10 results on '"Zheng JK"'
Search Results
2. Inhibition of the Replication of Hepatitis B Virus In Vitroby Oxymatrine
- Author
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Lin, M, Yang, LY, Li, WY, Peng, YP, and Zheng, JK
- Abstract
This study investigated the inhibitory capacity of oxymatrine on in vitrohepatitis B virus (HBV) replication. HepG2.2.15 cells were treated with oxymatrine 50, 100, 200, 400, 800 or 1000 mg/l, or with human interferon-α2b (IFN-α2b 1000 U/l) as a positive control. Levels of hepatitis B surface antigen (HBsAg), hepatitis B e antigen (HBeAg) and HBV-DNA in cell supernatants were determined by enzyme-linked immunosorbent assay and fluorescent quantitative-polymerase chain reaction, respectively. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, flow cytometric analysis and terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick-end labelling were used to evaluate the cytotoxicity of oxymatrine. The inhibitory effects of oxymatrine gradually increased as the concentration increased from 200 to 1000 mg/l for HBsAg and HBeAg, and from 200 to 400 mg/l for HBV-DNA. There was no inhibitory effect of oxymatrine at concentrations < 200 mg/l. No significant difference was seen between human IFN-α2b (positive control) and oxymatrine ≥ 200 mg/l. It is concluded that oxymatrine can inhibit in vitroHBV replication and antigen expression at concentrations ≥ 200 mg/l.
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- 2009
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3. Secreted PTEN binds PLXDC2 on macrophages to drive antitumor immunity and tumor suppression.
- Author
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Zhang C, Ma HM, Wu S, Shen JM, Zhang N, Xu YL, Li CX, He P, Ge MK, Chu XL, Zhang YX, Zheng JK, Chen GQ, and Shen SM
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- Animals, Mice, Humans, Mice, Inbred C57BL, Signal Transduction drug effects, Neoplasms immunology, Neoplasms metabolism, Neoplasms pathology, Cell Line, Tumor, Tumor-Associated Macrophages metabolism, Tumor-Associated Macrophages immunology, Tumor-Associated Macrophages drug effects, Female, CD8-Positive T-Lymphocytes immunology, CD8-Positive T-Lymphocytes metabolism, Immunotherapy methods, PTEN Phosphohydrolase metabolism, PTEN Phosphohydrolase genetics, Tumor Microenvironment immunology, Tumor Microenvironment drug effects, Macrophages metabolism, Macrophages immunology
- Abstract
Loss of phosphatase and tensin homolog (PTEN) has been linked to an immunosuppressive tumor microenvironment, but its underlying mechanisms remain largely enigmatic. Here, we report that PTEN can be secreted by the transmembrane emp24 domain-containing protein 10 (TMED10)-channeled protein secretion pathway. Inhibiting PTEN secretion from tumor cells contributes to immunosuppression and impairs the tumor-suppressive role of PTEN, while intratumoral injection of PTEN protein promotes antitumor immunity and suppresses tumor growth in mice. Mechanistically, extracellular PTEN binds to the plexin domain-containing protein 2 (PLXDC2) on macrophages, triggering subsequent activation of JAK2-STAT1 signaling, which switches tumor-associated macrophages (TAMs) from the immunosuppressive to inflammatory phenotype, leading to enhanced activation of CD8
+ T and natural killer cells. Importantly, PTEN treatment also enhances the therapeutic efficacy of anti-PD-1 treatment in mice and reverses the immune-suppressive phenotype of patient-derived primary TAMs. These data identify a cytokine-like role of PTEN in immune activation and tumor suppression and demonstrate the therapeutic potential for extracellular administration of PTEN in cancer immunotherapy., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2024 Elsevier Inc. All rights reserved.)- Published
- 2024
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4. ANP32B-mediated repression of p53 contributes to maintenance of normal and CML stem cells.
