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短发夹 RNA 抑制 MED19 表达可诱导人前列腺癌细胞增殖和致瘤性抑制。

Suppression of MED19 expression by shRNA induces inhibition of cell proliferation and tumorigenesis in human prostate cancer cells.

机构信息

Urology Department of Surgery, Changzheng Hospital Affiliated to the Second Military Medical University, Shanghai, People's Republic of China.

出版信息

BMB Rep. 2011 Aug;44(8):547-52. doi: 10.5483/bmbrep.2011.44.8.547.

Abstract

MED19 is a member of the Mediator that plays a key role in the activation and repression of signal transduction or the regulation of transcription in carcinomas. To tested the functional role of MED19 in human prostate cancer, we downregulated MED19 expression in prostate cancer cells (PC-3 and DU145) by lentivirus-mediated short hairpin (shRNA), and analyzed the effect of inhibition of MED19 on prostate cancer cell proliferation and tumorigenesis. The in vitro prostate cancer cell proliferation, colony formation, and in vivo tumor growth in nude mice xenografts was significantly reduced after the downregulation of MED19. Knockdown of MED19 caused S-phase arrest and induced apoptosis via modulation of Bid and Caspase 7. It was suggested that MED19 serves as a novel proliferation regulator that promotes growth of prostate cancer cells.

摘要

MED19 是 Mediator 的一个成员,在信号转导的激活和抑制或转录的调节中发挥关键作用,在癌中。为了测试 MED19 在人类前列腺癌中的功能作用,我们通过慢病毒介导的短发夹 (shRNA) 下调前列腺癌细胞 (PC-3 和 DU145) 中的 MED19 表达,并分析抑制 MED19 对前列腺癌细胞增殖和肿瘤发生的影响。下调 MED19 后,体外前列腺癌细胞增殖、集落形成和体内裸鼠异种移植肿瘤生长明显减少。MED19 的敲低导致 S 期停滞,并通过调节 Bid 和 Caspase 7 诱导细胞凋亡。提示 MED19 作为一种新型的增殖调节剂,促进前列腺癌细胞的生长。

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