Inactivation of miR-34a by aberrant CpG methylation in multiple types of cancer

被引:703
作者
Lodygin, Dmitri [2 ]
Tarasov, Valery [2 ]
Epanchintsev, Alexey [2 ]
Berking, Carola [3 ]
Knyazeva, Tatjana [4 ]
Koerner, Henrike [2 ]
Knyazev, Piotr [4 ]
Diebold, Joachim [5 ]
Hermeking, Heiko [1 ,2 ]
机构
[1] Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Univ Munich, Dept Dermatol, D-8000 Munich, Germany
[4] Max Planck Inst Biochem, Dept Mol Biol, D-82152 Martinsried, Germany
[5] Kantonsspital Luzern, Inst Pathol, Luzern, Switzerland
关键词
p53; miR-34a; tumor suppression; CpG methylation; carcinoma; melanoma; CDK6;
D O I
10.4161/cc.7.16.6533
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recently, we and others identified the microRNA miR-34a as a target of the tumor suppressor gene product p53. Ectopic miR-34a induces a G(1) cell cycle arrest, senescence and apoptosis. Here we report that miR-34a expression is silenced in several types of cancer due to aberrant CpG methylation of its promoter. 19 out of 24 (79.1%) primary prostate carcinomas displayed CpG methylation of the miR-34a promoter and concomitant loss of miR-34a expression. CpG methylation of the miR-34a promoter was also detected in breast (6/24; 25%), lung (7/24; 29.1%), colon (3/23; 13%), kidney (3/14; 21.4%), bladder (2/6; 33.3%) and pancreatic (3/19; 15.7%) carcinoma cell lines, as well as in melanoma cell lines (19/44; 43.2%) and primary melanoma (20/32 samples; 62.5%). Silencing of miR-34a was dominant over its transactivation by p53 after DNA damage. Re-expression of miR-34a in prostate and pancreas carcinoma cell lines induced senescence and cell cycle arrest at least in part by targeting CDK6. These results show that miR-34a represents a tumor suppressor gene which is inactivated by CpG methylation and subsequent transcriptional silencing in a broad range of tumors.
引用
收藏
页码:2591 / 2600
页数:10
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