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Bax 抑制剂-1(BI-1)过表达诱导 NIH3T3 细胞发生转化。

Overexpression of Bax inhibitor-1 (BI-1) induces cell transformation in NIH3T3 cells.

机构信息

Center of Clinical Gene Diagnosis, Zhongnan Hospital of Wuhan University, Hubei, China.

出版信息

Cell Biol Int. 2010 Nov;34(11):1099-104. doi: 10.1042/CBI20090400.

Abstract

BI-1 (Bax inhibitor-1), an apoptosis-inhibiting gene belonging to the Bcl-2 protein family, plays an important role in mitochondrial apoptosis pathway to suppress Bax-induced apoptosis. To investigate the potential role of BI-1 in promoting cell growth and tumorigenesis, in the present study we overexpressed the BI-1 gene in NIH3T3 cells using the lentivirus-mediated gene expression system. Our in vitro studies showed that NIH3T3 cells overexpressing BI-1 displayed a significantly higher growth rate and formed more and larger colonies than the control cells. In addition, our in vivo studies indicated that the lenti-BI-1-infected cells formed obvious tumours, while no tumours were formed by the control cells after subcutaneously injected into nude mice. These results strongly suggested that the BI-1 gene might play a crucial role in neoplastic genesis and development.

摘要

BI-1(Bax 抑制剂-1)是 Bcl-2 蛋白家族中的凋亡抑制基因,在调控线粒体凋亡途径中发挥重要作用,抑制 Bax 诱导的细胞凋亡。为了研究 BI-1 促进细胞生长和肿瘤发生的潜在作用,本研究通过慢病毒介导的基因表达系统在 NIH3T3 细胞中过表达 BI-1 基因。体外研究结果表明,过表达 BI-1 的 NIH3T3 细胞的生长速度明显高于对照组,形成的集落更多、更大。此外,体内研究表明,慢病毒感染 BI-1 的细胞形成了明显的肿瘤,而对照组细胞接种到裸鼠后则未形成肿瘤。这些结果强烈提示 BI-1 基因可能在肿瘤的发生和发展中起关键作用。

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