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p53通过诱导肿瘤抑制因子miR-145来抑制c-Myc。

p53 represses c-Myc through induction of the tumor suppressor miR-145.

作者信息

Sachdeva Mohit, Zhu Shoumin, Wu Fangting, Wu Hailong, Walia Vijay, Kumar Sumit, Elble Randolph, Watabe Kounosuke, Mo Yin-Yuan

机构信息

Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, IL 62794, USA.

出版信息

Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3207-12. doi: 10.1073/pnas.0808042106. Epub 2009 Feb 6.

Abstract

The tumor suppressor p53 negatively regulates a number of genes, including the proto-oncogene c-Myc, in addition to activating many other genes. One mechanism of the p53-mediated c-Myc repression may involve transcriptional regulation. However, it is not clear whether microRNAs (miRNAs) play a role in the p53-mediated posttranscriptional regulation of c-Myc. In this study, we show that a putative tumor suppressor, miR-145, is expressed through the phosphoinositide-3 kinase (PI-3K)/Akt and p53 pathways. Importantly, p53 transcriptionally induces the expression of miR-145 by interacting with a potential p53 response element (p53RE) in the miR-145 promoter. We further show that c-Myc is a direct target for miR-145. Although miR-145 silences the expression of c-Myc, anti-miR-145 enhances its expression. This specific silencing of c-Myc by miR-145 accounts at least in part for the miR-145-mediated inhibition of tumor cell growth both in vitro and in vivo. Finally, the blockade of miR-145 by anti-miR-145 is able to reverse the p53-mediated c-Myc repression. Together, these results define the role of miR-145 in the posttranscriptional regulation of c-Myc by p53 and suggest that, as a new member of the p53 regulatory network, miR-145 provides a direct link between p53 and c-Myc in this gene regulatory network.

摘要

肿瘤抑制因子p53除了激活许多其他基因外,还对包括原癌基因c-Myc在内的一些基因进行负调控。p53介导的c-Myc抑制的一种机制可能涉及转录调控。然而,尚不清楚微小RNA(miRNA)是否在p53介导的c-Myc转录后调控中发挥作用。在本研究中,我们表明一种假定的肿瘤抑制因子miR-145通过磷酸肌醇-3激酶(PI-3K)/Akt和p53途径表达。重要的是,p53通过与miR-145启动子中的潜在p53反应元件(p53RE)相互作用转录诱导miR-145的表达。我们进一步表明c-Myc是miR-145的直接靶标。虽然miR-145使c-Myc的表达沉默,但抗miR-145增强其表达。miR-145对c-Myc的这种特异性沉默至少部分解释了miR-145在体外和体内介导的肿瘤细胞生长抑制。最后,抗miR-145对miR-145的阻断能够逆转p53介导的c-Myc抑制。总之,这些结果确定了miR-145在p53对c-Myc的转录后调控中的作用,并表明,作为p53调控网络的新成员,miR-145在这个基因调控网络中提供了p53和c-Myc之间的直接联系。

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