- Author
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Yang S, Zhu XN, Zhang HL, Yang Q, Wei YS, Zhu D, Liu MD, Shen SM, Xia L, He P, Ge MK, Pan YL, Zhao M, Wu YL, Zheng JK, Chen GQ, and Yu Y
- Subjects
- Animals, Cell Cycle Proteins genetics, Cells, Cultured, Gene Expression Regulation, Leukemic, Hematopoietic Stem Cells metabolism, Hematopoietic Stem Cells pathology, Leukemia, Myelogenous, Chronic, BCR-ABL Positive genetics, Leukemia, Myelogenous, Chronic, BCR-ABL Positive metabolism, Mice, Neoplastic Stem Cells metabolism, Nerve Tissue Proteins genetics, Nuclear Proteins genetics, Tumor Suppressor Protein p53 genetics, Cell Cycle Proteins metabolism, Leukemia, Myelogenous, Chronic, BCR-ABL Positive pathology, Neoplastic Stem Cells pathology, Nerve Tissue Proteins metabolism, Nuclear Proteins metabolism, Tumor Suppressor Protein p53 metabolism
- Abstract
Proper regulation of p53 signaling is critical for the maintenance of hematopoietic stem cells (HSCs) and leukemic stem cells (LSCs). The hematopoietic cell-specific mechanisms regulating p53 activity remain largely unknown. Here, we demonstrate that conditional deletion of acidic leucine-rich nuclear phosphoprotein 32B (ANP32B) in hematopoietic cells impairs repopulation capacity and postinjury regeneration of HSCs. Mechanistically, ANP32B forms a repressive complex with p53 and thus inhibits the transcriptional activity of p53 in hematopoietic cells, and p53 deletion rescues the functional defect in Anp32b-deficient HSCs. Of great interest, ANP32B is highly expressed in leukemic cells from patients with chronic myelogenous leukemia (CML). Anp32b deletion enhances p53 transcriptional activity to impair LSC function in a murine CML model and exhibits synergistic therapeutic effects with tyrosine kinase inhibitors in inhibiting CML propagation. In summary, our findings provide a novel strategy to enhance p53 activity in LSCs by inhibiting ANP32B and identify ANP32B as a potential therapeutic target in treating CML., (© 2021 by The American Society of Hematology.)
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- 2021
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5. Targeting USP47 overcomes tyrosine kinase inhibitor resistance and eradicates leukemia stem/progenitor cells in chronic myelogenous leukemia.
- Author
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Lei H, Xu HZ, Shan HZ, Liu M, Lu Y, Fang ZX, Jin J, Jing B, Xiao XH, Gao SM, Gao FH, Xia L, Yang L, Liu LG, Wang WW, Liu CX, Tong Y, Wu YZ, Zheng JK, Chen GQ, Zhou L, and Wu YL
- Subjects
- Animals, Cell Proliferation drug effects, DNA Damage, DNA Repair drug effects, Extracellular Signal-Regulated MAP Kinases metabolism, Fusion Proteins, bcr-abl, Gene Expression Regulation, Leukemic drug effects, Humans, K562 Cells, Leukemia, Myelogenous, Chronic, BCR-ABL Positive genetics, Mice, Knockout, Proteasome Endopeptidase Complex metabolism, Protein Binding drug effects, Protein Stability drug effects, Proteolysis drug effects, RNA, Messenger genetics, RNA, Messenger metabolism, STAT5 Transcription Factor metabolism, Signal Transduction drug effects, Thiophenes pharmacology, Xenograft Model Antitumor Assays, Y-Box-Binding Protein 1 metabolism, ras Proteins metabolism, Mice, Drug Resistance, Neoplasm drug effects, Leukemia, Myelogenous, Chronic, BCR-ABL Positive pathology, Neoplastic Stem Cells metabolism, Neoplastic Stem Cells pathology, Protein Kinase Inhibitors pharmacology, Ubiquitin Thiolesterase metabolism, Ubiquitin-Specific Proteases metabolism
- Abstract
Identifying novel drug targets to overcome resistance to tyrosine kinase inhibitors (TKIs) and eradicating leukemia stem/progenitor cells are required for the treatment of chronic myelogenous leukemia (CML). Here, we show that ubiquitin-specific peptidase 47 (USP47) is a potential target to overcome TKI resistance. Functional analysis shows that USP47 knockdown represses proliferation of CML cells sensitive or resistant to imatinib in vitro and in vivo. The knockout of Usp47 significantly inhibits BCR-ABL and BCR-ABL
T315I -induced CML in mice with the reduction of Lin- Sca1+ c-Kit+ CML stem/progenitor cells. Mechanistic studies show that stabilizing Y-box binding protein 1 contributes to USP47-mediated DNA damage repair in CML cells. Inhibiting USP47 by P22077 exerts cytotoxicity to CML cells with or without TKI resistance in vitro and in vivo. Moreover, P22077 eliminates leukemia stem/progenitor cells in CML mice. Together, targeting USP47 is a promising strategy to overcome TKI resistance and eradicate leukemia stem/progenitor cells in CML.- Published
- 2021
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6. Nitrogen distribution and cycling through water flows in a subtropical bamboo forest under high level of atmospheric deposition.
