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MicroRNA-194 protects against chronic hepatitis B-related liver damage by promoting hepatocyte growth via ACVR2B  期刊论文  

  • 编号:
    58db7ad1-78dc-46e6-b902-edd81104c8cb
  • 作者:
    Gao, Xue[1];Zhao, Pan[2];Hu, Jie[3,4];Zhu, Hongguang[5,6];Zhang, Jiming(张继明)[7]Zhou, Zhongwen(周仲文)[6]Zhao, Jingmin[1];Tang, Feng(唐峰)*[6]
  • 语种:
    English
  • 期刊:
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE ISSN:1582-4934 2018 年 22 卷 9 期 (4534 - 4544) ; SEP
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  • 摘要:

    Persistent infection with the hepatitis B virus leads to liver cirrhosis and hepatocellular carcinoma. MicroRNAs (miRNAs) play an important role in a variety of biological processes; however, the role of miRNAs in chronic hepatitis B (CHB)-induced liver damage remains poorly understood. Here, we investigated the role of miRNAs in CHB-related liver damage. Microarray analysis of the expression of miRNAs in 22 CHB patients and 33 healthy individuals identified miR-194 as one of six differentially expressed miRNAs. miR-194 was up-regulated in correlation with increased liver damage in the plasma or liver tissues of CHB patients. In mice subjected to 2/3 partial hepatectomy, miR-194 was up-regulated in liver tissues in correlation with hepatocyte growth and in parallel with the down-regulation of the activin receptor ACVR2B. Overexpression of miR-194 in human liver HL7702 cells down-regulated ACVR2B mRNA and protein expression, promoted cell proliferation, acceleratedG1 to S cell cycle transition, and inhibited apoptosis, whereas knockdown of miR-194 had the opposite effects. Luciferase reporter assays confirmed that ACVR2B is a direct target of miR-194, and overexpression of ACVR2B significantly repressed cell proliferation and G1 to S phase transition and induced cell apoptosis. ACVR2B overexpression abolished the effect of miR-194, indicating that miR-194 promotes hepatocyte proliferation and inhibits apoptosis by down-regulating ACVR2B. Taken together, these results indicate that miR-194 plays a crucial role in hepatocyte proliferation and liver regeneration by targeting ACVR2B and may represent a novel therapeutic target for the treatment of CHB-related liver damage.

  • 推荐引用方式
    GB/T 7714:
    Gao Xue,Zhao Pan,Hu Jie, et al. MicroRNA-194 protects against chronic hepatitis B-related liver damage by promoting hepatocyte growth via ACVR2B [J].JOURNAL OF CELLULAR AND MOLECULAR MEDICINE,2018,22(9):4534-4544.
  • APA:
    Gao Xue,Zhao Pan,Hu Jie,Zhu Hongguang,&Tang Feng.(2018).MicroRNA-194 protects against chronic hepatitis B-related liver damage by promoting hepatocyte growth via ACVR2B .JOURNAL OF CELLULAR AND MOLECULAR MEDICINE,22(9):4534-4544.
  • MLA:
    Gao Xue, et al. "MicroRNA-194 protects against chronic hepatitis B-related liver damage by promoting hepatocyte growth via ACVR2B" .JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 22,9(2018):4534-4544.
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