共 30 条
Inactivation of miR-34a by aberrant CpG methylation in multiple types of cancer
被引:710
作者:

Lodygin, Dmitri
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机构:
Max Planck Inst Biochem, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Tarasov, Valery
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机构:
Max Planck Inst Biochem, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Epanchintsev, Alexey
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h-index: 0
机构:
Max Planck Inst Biochem, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Berking, Carola
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h-index: 0
机构:
Univ Munich, Dept Dermatol, D-8000 Munich, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Knyazeva, Tatjana
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h-index: 0
机构:
Max Planck Inst Biochem, Dept Mol Biol, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Koerner, Henrike
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h-index: 0
机构:
Max Planck Inst Biochem, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Knyazev, Piotr
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h-index: 0
机构:
Max Planck Inst Biochem, Dept Mol Biol, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Diebold, Joachim
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h-index: 0
机构:
Kantonsspital Luzern, Inst Pathol, Luzern, Switzerland Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany

Hermeking, Heiko
论文数: 0 引用数: 0
h-index: 0
机构:
Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany
Max Planck Inst Biochem, D-82152 Martinsried, Germany Ruhr Univ Bochum, Inst Pathol, D-44789 Bochum, Germany
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
来源:
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.
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收藏
页码:2591 / 2600
页数:10
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