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

被引:710
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
相关论文
共 30 条
[1]   Histone modifications and silencing prior to DNA methylation of a tumor suppressor gene [J].
Bachman, KE ;
Park, BH ;
Rhee, I ;
Rajagopalan, H ;
Herman, JG ;
Baylin, SB ;
Kinzler, KW ;
Vogelstein, B .
CANCER CELL, 2003, 3 (01) :89-95
[2]   Basic fibroblast growth factor and ultraviolet B transform melanocytes in human skin [J].
Berking, C ;
Takemoto, R ;
Satyamoorthy, K ;
Elenitsas, R ;
Herlyn, M .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (03) :943-953
[3]   p53-mediated activation of miRNA34 candidate tumor-suppressor genes [J].
Bommer, Guido T. ;
Gerin, Isabelle ;
Feng, Ying ;
Kaczorowski, Andrew J. ;
Kuick, Rork ;
Love, Robert E. ;
Zhai, Yali ;
Giordano, Thomas J. ;
Qin, Zhaohui S. ;
Moore, Bethany B. ;
MacDougald, Ormond A. ;
Cho, Kathleen R. ;
Fearon, Eric R. .
CURRENT BIOLOGY, 2007, 17 (15) :1298-1307
[4]   MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866
[5]   A functional study of miR-124 in the developing neural tube [J].
Cao, Xinwei ;
Pfaff, Samuel L. ;
Gage, Fred H. .
GENES & DEVELOPMENT, 2007, 21 (05) :531-536
[6]   Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis [J].
Chang, Tsung-Cheng ;
Wentzel, Erik A. ;
Kent, Oliver A. ;
Ramachandran, Kalyani ;
Mullendore, Michael ;
Lee, Kwang Hyuck ;
Feldmann, Georg ;
Yamakuchi, Munekazu ;
Ferlito, Marcella ;
Lowenstein, Charles J. ;
Arking, Dan E. ;
Beer, Michael A. ;
Maitra, Anirban ;
Mendell, Joshua T. .
MOLECULAR CELL, 2007, 26 (05) :745-752
[7]   A functional screen identifies miR-34a as a candidate neuroblastoma tumor suppressor gene [J].
Cole, Kristina A. ;
Attiyeh, Edward F. ;
Mosse, Yael P. ;
Laquaglia, Michael J. ;
Diskin, Sharon J. ;
Brodeur, Garrett M. ;
Maris, John M. .
MOLECULAR CANCER RESEARCH, 2008, 6 (05) :735-742
[8]   Interfering with disease: a progress report on siRNA-based therapeutics [J].
de Fougerolles, Antonin ;
Vornlocher, Hans-Peter ;
Maraganore, John ;
Lieberman, Judy .
NATURE REVIEWS DRUG DISCOVERY, 2007, 6 (06) :443-453
[9]   Inducible microRNA expression by an all-in-one episomal vector system [J].
Epanchintsev, Alexey ;
Jung, Peter ;
Menssen, Antje ;
Hermeking, Heiko .
NUCLEIC ACIDS RESEARCH, 2006, 34 (18)
[10]   Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? [J].
Filipowicz, Witold ;
Bhattacharyya, Suvendra N. ;
Sonenberg, Nahum .
NATURE REVIEWS GENETICS, 2008, 9 (02) :102-114