22 results on '"Yin, Tongming"'
Search Results
2. Genome-wide identification and analysis of the molecular evolution and expression of type-A response regulator genes in Populus deltoids
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Lu, Jing, Wei, Suyun, Yin, Tongming, and Chen, Yingnan
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- 2023
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3. Natural shikonin and acetyl-shikonin improve intestinal microbial and protein composition to alleviate colitis-associated colorectal cancer
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Lin, Hongyan, Ma, Xiaopeng, Yang, Xiaorong, Chen, Qingqing, Wen, Zhongling, Yang, Minkai, Fu, Jiangyan, Yin, Tongming, Lu, Guihua, Qi, Jinliang, Han, Hongwei, and Yang, Yonghua
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- 2022
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4. Corrigendum to “Genome-wide identification and analysis of the molecular evolution and expression of type-A response regulator genes in Populus deltoides” [Ind. Crops Prod. 194 (2023) 116336]
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Lu, Jing, Wei, Suyun, Yin, Tongming, and Chen, Yingnan
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- 2024
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5. Fast orthogonal linear discriminant analysis with application to image classification
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Ye, Qiaolin, Ye, Ning, and Yin, Tongming
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- 2015
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6. In vitro production and antifungal activity of peptide ABP-dHC-cecropin A
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Zhang, Jiaxin, Movahedi, Ali, Xu, Junjie, Wang, Mengyang, Wu, Xiaolong, Xu, Chen, Yin, Tongming, and Zhuge, Qiang
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- 2015
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7. Flexible orthogonal semisupervised learning for dimension reduction with image classification
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Ye, Qiaolin, Ye, Ning, Zhao, Chunxia, Yin, Tongming, and Zhang, Haofeng
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- 2014
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8. A modified natural small molecule inhibits triple-negative breast cancer growth by interacting with Tubb3.
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Han, Hongwei, Yang, Minkai, Wen, Zhongling, Wang, Xuan, Lai, Xiaohui, Zhang, Yahan, Fang, Rongjun, Yin, Tongming, Yang, Xiaorong, Wang, Xiaoming, Zhao, Quan, Qi, Jinliang, Chen, Hongyuan, Lin, Hongyan, and Yang, Yonghua
- Abstract
Triple-negative breast cancer (TNBC) is a malignant tumor without specific therapeutic targets and a poor prognosis. Chemotherapy is currently the first-line therapeutic option for TNBC. However, due to the heterogeneity of TNBC, not all of TNBC patients are responsive to chemotherapeutic agents. Therefore, the demand for new targeted agents is critical. β -tubulin isotype III (Tubb3) is a prognostic factor associated with cancer progression, including breast cancer, and targeting Tubb3 may lead to improve TNBC disease control. Shikonin, the active compound in the roots of Lithospermun erythrorhizon suppresses the growth of various types of tumors, and its efficacy can be improved by altering its chemical structure. In this work, the anti-TNBC effect of a shikonin derivative (PMMB276) was investigated, and its mechanism was also investigated. This study combines flow cytometry, immunofluorescence staining, immunoblotting, immunoprecipitation, siRNA silencing, and the iTRAQ proteomics assay to analyze the inhibition potential of PMMB276 on TNBC. In vivo study was performed, Balb/c female murine models with or without the small molecule treatments. Herein, we screened 300 in-house synthesized analogs of shikonin against TNBC and identified a novel small molecule, PMMB276; it suppressed cell proliferation, induced apoptosis, and arrested the cell cycle at the G2/M phase, suggesting that it could have a tumor suppressive role in TNBC. Tubb3 was identified as the target of PMMB276 using proteomic and biological activity analyses. Meanwhile, PMMB276 regulated microtubule dynamics in vitro by inducing microtubule depolymerization and it could act as a tubulin stabilizer by a different process than that of paclitaxel. Moreover, suppressing or inhibiting Tubb3 with PMMB276 reduced the growth of breast cancer in an experimental mouse model, indicating that Tubb3 plays a significant role in TNBC progression. The findings support the therapeutic potential of PMMB276, a Tubb3 inhibitor, as a treatment for TNBC. Our findings might serve as a foundation for the utilization of shikonin and its derivatives in the development of anti-TNBC. A small novel molecule, i.e., α-lipoic acyl shikonin, modified form of a natural product (shikonin), acts as a novel inhibitor of Tubb3. [Display omitted] [ABSTRACT FROM AUTHOR]
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- 2024
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9. Enhanced multi-weight vector projection support vector machine
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Ye, Qiaolin, Ye, Ning, and Yin, Tongming
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- 2014
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10. Recursive Dimension Reduction for semisupervised learning.
