...
首页> 外文期刊>Virus Genes >Regulation of HepG2 cell apoptosis by hepatitis C virus (HCV) core protein via the sirt1-p53-bax pathway
【24h】

Regulation of HepG2 cell apoptosis by hepatitis C virus (HCV) core protein via the sirt1-p53-bax pathway

机译:丙型肝炎病毒(HCV)核心蛋白通过sirt1-p53-bax途径调控HepG2细胞凋亡

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Hepatitis C virus (HCV) core protein stimulates many signaling pathways related to apoptosis inhibition resulting in hepatocellular carcinoma (HCC). It has been reported that sirt1 is involved in regulating apoptosis; therefore, we investigated the influence of HCV core protein on sirt1 expression and apoptosis in human HepG2 cells. Our study showed that HCV core protein inhibited apoptosis of HepG2 cells as well as caspase-3 expression and activity (P < 0.05). At the same time, sirt1 expression was increased at both the mRNA (P < 0.05) and protein (P < 0.05) levels. Furthermore, apoptosis inhibition was reversed when sirt1 was knocked down (P < 0.05). Our study provides further evidence that the sirt1-p53-Bax signaling pathway plays an important role in regulating the suppression of cell apoptosis induced by HCV core protein.
机译:丙型肝炎病毒(HCV)核心蛋白刺激许多与凋亡抑制相关的信号通路,从而导致肝细胞癌(HCC)。据报道,sirt1参与调节细胞凋亡。因此,我们研究了HCV核心蛋白对人HepG2细胞中sirt1表达和凋亡的影响。我们的研究表明,HCV核心蛋白抑制HepG2细胞的凋亡以及caspase-3的表达和活性(P <0.05)。同时,sirt1表达在mRNA(P <0.05)和蛋白质(P <0.05)水平上均增加。此外,当sirt1被敲低时,细胞凋亡的抑制作用被逆转(P <0.05)。我们的研究提供了进一步的证据,表明sirt1-p53-Bax信号通路在调节HCV核心蛋白诱导的细胞凋亡的抑制中起着重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号