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SIRT6 过表达诱导癌细胞发生大量细胞凋亡,但不会诱导正常细胞发生凋亡。

SIRT6 overexpression induces massive apoptosis in cancer cells but not in normal cells.

机构信息

University of Rochester, Rochester, NY, USA.

出版信息

Cell Cycle. 2011 Sep 15;10(18):3153-8. doi: 10.4161/cc.10.18.17435.

Abstract

Emerging evidence suggests that Sirtuin 6 (SIRT6) functions as a longevity assurance gene by promoting genomic stability, regulating metabolic processes and attenuating inflammation. Here, we examine the effect of SIRT6 activation on cancer cells. We show that SIRT6 overexpression induces massive apoptosis in a variety of cancer cell lines but not in normal, non-transformed cells. This cell death requires the mono-ADP-ribosyltransferase but not the deacetylase activity of SIRT6 and is mediated by the activation of both the p53 and p73 apoptotic signaling cascades in cancer cells by SIRT6. These results suggest that SIRT6 is an attractive target for pharmacological activation in cancer treatment.

摘要

新出现的证据表明,Sirtuin 6(SIRT6)通过促进基因组稳定性、调节代谢过程和减轻炎症来发挥长寿保证基因的作用。在这里,我们研究了 SIRT6 激活对癌细胞的影响。我们表明,SIRT6 过表达在多种癌细胞系中诱导大量细胞凋亡,但在正常、未转化的细胞中则不会。这种细胞死亡需要 SIRT6 的单 ADP-核糖基转移酶而不是去乙酰化酶活性,并且由 SIRT6 在癌细胞中激活 p53 和 p73 凋亡信号级联来介导。这些结果表明,SIRT6 是癌症治疗中药物激活的有吸引力的靶标。

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