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Ye, Qiaolin, Yin, Tongming, Gao, Shangbing, Jing, Jiajia, Zhang, Yu, and Sun, Cuiping
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RECURSIVE functions , *DIMENSION reduction (Statistics) , *LEARNING , *ITERATIVE methods (Mathematics) , *SUBSPACES (Mathematics) - Abstract
Semisupervised Dimension Reduction (SDR) Using Trace Ratio Criterion (TR-FSDA) is an effective iterative SDR algorithm, which introduces a flexible regularization term ‖ F − X T W ‖ 2 to relax such a hard linear constraint in SDA that the low-dimensional representation F is constrained to lie in the linear subspace spanned by the data matrix X . We, however, observe that TR-FSDA may take some meaningless features in the iteration and cannot be always guaranteed to converge. In this paper, we propose a novel method for SDR, referred to as Recursive Dimension Reduction for Semisupervised Learning (RDS). Instead of solving the non-trivial TR problem using the iterative algorithm of TR-FSDA, we solve the objective function of TR-FSDA using a newly-developed recursive procedure. In each iteration, only a projection vector and a one-dimensional data representation are produced by solving a standard Rayleigh Quotient problem. Our algorithm escapes from the convergence guarantee, since it directly solves the objective and requires no any iterative strategy in finding each of the projection vectors. The experiments on four face databases, one object database, one shape image database, and one Handwritten Digit database demonstrate the effectiveness of RDS. [ABSTRACT FROM AUTHOR]
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- 2016
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11. Novel shikonin derivative suppresses tumor growth and metastasis intervention of Wnt/β-catenin pathway.
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Han, Hongwei, Wen, Zhongling, Lai, Xiaohui, Yang, Minkai, Fu, Jiangyan, Yang, Liangjie, Chen, Qingqing, Ma, Yudi, Jie, Wencai, Wang, Changyi, Yin, Tongming, Lu, Guihua, Wang, Xiaoming, Sun, Shucun, Zhao, Quan, Qi, Jinliang, Lin, Hongyan, and Yang, Yonghua
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SHIKONIN , *WNT signal transduction , *CATENINS , *METASTASIS , *TUMOR growth , *CANCER cell migration , *CANCER cell proliferation - Abstract
Colorectal cancer is a common malignancy and the second leading cause of cancer-related death. Emerging evidence suggests that the Wnt/β-catenin pathway has a significant role in cancer development. Shikonin is one of the main bioactive components of the plant, Lithospermum erythrorhizon, which possesses various biological properties. In this study, we identified a shikonin derivative, E5, as a novel suppressor of colorectal carcinoma that acted by inhibiting cell proliferation and migration, and promoting apoptosis. Mechanistically, the drug activated caspase-dependent pathways, negatively regulating the Wnt/β-catenin pathway, and inhibited epithelial–mesenchymal transition. The findings suggest the potential of β-catenin as a molecular target in colon carcinoma and propose E5 as a promising therapeutic strategy for targeting Wnt/β-catenin [Display omitted] ● A novel thioether shikonin derivative (E5), modified form of shikonin, acts as a novel inhibitor of β-catenin. ● E5 suppressed cancer cell proliferation and migration and promoted cell apoptosis via caspase-dependent pathways. ● E5 can be a drug candidate and has the potential to inhibit Wnt/β-catenin signaling pathway in the colon carcinoma. [ABSTRACT FROM AUTHOR]
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- 2023
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12. Pathways to sex determination in plants: how many roads lead to Rome?
