MiR-34, SIRT1 and p53 The feedback loop

被引:380
作者
Yamakuchi, Munekazu [1 ]
Lowenstein, Charles J. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
关键词
microRNA (miRNA); p53; miR-34; apoptosis; SIRT1; TUMOR-SUPPRESSOR; MICRORNA EXPRESSION; CELL-SURVIVAL; SACCHAROMYCES-CEREVISIAE; INCREASED DOSAGE; LIFE-SPAN; CANCER; TRANSCRIPTION; APOPTOSIS; TRANSFORMATION;
D O I
10.4161/cc.8.5.7753
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression. Several studies have linked dysregulation of miRNA with tumorigenesis. The TP53 is one of the most commonly mutated genes in human cancers, and its gene product p53 activates transcription of a set of miRNA including the miR-34 family of miRNA. The miR-34 family regulates cell cycle progression, cellular senescence and apoptosis, but the targets of miR-34 are not completely defined. We recently found that miR-34a inhibits SIRT1, a gene that regulates cellular senescence and limits longevity. SIRT1 also regulates p53 dependent apoptosis through deacetylating and stabilizing p53. We also discovered that SIRT1 mediates miR-34a activation of apoptosis by regulating p53 activity. Based on this observation, we propose a positive feedback loop, in which p53 induces expression of miR-34a which suppresses SIRT1, increasing p53 activity.
引用
收藏
页码:712 / 715
页数:4
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