however, there are no reliable biomarkers that can effectively assess tumor responses. Therefore, we aimed to evaluate the clinical feasibility of using extracellular vesicles (EVs) to predict tumor response after NAC. Methods: Drug-resistant triple-negative breast cancer (TNBC) cell lines were successfully established, which developed specific morphologies and rapidly growing features. To detect resistance to chemotherapeutic drugs, EVs were isolated from cultured cells and plasma samples collected post-NAC from 36 patients with breast cancer. Results: Among the differentially expressed gene profiles between parental and drug-resistant cell lines, drug efflux transporters such as MDR1, MRP1, and BCRP were highly expressed in resistant cell lines. Drug efflux transporters have been identified not only in cell lines but also in EVs released from parental cells using immunoaffinity-based EV isolation. The expression of drug resistance markers in EVs was relatively high in patients with residual disease compared to those with a pathological complete response. Conclusions: The optimal combination of drug-resistant EV markers was significantly efficient in predicting resistance to NAC with 81.82% sensitivity and 92.86% specificity. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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- View/download PDF
49. Building in vitro tools for livestock genomics: chromosomal variation within the PK15 cell line.
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Johnsson, M., Hickey, J. M., and Jungnickel, M. K.
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FUNCTIONAL genomics ,GENOMICS ,CELL anatomy ,CELL culture ,GENE frequency ,TRISOMY ,CELL lines - Abstract
Background: Cultured porcine cell lines are powerful tools for functional genomics and in vitro phenotypic testing of candidate causal variants. However, to be utilised for genomic or variant interrogation assays, the genome sequence and structure of cultured cell lines must be realised. In this work, we called variants and used read coverage in combination with within-sample allele frequency to detect potential aneuploidy in two immortalised porcine kidney epithelial (PK15) cell lines and in a pig embryonic fibroblast line. Results: We compared two PK15 cultured cells samples: a new American Type Culture Collection (ATCC) sample and one that has been utilised and passaged within the laboratory for an extended period (> 10 years). Read coverage and within-sample allele frequencies showed that several chromosomes are fully or partially aneuploid in both PK15 lines, including potential trisomy of chromosome 4 and tetrasomy of chromosome 17. The older PK15 line showed evidence of additional structural variation and potentially clonal variation. By comparison, the pig embryonic fibroblast line was free from the gross aneuploidies seen in the PK15s. Conclusions: Our results show that the PK15 cell lines examined have aneuploidies and complex structural variants in their genomes. We propose that screening for aneuploidy should be considered for cell lines, and discuss implications for livestock genomics. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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- View/download PDF
50. Gene expression signature predicts radiation sensitivity in cell lines using the integral of dose–response curve.
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Kolnohuz, Alona, Ebrahimpour, Leyla, Yolchuyeva, Sevinj, and Manem, Venkata S. K.
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LINE integrals ,PHYSIOLOGICAL effects of radiation ,GENE expression ,CELL lines ,RADIATION - Abstract
Background: Although substantial efforts have been made to build molecular biomarkers to predict radiation sensitivity, the ability to accurately stratify the patients is still limited. In this study, we aim to leverage large-scale radiogenomics datasets to build genomic predictors of radiation response using the integral of the radiation dose–response curve. Methods: Two radiogenomics datasets consisting of 511 and 60 cancer cell lines were utilized to develop genomic predictors of radiation sensitivity. The intrinsic radiation sensitivity, defined as the integral of the dose–response curve (AUC) was used as the radioresponse variable. The biological determinants driving AUC and SF2 were compared using pathway analysis. To build the predictive model, the largest and smallest datasets consisting of 511 and 60 cancer cell lines were used as the discovery and validation cohorts, respectively, with AUC as the response variable. Results: Utilizing a compendium of three pathway databases, we illustrated that integral of the radiobiological model provides a more comprehensive characterization of molecular processes underpinning radioresponse compared to SF2. Furthermore, more pathways were found to be unique to AUC than SF2—30, 288 and 38 in KEGG, REACTOME and WIKIPATHWAYS, respectively. Also, the leading-edge genes driving the biological pathways using AUC were unique and different compared to SF2. With regards to radiation sensitivity gene signature, we obtained a concordance index of 0.65 and 0.61 on the discovery and validation cohorts, respectively. Conclusion: We developed an integrated framework that quantifies the impact of physical radiation dose and the biological effect of radiation therapy in interventional pre-clinical model systems. With the availability of more data in the future, the clinical potential of this signature can be assessed, which will eventually provide a framework to integrate genomics into biologically-driven precision radiation oncology. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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- View/download PDF
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