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抑制素通过线粒体途径诱导BGC823胃癌细胞凋亡。

Prohibitin induces apoptosis in BGC823 gastric cancer cells through the mitochondrial pathway.

作者信息

Zhang Long, Ji Qing, Ni Zhen-Hua, Sun Jian

机构信息

Interventional Oncology Institute of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Asian Pac J Cancer Prev. 2012;13(8):3803-7. doi: 10.7314/apjcp.2012.13.8.3803.

Abstract

Prohibitin (PHB), an evolutionarily-conserved protein, has been found to be over-expressed in gastric cancer and be closely related with tumor malignancy. In this study, to investigate the relationship between PHB expression and cell apoptosis in the BGC823 gastric cancer cell line, low and high expression PHB in BGC823 cells was accomplished using RNA interference technology and gene transfer techniques. Cell proliferation, cell cycling, apoptosis, Bax, Bcl-2 and Cyt.c protein expression and the activation of Caspase-3,9 were assessed after 48 h. Over-expression of PHB gene in BGC823 cells resulted in slow cell growth, cell arrest in G2 phase, and an increased apoptosis ratio while the opposite was found for PHB under-expressing cells. In PHB over-expressing cells, the expression of Bax gene was increased, the expression of Bcl-2 was decreased, the activation level of Caspase-3, 9 was increased, but the activation level of Caspase-8 demonstrated no change. These results indicate that PHB induced apoptosis through the mitochondrial pathway.

摘要

抑制素(PHB)是一种进化上保守的蛋白质,已发现在胃癌中过度表达,且与肿瘤恶性程度密切相关。在本研究中,为了探讨BGC823胃癌细胞系中PHB表达与细胞凋亡之间的关系,利用RNA干扰技术和基因转移技术实现了BGC823细胞中PHB的低表达和高表达。48小时后评估细胞增殖、细胞周期、凋亡、Bax、Bcl-2和细胞色素c蛋白表达以及Caspase-3、9的激活情况。BGC823细胞中PHB基因的过表达导致细胞生长缓慢、细胞停滞在G2期以及凋亡率增加,而PHB低表达细胞则出现相反情况。在PHB过表达细胞中,Bax基因表达增加,Bcl-2表达降低,Caspase-3、9的激活水平增加,但Caspase-8的激活水平无变化。这些结果表明,PHB通过线粒体途径诱导细胞凋亡。

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