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Feng, Guanqiao, Sanderson, Brian J, Keefover-Ring, Ken, Liu, Jianquan, Ma, Tao, Yin, Tongming, Smart, Lawrence B, DiFazio, Stephen P, and Olson, Matthew S
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SEX in plants , *MOLECULAR evolution , *FLOWER development , *CELLULAR signal transduction , *CYTOKININS , *SHARED workspaces , *ANGIOSPERMS - Abstract
The presence of thousands of independent origins of dioecy in angiosperms provides a unique opportunity to address the parallel evolution of the molecular pathways underlying unisexual flowers. Recent progress towards identifying sex determination genes has identified hormone response pathways, mainly associated with cytokinin and ethylene response pathways, as having been recruited multiple times independently to control unisexuality. Moreover, transcriptomics has begun to identify commonalities among intermediate sections of signal transduction pathways. These recent advances set the stage for development of a comparative evolutionary development research program to identify the shared and unique aspects of the genetic pathways of unisexual flower development in angiosperms. [ABSTRACT FROM AUTHOR]
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- 2020
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13. Evaluation, characterization, expression profiling, and functional analysis of DXS and DXR genes of Populus trichocarpa.
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Xu, Chen, Wei, Hui, Movahedi, Ali, Sun, Weibo, Ma, Xiaoxing, Li, Dawei, Yin, Tongming, and Zhuge, Qiang
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BLACK cottonwood , *FUNCTIONAL analysis , *WOODY plants , *SALVIA miltiorrhiza , *POPLARS , *ABSCISIC acid - Abstract
1-Deoxy-D-xylulose-5-phosphate synthasse (DXS) and 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR) are key enzymes in terpenoid biosynthesis. DXS catalyzes the formation of 1-deoxy-D-xylulose 5-phosphate (DXP) from pyruvate and D-glyceraldehyde-3-phosphate. DXR catalyzes the formation of 2-C-methyl-D-erythritol 4-phosphate (MEP) from DXP. Previous studies of the DXS and DXR genes have focused on herbs, such as Arabidopsis thaliana , Salvia miltiorrhiza , and Amomum villosum , but few studies have been conducted on woody plants. For that reason, we chose Populus trichocarpa as a model woody plant for investigating the DXS and DXR genes. PtDXS exhibited the highest expression level in leaves and the lowest expression in roots. PtDXR showed maximum expression in young leaves, and the lowest expression in mature leaves. The expression profiles revealed by RT-PCR following different elicitor treatments such as abscisic acid, NaCl, PEG 6000 , H 2 O 2 , and cold stress showed that PtDXS and PtDXR were elicitor-responsive genes. Our results showed that the PtDXS gene exhibited diurnal changes, but PtDXR did not. Moreover, overexpression of PtDXR in transgenic poplars improved tolerance to abiotic and biotic stresses. Those results showed that the PtDXR encoded a functional protein, and widely participates in plant growth and development, stress physiological process. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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14. Function and molecular mechanism of a poplar placenta limited MIXTA gene in regulating differentiation of plant epidermal cells.
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Zhou, Fangwei, Wu, Huaitong, Chen, Yingnan, Wang, Mingxiu, Tuskan, Gerald A., and Yin, Tongming
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PLANT cell differentiation , *POPLARS , *PLACENTA , *IN situ hybridization , *CARPEL - Abstract
The placenta in fruits of most plants either desiccate and shrink as the fruits mature or develop further to form the fleshy tissues. In poplars, placental epidermal cells protrude collectively to produce catkin fibers. In this study, three carpel limited MIXTA genes, PdeMIXTA02, PdeMIXTA03, PdeMIXTA04 , were find to specifically expressed in carpel immediately after pollination. Heterologous expression of the three genes in Arabidopsis demonstrated that PdeMIXTA04 significantly promoted trichomes density and could restore trichomes in the trichomeless mutant. By contrast, such functions were not observed with PdeMIXTA02, PdeMIXTA03. In situ hybridization revealed that PdeMIXTA04 was explicitly expressed in poplar placental epidermal cells. We also confirmed trichome-specific expression of the PdeMIXTA04 promoter. Multiple experimental proofs have confirmed the interaction between PdeMIXTA04, PdeMYC and PdeWD40, indicating PdeMIXTA04 functioned through the MYB-bHLH-WD40 ternary complex. Our work provided distinctive understanding of the molecular mechanism triggering differentiation of poplar catkins. [ABSTRACT FROM AUTHOR]
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- 2023
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15. Functional analyses of PtRDM1 gene overexpression in poplars and evaluation of its effect on DNA methylation and response to salt stress.
