The Second Hospital of Lanzhou University, Lanzhou 730030, Gansu, China.
Biochem Biophys Res Commun. 2012 Mar 23;419(4):656-61. doi: 10.1016/j.bbrc.2012.02.069. Epub 2012 Feb 21.
Hepatocellular carcinoma (HCC) is one of the most common internal malignant tumors. Glypican-3 (GPC3) is involved in the biological and molecular events in the tumorigenesis of HCC. We used RNA interference to evaluate the molecular effects of GPC3 suppression at the translational level and demonstrated for the first time that GPC3 silencing results in a significant elevation of the Bax/Bcl-2 ratio, the release of cytochrome c from mitochondria and the activation of caspase-3. The results suggest that GPC3 regulates cell proliferation by enhancing the resistance to apoptosis through the dysfunction of the Bax/Bcl-2/cytochrome c/caspase-3 signaling pathway and therefore plays a critical role in the tumorigenesis of HCC. Thus, the knockdown of GPC3 should be further investigated as an attractive novel approach for the targeted gene therapy of HCC.
肝细胞癌 (HCC) 是最常见的内脏恶性肿瘤之一。磷脂酰聚糖-3 (GPC3) 参与 HCC 肿瘤发生的生物学和分子事件。我们使用 RNA 干扰来评估 GPC3 抑制在翻译水平上的分子效应,并首次证明 GPC3 沉默导致 Bax/Bcl-2 比率显著升高、线粒体细胞色素 c 释放和 caspase-3 激活。结果表明,GPC3 通过增强抗细胞凋亡能力来调节细胞增殖,从而通过 Bax/Bcl-2/细胞色素 c/caspase-3 信号通路的功能障碍发挥关键作用在 HCC 的发生中。因此,敲低 GPC3 应该作为 HCC 靶向基因治疗的一种有吸引力的新方法进一步研究。