- Author
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Tu LH, Hu TX, Zhang J, Huang LH, Xiao YL, Chen G, Hu HL, Liu L, Zheng JK, Xu ZF, and Chen LH
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- China, Ecosystem, Environmental Monitoring, Nitrogen metabolism, Rain, Seasons, Trees physiology, Tropical Climate, Water, Nitrogen chemistry, Nitrogen Cycle, Plant Leaves metabolism, Plant Roots metabolism, Sasa metabolism, Soil chemistry
- Abstract
Background: The hydrological cycle is an important way of transportation and reallocation of reactive nitrogen (N) in forest ecosystems. However, under a high level of atmospheric N deposition, the N distribution and cycling through water flows in forest ecosystems especially in bamboo ecosystems are not well understood., Methodology/principal Findings: In order to investigate N fluxes through water flows in a Pleioblastus amarus bamboo forest, event rainfall/snowfall (precipitation, PP), throughfall (TF), stemflow (SF), surface runoff (SR), forest floor leachate (FFL), soil water at the depth of 40 cm (SW1) and 100 cm (SW2) were collected and measured through the whole year of 2009. Nitrogen distribution in different pools in this ecosystem was also measured. Mean N pools in vegetation and soil (0-1 m) were 351.7 and 7752.8 kg ha(-1). Open field nitrogen deposition at the study site was 113.8 kg N ha(-1) yr(-1), which was one of the highest in the world. N-NH4(+), N-NO3(-) and dissolved organic N (DON) accounted for 54%, 22% and 24% of total wet N deposition. Net canopy accumulated of N occurred with N-NO3(-) and DON but not N-NH4(+). The flux of total dissolved N (TDN) to the forest floor was greater than that in open field precipitation by 17.7 kg N ha(-1) yr(-1), due to capture of dry and cloudwater deposition net of canopy uptake. There were significant negative exponential relationships between monthly water flow depths and monthly mean TDN concentrations in PP, TF, SR, FFL and SW1., Conclusions/significance: The open field nitrogen deposition through precipitation is very high over the world, which is the main way of reactive N input in this bamboo ecosystem. The water exchange and N consume mainly occurred in the litter floor layer and topsoil layer, where most of fine roots of bamboo distributed.
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- 2013
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7. Prevalence and genotype distribution of human papillomavirus infections in women attending hospitals in Chaozhou of Guangdong province.
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Chen Q, Luo ZY, Lin M, Lin QL, Chen CY, Yang C, Xie LX, Li H, Zheng JK, Yang LY, and Ju GZ
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- Adolescent, Adult, Age Factors, Aged, Cervix Uteri pathology, China epidemiology, Coinfection, Confidence Intervals, Female, Humans, Logistic Models, Middle Aged, Odds Ratio, Prevalence, Vaginal Smears, Young Adult, Cervix Uteri virology, Genotype, Papillomaviridae genetics, Papillomavirus Infections epidemiology, Papillomavirus Infections virology
- Abstract
Background: Human papillomavirus (HPV) infection is the main cause of cervical cancer. Limited epidemiologic data of HPV prevalence are available for women attending hospitals in southern China. This study aimed to evaluate the profiles of HPV infection and cytology status in gynecological outpatients in Chaozhou City., Methods: A total of 2833 eligible women were enrolled. The HPV GenoArray test was used for HPV detection and genotyping. Nearly one half of the HPV positive women received liquid-based cytology test. Logistic regression analysis was performed to assess the predictable effects of age and genotype for categories of abnormal cytology., Results: The prevalence of overall, high-risk, and low-risk HPV infection were 24.5%, 19.5% and 8.4%, respectively. A U-shaped age-specific prevalence curve was observed in overall HPV and high- risk HPV, but not in low-risk HPV, which declined with age increasing. The 6 most common high-risk HPV type in descending order, were types 52, 16, 58, 18, 68, and 33. Age and HPV genotype were both important determinants of abnormal cytology incidence, the older women (>45 years) and those infected with HPV type 16 and/or 18 having the highest risk for abnormal cytology., Conclusion: Our findings support the hypothesis that second-generation HPV prophylactic vaccines including HPV-52 and -58 may offer higher protection for women residing in Chaozhou and neighboring cities in Guangdong.
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- 2012
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8. Epidemiologic characterization of human papillomavirus infection in rural Chaozhou, eastern Guangdong Province of China.
