MiR-148a promotes apoptosis by targeting Bcl-2 in colorectal cancer

被引:184
|
作者
Zhang, H. [1 ]
Li, Y. [1 ]
Huang, Q. [1 ]
Ren, X. [1 ]
Hu, H. [1 ]
Sheng, H. [1 ]
Lai, M. [1 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Pathol, Hangzhou 310058, Zhejiang, Peoples R China
来源
CELL DEATH AND DIFFERENTIATION | 2011年 / 18卷 / 11期
基金
中国国家自然科学基金;
关键词
colorectal cancer; miR-148a; apoptosis; Bcl-2; PREGNANE-X-RECEPTOR; GENE-EXPRESSION; CELL-DEATH; C-MYC; MICRORNAS; PROTEINS; FAMILY; P53; INHIBITION; TRIGGERS;
D O I
10.1038/cdd.2011.28
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis has a vital role in maintaining tissue homeostasis, and dysregulation of the apoptotic pathway is now widely recognized as a key step in tumourigenesis. Increasingly, evidence has demonstrated that microRNA (miRNA) can exert various biological functions in tumours by targeting oncogenes or tumour suppressors. Nevertheless, the role of miRNA in apoptosis remains unclear. Here we show that ectopical expression of miR-148a can induce apoptosis in colorectal cancer cells. In addition, MYB can inhibit miR-148a by directly acting on the transcription factor binding site in miR-148a gene and miR-148a can posttranscriptionally silence Bcl-2. Subsequently, the intrinsic apoptosis pathway is activated by releasing cytochrome c, cleaving caspase 9, caspase 3 and PARP, which eventually induce cancer-cell apoptosis. These findings are part of a hitherto undocumented apoptotic regulatory pathway in which a pleiotropic transcription factor controls the expression of a miRNA and the miRNA inhibits the target, leading to activation of an intrinsic mitochondrial pathway and tumour apoptosis. Cell Death and Differentiation (2011) 18, 1702-1710; doi: 10.1038/cdd.2011.28; published online 1 April 2011
引用
收藏
页码:1702 / 1710
页数:9
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