首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Ginsenoside Rh2 Induces Human Hepatoma Cell Apoptosis via Bax/Bak Triggered Cytochrome C Release and Caspase-9/Caspase-8 Activation
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Ginsenoside Rh2 Induces Human Hepatoma Cell Apoptosis via Bax/Bak Triggered Cytochrome C Release and Caspase-9/Caspase-8 Activation

机译:人参皂苷Rh2通过Bax / Bak触发的细胞色素C释放和Caspase-9 / Caspase-8激活诱导人肝癌细胞凋亡。

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摘要

Ginsenoside Rh2 (G-Rh2) has been shown to induce apoptotic cell death in a variety of cancer cells. However, the details of the signal transduction cascade involved in G-Rh2-induced cell death is unclear. In this manuscript we elucidate the molecular mechanism of G-Rh2-induced apoptosis in human hepatoma SK-HEP-1 cells by demonstrating that G-Rh2 causes rapid and dramatic translocation of both Bak and Bax, which subsequently triggers mitochondrial cytochrome c release and consequent caspase activation. Interestingly, siRNA-based gene inactivation of caspase-8 effectively delays caspase-9 activation and apoptosis induced by G-Rh2, indicating that caspase-8 also plays an important role in the G-Rh2-induced apoptosis program. Taken together, our results indicate that G-Rh2 employs a multi pro-apoptotic pathway to execute cancer cell death, suggesting a potential role for G-Rh2 as a powerful chemotherapeutic agent.
机译:人参皂苷Rh2(G-Rh2)已被证明在多种癌细胞中诱导凋亡性细胞死亡。但是,有关G-Rh2诱导的细胞死亡的信号转导级联反应的细节尚不清楚。在本手稿中,我们通过证明G-Rh2引起Bak和Bax迅速而剧烈的易位,进而触发线粒体细胞色素c释放,进而阐明了G-Rh2诱导的人肝癌SK-HEP-1细胞凋亡的分子机制。半胱天冬酶激活。有趣的是,基于siRNA的caspase-8基因失活有效地延迟了由G-Rh2诱导的caspase-9活化和凋亡,这表明caspase-8在G-Rh2诱导的凋亡程序中也起着重要作用。两者合计,我们的结果表明,G-Rh2采用多种促凋亡途径来执行癌细胞死亡,表明G-Rh2作为强大的化学治疗剂具有潜在的作用。

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