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Movahedi, Ali, Zhang, Jiaxin, Sun, Weibo, Mohammadi, Kourosh, Almasi Zadeh Yaghuti, Amir, Wei, Hui, Wu, Xiaolong, Yin, Tongming, and Zhuge, Qiang
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POPLAR genetics , *DNA methylation , *EFFECT of salts on plants , *NUCLEOTIDE sequence , *HETEROCHROMATIN - Abstract
Epigenetic modification by DNA methylation is necessary for all cellular processes, including genetic expression events, DNA repair, genomic imprinting and regulation of tissue development. It occurs almost exclusively at the C5 position of symmetric CpG and asymmetric CpHpG and CpHpH sites in genomic DNA. The RNA-directed DNA methylation ( RDM1 ) gene is crucial for heterochromatin and DNA methylation. We overexpressed PtRDM1 gene from Populus trichocarpa to amplify transcripts of orthologous RDM1 in ‘Nanlin895’ ( P. deltoides × P. euramericana ‘Nanlin895’). This overexpression resulted in increasing RDM1 transcript levels: by ∼150% at 0 mM NaCl treatment and by ∼300% at 60 mM NaCl treatment compared to WT (control) poplars. Genomic cytosine methylation was monitored within 5.8S rDNA and histone H3 loci by bisulfite sequencing. In total, transgenic poplars revealed more DNA methylation than WT plants. In our results, roots revealed more methylated CG contexts than stems and leaves whereas, histone H3 presented more DNA methylation than 5.8S rDNA in both WT and transgenic poplars. The NaCl stresses enhanced more DNA methylation in transgenic poplars than WT plants through histone H3 and 5.8 rDNA loci. Also, the overexpression of PtRDM1 resulted in hyper-methylation, which affected plant phenotype. Transgenic poplars revealed significantly more regeneration of roots than WT poplars via NaCl treatments. Our results proved that RDM1 protein enhanced the DNA methylation by chromatin remodeling (e.g. histone H3 ) more than repetitive DNA sequences (e.g. 5.8S rDNA). [ABSTRACT FROM AUTHOR]
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- 2018
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16. Functional analyses of NDPK2 in Populus trichocarpa and overexpression of PtNDPK2 enhances growth and tolerance to abiotic stresses in transgenic poplar.
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Zhang, Jiaxin, Movahedi, Ali, Sang, Ming, Wei, Zhiheng, Xu, Junjie, Wang, Xiaoli, Wu, Xiaolong, Wang, Mengyang, Yin, Tongming, and Zhuge, Qiang
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NUCLEOSIDE diphosphate kinases , *EUKARYOTIC cells , *AUTOPHOSPHORYLATION , *ARABIDOPSIS thaliana , *POPLAR genetics - Abstract
Nucleoside diphosphate kinases (NDPKs) are multifunctional proteins that regulate a variety of eukaryotic cellular activities, including cell proliferation, development, and differentiation. NDPK2 regulates the expression of antioxidant genes in plants. In a previous study, the Arabidopsis thaliana NDPK2 gene ( AtNDPK2 ) was found to be associated with H 2 O 2 -mediated mitogen-activated protein kinase signaling in Arabidopsis thaliana . Proteins from transgenic plants overexpressing AtNDPK2 showed higher levels of autophosphorylation and NDPK activity and lower levels of reactive oxygen species (ROS) than those of wild-type (WT) plants. Therefore, constitutive overexpression of AtNDPK2 in Arabidopsis plants conferred enhanced tolerance to multiple environmental stresses that elicit ROS accumulation in situ . In this study, we cloned the Populus trichocarpa NDPK2 gene and analyzed its molecular structure and function. We generated and evaluated transgenic poplar plants expressing the PtNDPK2 gene under the control of the 35S promoter to achieve enhanced tolerance to various abiotic stresses. Transgenic poplar plants showed enhanced tolerance to salt and drought stress at the whole-plant level. The transgenic poplar plants showed significantly greater tolerance to 200 mM NaCl and drought stresses than WT poplar plants. In addition, the transgenic plants exhibited better growth due to increased expression of auxin-related indole acetic acid genes under normal growth conditions compared with WT plants. Our results suggest that induction of PtNDPK2 overexpression in poplars will be useful for increasing biomass production in the presence of various abiotic stresses. [ABSTRACT FROM AUTHOR]
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- 2017
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17. PKM2/PDK1 dual-targeted shikonin derivatives restore the sensitivity of EGFR-mutated NSCLC cells to gefitinib by remodeling glucose metabolism.
