microRNAs join the p53 network - another piece in the tumour-suppression puzzle

被引:439
作者
He, Lin
He, Xingyue
Lowe, Scott W.
Hannon, Gregory J.
机构
[1] Cold Spring Harbor Lab, Howard Hughes Med Inst, Watson Sch Biol Sci, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Genet Program, Stony Brook, NY 11794 USA
关键词
D O I
10.1038/nrc2232
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several recent studies have found a conserved microRNA (miRNA) family, the miR-34s, to be direct transcriptional targets of p53. miR-34 activation can recapitulate elements of p53 activity, including induction of cell-cycle arrest and promotion of apoptosis, and loss of miR-34 can impair p53-mediated cell death. These data reinforce the growing awareness that non-coding RNAs are key players in tumour development by placing miRNAs in a central role in a well-known tumour-suppressor network.
引用
收藏
页码:819 / 822
页数:4
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