Zhang Cen, Liu Juan, Wang Xiaolong, Feng Zhaohui
Department of Radiation Oncology, Rutgers Cancer Institute of New Jersey, Rutgers, State University of New Jersey, New Brunswick, NJ 08903, USA.
RNA Dis. 2015;2(1):e502. doi: 10.14800/rd.502.
Tumor suppressor p53 and its signaling pathway play a central role in tumor prevention. The E3 ubiquitin ligase MDM2, which is a direct p53 transcriptional target and also the most critical negative regulator of p53, forms an autoregulatory negative feedback loop with p53 in the cell to tightly regulate the levels and activity of p53. MicroRNAs (miRNAs) are endogenously expressed small non-coding RNAs that play a critical role in the post-translational regulation of gene expression. Recent studies have revealed that miRNAs directly regulate the levels of p53 or MDM2 to modulate the p53 function in tumor suppression. Recently, we identified miR-339-5p as a new miRNA that directly represses MDM2 to activate p53 and enhance p53 function in tumor suppression. Thus, miRNAs have become a new but important component of the p53 signaling pathway through regulating the p53/MDM2 feedback loop.
肿瘤抑制因子p53及其信号通路在肿瘤预防中发挥着核心作用。E3泛素连接酶MDM2是p53的直接转录靶点,也是p53最关键的负调节因子,它在细胞内与p53形成一个自动调节的负反馈环,以严格调控p53的水平和活性。微小RNA(miRNA)是内源性表达的小非编码RNA,在基因表达的翻译后调控中起关键作用。最近的研究表明,miRNA直接调节p53或MDM2的水平,以调节p53在肿瘤抑制中的功能。最近,我们鉴定出miR-339-5p是一种新的miRNA,它直接抑制MDM2以激活p53并增强p53在肿瘤抑制中的功能。因此,miRNA通过调节p53/MDM2反馈环已成为p53信号通路一个新的但重要的组成部分。