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Lin, Hongyan, Han, Hongwei, Yang, Minkai, Wen, Zhongling, Chen, Qingqing, Ma, Yudi, Wang, Xuan, Wang, Changyi, Yin, Tongming, Wang, Xiaoming, Lu, Guihua, Chen, Hongyuan, Qi, Jinliang, and Yang, Yonghua
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GLYCOLYSIS , *PYRUVATE dehydrogenase kinase , *GLUCOSE metabolism , *SHIKONIN , *PYRUVATE kinase , *NON-small-cell lung carcinoma , *PYRUVATES - Abstract
Pyruvate kinase 2 (PKM2) and pyruvate dehydrogenase kinase 1 (PDK1) are two key enzymes in tumor glucose metabolism pathway that not only promote tumor growth and proliferation through accelerating aerobic glycolysis, but also contribute to drug resistance of non-small cell lung cancer (NSCLC). Considering that targeting PKM2 or PDK1 alone seems insufficient to remodel abnormal glucose metabolism to achieve significant antitumor activity, we proposed a "two-step approach" that regulates PKM2 and PDK1 synchronously. Firstly, we found that the combination of ML265 (PKM2 activator) and AZD7545 (PDK1 inhibitor) could synergistically inhibit proliferation and induce apoptosis in H1299 cells. Base on this, we designed a series of novel shikonin (SK) thioether derivatives as PKM2/PDK1 dual-target agents, among which the most potent compound E5 featuring a 2-methyl substitution on the benzene ring exerted significantly increased inhibitory activity toward EGFR mutant NSCLC cell H1975 (IC 50 = 1.51 μmol/L), which was 3 and 17-fold more active than the lead compound SK (IC 50 = 4.56 μmol/L) and the positive control gefitinib (IC 50 = 25.56 μmol/L), respectively. Additionally, E5 also showed good anti-tumor activity in xenografted mouse models, with significantly lower toxicity side effects than SK. Moreover, E5 also inhibited the entry of PKM2 into nucleus to regulate the transcriptional activation of oncogenes, thus restoring the sensitivity of H1975 cell to gefitinib. Collectively, these data demonstrate that E5 , a dual inhibitor of PKM2/PDK1, may be a promising adjunct to gefitinib in the treatment of EGFR-TKIs resistant NSCLC, deserving further investigation. [Display omitted] • A synergistic effect of PKM2 activation and PDK1 inhibition was first demonstrated. • A series of PKM2/PDK1 dual-target shikonin thioether derivatives were developed. • The most active compound E5 significantly inhibit tumor growth in vitro and in vivo. • The most active compound E5 enhance the sensitivity of H1975 cells to gefitinib. [ABSTRACT FROM AUTHOR]
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- 2023
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18. Novel shikonin derivatives suppress cell proliferation, migration and induce apoptosis in human triple-negative breast cancer cells via regulating PDK1/PDHC axis.