- Author
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Chen Q, Xie LX, Qing ZR, Li LJ, Luo ZY, Lin M, Zhang SM, Chen WZ, Lin BZ, Lin QL, Li H, Chen WP, Zheng PY, Mao LZ, Chen CY, Yang C, Zhan YZ, Liu XZ, Zheng JK, and Yang LY
- Subjects
- Adult, China, Cross-Sectional Studies, DNA, Viral analysis, Female, Genetic Variation, Humans, Middle Aged, Papillomavirus Infections virology, Polymerase Chain Reaction methods, Prevalence, Real-Time Polymerase Chain Reaction methods, Rural Population, Sequence Analysis, DNA, Treatment Outcome, Uterine Cervical Neoplasms metabolism, Papillomaviridae genetics, Papillomavirus Infections epidemiology, Uterine Cervical Neoplasms virology
- Abstract
Background: Human papilloma virus (HPV) infection was the main cause of cervical cancer. There were only a few reports and detailed data about epidemiological research of HPV infection in rural population of China., Materials and Methods: The cervical cells of rural Chaozhou women were collected, and multiplex real time PCR was firstly performed to detect high-risk HPV (HR-HPV) infection, which could detect 13 types of HR-HPV (types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, and 68). Then, HPV-positive samples were typed by HPV GenoArray test., Results: HR-HPV DNA was detected by multiplex real time-PCR in 3830 of 48559 cases (7.89%). There was a peak incidence in age of 55-60 years group, and a lower incidence in who lived in plain group compared with suburban, mountain and seashore group. 3380 cases of HPV positive sample were genotyped, 11.01% (372/3380) cases could not be classified, among the typed 3008 cases, 101 cases were identified without HR-HPV type infection, 2907 cases were infected with one HR-HPV type at least, the 6 most common HR-HPV types in descending order of infection, were type 52 (33.4%, 16 (20.95%), 58 (15.93%), 33 (9.94%), 68 (9.22%) and 18 (8.36%). The combined prevalence of HPV types 16 and 18 accounted for 28.52% of total infection. However, type 52 plus 58 presented 48.23% of total infection. 2209/2907 cases were infected with a single HPV type and 698/2907 cases were infected with multiple types, and multiple infection constituent ratio increased with age, with a peak incidence in age 55-60 years group., Conclusions: Our findings showed low prevalence of HPV vaccine types (16 and 18) and relatively high prevalence of HPV-52 and -58, support the hypothesis that the second-generation HPV vaccines including HPV-52 and -58 may offer higher protection for women in rural Guangdong Province.
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- 2012
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9. A new cytotoxic indole-3-ethenamide from the halotolerant fungus Aspergillus sclerotiorum PT06-1.
- Author
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Wang H, Zheng JK, Qu HJ, Liu PP, Wang Y, and Zhu WM
- Abstract
A new cytotoxic indole-3-ethenamide (1) and two known compounds, 7-(3-methylbut-2-enyl)-1H-indole-3-carbaldehyde (2) and emodin (3) were isolated and identified from the ethyl acetate extract of Aspergillus sclerotiorum PT06-1 in a hypersaline nutrient-rich medium. On the basis of spectroscopic analysis and amino-acid analysis, the new structure of 1 was determined to be (S,E)-3-methyl-2-(N- methylacetamido)-N-(2-(7-(3-methylbut-2-enyl)-1H-indol-3-yl)vinyl)butanamide within 3:1 ratio of rotamers along the acetamido single bond in DMSO-d(6) at room temperature. Compound 1 showed moderate cytotoxicity against A-549 cells and weak cytotoxicity against HL-60 cells with the IC(50) values of 3.0 and 27 μM, respectively. Compound 2 has been separated as natural product for the first time, and its NMR data were also reported for the first time in this study.
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- 2011
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10. Skeletal myogenesis by human embryonic stem cells.
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Zheng JK, Wang Y, Karandikar A, Wang Q, Gai H, Liu AL, Peng C, and Sheng HZ
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- Animals, Biomarkers metabolism, Cardiotoxins metabolism, Cell Differentiation physiology, Cell Line, Cell Lineage, Embryonic Stem Cells cytology, Humans, In Situ Hybridization, Mice, Mice, Inbred C57BL, Mice, Inbred NOD, Mice, SCID, Muscle, Skeletal cytology, Satellite Cells, Skeletal Muscle cytology, Transplantation Conditioning, Embryonic Stem Cells physiology, Muscle Development physiology, Muscle, Skeletal growth & development, Satellite Cells, Skeletal Muscle physiology, Transplantation, Heterologous
- Abstract
We have examined the myogenic potential of human embryonic stem (hES) cells in a xeno-transplantation animal model. Here we show that precursors differentiated from hES cells can undergo myogenesis in an adult environment and give rise to a range of cell types in the myogenic lineage. This study provides direct evidences that hES cells can regenerate both muscle and satellite cells in vivo and are another promising cell type for treating muscle degenerative disorders in addition to other myogenic cell types.
- Published
- 2006
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