Epigenetic Gene Regulation in Cancer

被引:58
作者
Ballestar, Esteban [1 ]
Esteller, Manel [1 ]
机构
[1] Spanish Natl Canc Ctr CNIO, Mol Pathol Programme, Canc Epigenet Grp, Madrid 28029, Spain
来源
LONG-RANGE CONTROL OF GENE EXPRESSION | 2008年 / 61卷
关键词
D O I
10.1016/S0065-2660(07)00009-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The observation that cancer cells suffer profound alterations in the DNA methylation profile, with functional consequences in the activity of key genes, together with the recognition that epigenetic alterations might be as important as genetic defects in the origin of cancers has started a new era in cancer research. In a few years, key discoveries have abruptly changed our vision of the determinants of cancer. Breakthroughs in the cancer epigenetics field include the finding of a tumor-type specificity of genes that suffer epigenetic deregulation at both DNA methylation and histone modifications, the interconnection between different epigenetic marks, the identification of mechanisms of targeting of epigenetic alterations, including the participation of Polycomb group (PcG) proteins, or the involvement of small RNAs, which regulate hundreds of target genes. All these findings have multiple implications: first, they shed light on the mechanistic insights by which epigenetic defects complement genetic alterations in the development and progression of cancer; second, epigenetic alterations appear to play a prominent role in the initiation of cancer. In addition, because epigenetic changes are reversible, enzymes involved in their maintenance stand as targets for a variety of compounds for therapy. (C) 2008, Elsevier Inc.
引用
收藏
页码:247 / 267
页数:21
相关论文
共 83 条
[21]  
Esteller M, 2001, CANCER RES, V61, P3225
[22]   hMLH1 promoter hypermethylation is an early event in human endometrial tumorigenesis [J].
Esteller, M ;
Catasus, L ;
Matias-Guiu, X ;
Mutter, GL ;
Prat, J ;
Baylin, SB ;
Herman, JG .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (05) :1767-1772
[23]  
Esteller M, 2000, CANCER RES, V60, P2368
[24]   HYPOMETHYLATION DISTINGUISHES GENES OF SOME HUMAN CANCERS FROM THEIR NORMAL COUNTERPARTS [J].
FEINBERG, AP ;
VOGELSTEIN, B .
NATURE, 1983, 301 (5895) :89-92
[25]   A family of human zinc finger proteins that bind methylated DNA and repress transcription [J].
Filion, GJP ;
Zhenilo, S ;
Salozhin, S ;
Yamada, D ;
Prokhortchouk, E ;
Defossez, PA .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (01) :169-181
[26]   Cellular identity and lineage choice [J].
Fisher, AG .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (12) :977-982
[27]  
Fleisher AS, 1999, CANCER RES, V59, P1090
[28]   Hypermethylation of the hMLH1 gene promoter is associated with microsatellite instability in early human gastric neoplasia [J].
Fleisher, AS ;
Esteller, M ;
Tamura, G ;
Rashid, A ;
Stine, OC ;
Yin, J ;
Zou, TT ;
Abraham, JM ;
Kong, DH ;
Nishizuka, S ;
James, SP ;
Wilson, KT ;
Herman, JG ;
Meltzer, SJ .
ONCOGENE, 2001, 20 (03) :329-335
[29]   Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer [J].
Fraga, MF ;
Ballestar, E ;
Villar-Garea, A ;
Boix-Chornet, M ;
Espada, J ;
Schotta, G ;
Bonaldi, T ;
Haydon, C ;
Ropero, S ;
Petrie, K ;
Iyer, NG ;
Pérez-Rosado, A ;
Calvo, E ;
Lopez, JA ;
Cano, A ;
Calasanz, MJ ;
Colomer, D ;
Piris, MA ;
Ahn, N ;
Imhof, A ;
Caldas, C ;
Jenuwein, T ;
Esteller, M .
NATURE GENETICS, 2005, 37 (04) :391-400
[30]   Dnmt3a binds deacetylases and is recruited by a sequence-specific repressor to silence transcription [J].
Fuks, F ;
Burgers, WA ;
Godin, N ;
Kasai, M ;
Kouzarides, T .
EMBO JOURNAL, 2001, 20 (10) :2536-2544