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Chen, Qingqing, Han, Hongwei, Lin, Faxiang, Yang, Liangjie, Feng, Lu, Lai, Xiaohui, Wen, Zhongling, Yang, Minkai, Wang, Changyi, Ma, Yudi, Yin, Tongming, Lu, Guihua, Lin, Hongyan, Qi, Jinliang, and Yang, Yonghua
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TRIPLE-negative breast cancer , *CANCER cells , *SHIKONIN , *CELL proliferation , *CELL migration , *CELL cycle - Abstract
PDK1 is one of the key enzymes in the glucose metabolism pathway, which is abnormally high expressed in breast cancer tissues and can promote tumor proliferation and metastasis. PDK1 and the PDHC/PDK axis are important targets for regulating glucose metabolism and anti-tumor activity. In this study, we evaluated the anti-tumor activities of a series of semi-synthesized shikonin (SK) derivatives against human breast cancer cells. The anti-proliferation activity of SK derivatives against human breast cancer cell lines was tested by CCK-8 and EdU assay. Flow cytometry was utilized to evaluate cell apoptosis, reactive oxygen species and cell cycle distribution. Cell migration ability was determined by wound healing and trans-well assay. PDK1 targeting effect was confirmed by western bolting, molecular docking, bio-layer interferometry and PDK1 enzyme activity assay. Nude-mouse transplanted tumor model was used to evaluate their anti-tumor effect in vivo. Findings revealed that SK derivatives had good anti-proliferation ability against MDA-MB-231 cell. They induced cell apoptosis by regulating the mitochondrial apoptosis and death receptor pathway. They also inhibited cell migration by suppressing EMT progression. Molecular docking, PDK1 affinity and enzyme activity demonstrated their PDK1 targeting. In vivo antitumor experiment showed that E2 could significantly inhibit tumor growth with lower side-effect on mice than SK. In conclusion, the novel SK derivatives E2 and E5 inhibited tumor glycolysis by targeting PDK1 and ultimately induced apoptosis. Our data demonstrated that E2 would be a good lead compound for the treatment of human TNBC as a novel PDK1 inhibitor. [ABSTRACT FROM AUTHOR]
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- 2022
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19. A weighted one-class support vector machine.
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Zhu, Fa, Yang, Jian, Gao, Cong, Xu, Sheng, Ye, Ning, and Yin, Tongming
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SUPPORT vector machines , *KNOWLEDGE management , *K-nearest neighbor classification , *DATA distribution , *PROBLEM solving - Abstract
The standard one-class support vector machine (OC-SVM) is sensitive to noises, since every instance is equally treated. To address this problem, the weighted one-class support vector machine (WOC-SVM) was presented. WOC-SVM weakens the impact of noises by assigning lower weights. In this paper, a novel instance-weighted strategy is proposed for WOC-SVM. The weight is only relevant to the neighbors׳ distribution knowledge, which is only decided by k -nearest neighbors. The closer to the boundary of the data distribution the instance is, the lower the corresponding weight is. The experimental results demonstrate that WOC-SVM outperforms the standard OC-SVM when using the proposed instance-weighted strategy. The proposed instance-weighted method performs better than previous ones. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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20. A novel inclusion complex (β-CD/ABP-dHC-cecropin A) with antibiotic propertiess for use as an anti-Agrobacterium additive in transgenic poplar rooting medium.
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Zhang, Jiaxin, Li, Jianfeng, Movahedi, Ali, Sang, Ming, Xu, Chen, Xu, Junjie, Wei, Zhiheng, Yin, Tongming, and Zhuge, Qiang
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INCLUSION compounds , *ANTIBIOTICS , *AGROBACTERIUM , *ADDITIVES , *DRUG development , *BIOCHEMICAL mechanism of action , *ANTIFUNGAL agents - Abstract
The increasing resistance of bacteria and fungi to currently available antibiotics is a major concern worldwide, leading to enormous effort to develop novel antibiotics with new modes of action.We recently reported that ABP-dHC-cecropin A exhibited strong antibacterial and antifungal activity, making it a candidate antibiotic substitute. In this study, β-cyclodextrin (β-CD) combined with ABP-dHC-cecropin A enhanced the physical and chemical properties of ABP-dHC-cecropin A but did not significantly decrease its antibacterial activity. Thus, β-CD/ABP-dHC-cecropin A should be considered a novel antibacterial drug. We used β-CD/ABP-dHC-cecropin A as an anti- Agrobacterium compound to supplementtransgenic poplar medium. Sideeffects of the inclusion complex had little impact on plantgrowth. Thus, β-CD/ABP-dHC-cecropin A may be used as traditional antibiotics forpoplar transplantation with greater antibbacterial effects. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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21. Molecular structure, chemical synthesis, and antibacterial activity of ABP-dHC-cecropin A from drury (Hyphantria cunea).
