Liao Jun-Ming, Cao Bo, Zhou Xiang, Lu Hua
Department of Biochemistry & Molecular Biology and Tulane Cancer Center, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Department of Biochemistry & Molecular Biology and Tulane Cancer Center, Tulane University School of Medicine, New Orleans, LA 70112, USA
J Mol Cell Biol. 2014 Jun;6(3):206-13. doi: 10.1093/jmcb/mju018. Epub 2014 Apr 15.
The tumor suppressor p53 pathway, whose alterations are highly associated with all types of human cancers, plays an essential role in preventing tumor development and progression mostly through its downstream target genes. Over the last decade, a growing list of p53 microRNA (miRNA) targets has been identified as additional downstream players of this pathway. Further studies of these miRNAs have revealed their more complicated regulations and functions in executing and/or regulating p53 activity. Here, we review the p53 miRNA targets identified thus far, and discuss how they fine-tune p53 stress responses, mediate the crosstalk between p53 and other signaling pathways, and expand the role of p53 in other human diseases in addition to cancers.
肿瘤抑制因子p53通路的改变与所有类型的人类癌症高度相关,它主要通过其下游靶基因在预防肿瘤发生和发展中发挥重要作用。在过去十年中,越来越多的p53微小RNA(miRNA)靶标被鉴定为该通路的其他下游作用因子。对这些miRNA的进一步研究揭示了它们在执行和/或调节p53活性方面更复杂的调控和功能。在这里,我们回顾了迄今为止鉴定出的p53 miRNA靶标,并讨论它们如何微调p53应激反应、介导p53与其他信号通路之间的相互作用,以及扩展p53在除癌症之外的其他人类疾病中的作用。