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肿瘤抑制因子 p53 受 microRNA miR-504 的负调控。

Negative regulation of tumor suppressor p53 by microRNA miR-504.

机构信息

Cancer Institute of New Jersey, University of Medicine and Dentistry of New Jersey, New Brunswick, NJ 08903, USA.

出版信息

Mol Cell. 2010 Jun 11;38(5):689-99. doi: 10.1016/j.molcel.2010.05.027.

Abstract

Tumor suppressor p53 plays a central role in tumor prevention. p53 protein levels and activity are under a tight and complex regulation in cells to maintain the proper function of p53. MicroRNAs play a key role in the regulation of gene expression. Here we report the regulation of p53 through miR-504. miR-504 acts as a negative regulator of human p53 through its direct binding to two sites in the p53 3' untranslated region. Overexpression of miR-504 decreases p53 protein levels and functions in cells, including p53 transcriptional activity, p53-mediated apoptosis, and cell-cycle arrest in response to stress, and furthermore promotes tumorigenecity of cells in vivo. These results demonstrate the direct negative regulation of p53 by miR-504 as a mechanism for p53 regulation in cells, which highlights the importance of microRNAs in tumorigenesis.

摘要

抑癌基因 p53 在肿瘤预防中发挥着核心作用。p53 蛋白水平和活性在细胞中受到严格而复杂的调控,以维持 p53 的正常功能。microRNAs 在基因表达调控中发挥着关键作用。本文报道了 miR-504 通过直接结合 p53 3'UTR 的两个位点来调控 p53。miR-504 作为人 p53 的负调控因子,通过其直接结合 p53 3'UTR 的两个位点来发挥作用。miR-504 的过表达降低了细胞中 p53 蛋白水平和功能,包括 p53 转录活性、p53 介导的细胞凋亡以及应激诱导的细胞周期阻滞,并且进一步促进了细胞在体内的致瘤性。这些结果表明 miR-504 通过直接负调控 p53 作为细胞中 p53 调控的一种机制,突出了 microRNAs 在肿瘤发生中的重要性。

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