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Zhang, Jiaxin, Movahedi, Ali, Wang, Xiaoli, Wu, Xiaolong, Yin, Tongming, and Zhuge, Qiang
- Subjects
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MOLECULAR structure , *CHEMICAL synthesis , *ANTIBACTERIAL agents , *HYPHANTRIA cunea , *ANTIBIOTICS , *ANTISENSE DNA - Abstract
The increasing resistance of bacteria and fungi to currently available antibiotics is a major concern worldwide, leading to enormous efforts to develop new antibiotics with new modes of actions. In this paper, cDNA encoding cecropin A was amplified from drury ( Hyphantria cunea ) ( dHC ) pupa fatbody total RNA using RT-PCR. The full-length dHC -cecropin A cDNA encoded a protein of 63 amino acids with a predicted 26-amino acid signal peptide and a 37-amino acid functional domain. We synthesized the antibacterial peptide (ABP) from the 37-amino acid functional domain (ABP- dHC -cecropin A), and amidated it via the C-terminus. Time-of-flight mass spectrometry showed its molecular weight to be 4058.94. The ABP- dHC -cecropin A was assessed in terms of its protein structure using bioinformatics and CD spectroscopy. The protein's secondary structure was predicted to be α-helical. In an antibacterial activity analysis, the ABP- dHC -cecropin A exhibited strong antibacterial activity against E. coli K12D31 and Agrobacterium EHA105. [ABSTRACT FROM AUTHOR]
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- 2015
- Full Text
- View/download PDF
22. Shikonin N-benzyl matrinic acid ester derivatives as novel telomerase inhibitors with potent activity against lung cancer cell lines.
- Author
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Han, Hongwei, He, Cong, Chen, Xingyu, Luo, Yuelin, Yang, Minkai, Wen, Zhongling, Hu, Jiabao, Lin, Faxiang, Han, Mi, Yin, Tongming, Yang, Rongwu, Lin, Hongyan, Qi, Jinliang, and Yang, Yonghua
- Subjects
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ESTER derivatives , *ACID derivatives , *CANCER cells , *TELOMERASE , *SHIKONIN , *CELL death , *TELOMERASE reverse transcriptase , *LUNG cancer - Abstract
PMMB-302 has an effect on the expression of apoptosis-related proteins such as Bcl2, Bcl-XL, caspase-9, caspase3 and FADD. Moreover, PMMB-302 inhibited expression of telomerase core proteins, dyskerin and NHP2, and telomerase reverse transcriptase RNA. These results suggested that PMMB-302 has tumor suppressive roles in lung cancer cells. [Display omitted] • A small novel molecule modified form of a natural product (shikonin), acts as a novel inhibitor of telomerase. • The small molecule suppresses cancer cell proliferation in vitro via inducing apoptosis and arresting cell cycle at G2/M phase. • This small molecule induces apoptosis in A549 cells through the mitochondrial and death receptor pathways. In this study, a series of novel shikonin N -benzyl matrinic acid ester derivatives (PMMB-299–PMMB-310) were synthesized and tested for their ability to inhibit the proliferation of cancer cells. Compared with shikonin and matrine, some of the ester derivatives were found to exhibit better anti-proliferative activity against seven different cancer cell lines, with less cytotoxicity toward non-cancerous cells. The strongest anti-proliferative activity was exhibited by PMMB-302, which had an IC 50 value of 2.71 μM against A549 cells. The compound caused cell cycle arrest in the G2/M phase and induced apoptosis. Effects on the expression of apoptosis-related molecules such as Bcl2, Bcl-XL, caspase-3, caspase-9 and FADD suggested that PMMB-302 has tumor suppressive roles in lung cancer cells. In addition, PMMB-302 inhibited expression of telomerase core proteins, dyskerin and NHP2, and telomerase reverse transcriptase RNA. Moreover, molecular docking of PMMB-302 was subsequently conducted to determine the probable binding mode with telomerase. Taken together, the results indicate that PMMB-302 acts as a tumor suppressor in lung cancer cells by negatively regulating telomerase expression. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
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