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
[41]   MLL: a histone methyltransferase disrupted in leukemia [J].
Hess, JL .
TRENDS IN MOLECULAR MEDICINE, 2004, 10 (10) :500-507
[42]   De novo methylation and co-suppression induced by a cytoplasmically replicating plant RNA virus [J].
Jones, AL ;
Thomas, CL ;
Maule, AJ .
EMBO JOURNAL, 1998, 17 (21) :6385-6393
[43]   Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription [J].
Jones, PL ;
Veenstra, GJC ;
Wade, PA ;
Vermaak, D ;
Kass, SU ;
Landsberger, N ;
Strouboulis, J ;
Wolffe, AP .
NATURE GENETICS, 1998, 19 (02) :187-191
[44]   DNA METHYLATION AFFECTS THE FORMATION OF ACTIVE CHROMATIN [J].
KESHET, I ;
LIEMANHURWITZ, J ;
CEDAR, H .
CELL, 1986, 44 (04) :535-543
[45]   Chromatin immunoprecipitation microarrays for identification of genes silenced by histone H3 lysine 9 methylation [J].
Kondo, Y ;
Shen, L ;
Yan, PS ;
Huang, THM ;
Issa, JPJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) :7398-7403
[46]   Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins [J].
Lachner, M ;
O'Carroll, N ;
Rea, S ;
Mechtler, K ;
Jenuwein, T .
NATURE, 2001, 410 (6824) :116-120
[47]   PURIFICATION, SEQUENCE, AND CELLULAR-LOCALIZATION OF A NOVEL CHROMOSOMAL PROTEIN THAT BINDS TO METHYLATED DNA [J].
LEWIS, JD ;
MEEHAN, RR ;
HENZEL, WJ ;
MAURERFOGY, I ;
JEPPESEN, P ;
KLEIN, F ;
BIRD, A .
CELL, 1992, 69 (06) :905-914
[48]   Genetic unmasking of an epigenetically silenced microRNA in human cancer cells [J].
Lujambio, Amaia ;
Ropero, Santiago ;
Ballestar, Esteban ;
Fraga, Mario F. ;
Cerrato, Celia ;
Setien, Fernando ;
Casado, Sara ;
Suarez-Gauthier, Ana ;
Sanchez-Cespedes, Montserrat ;
Gitt, Anna ;
Spiteri, Inmaculada ;
Das, Partha P. ;
Caldas, Carlos ;
Miska, Eric ;
Esteller, Manel .
CANCER RESEARCH, 2007, 67 (04) :1424-1429
[49]   Selective association of the methyl-CpG binding protein MBD2 with the silent p14/p16 locus in human neoplasia [J].
Magdinier, F ;
Wolffe, AP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (09) :4990-4995
[50]   5-METHYLCYTOSINE LOCALIZED IN MAMMALIAN CONSTITUTIVE HETEROCHROMATIN [J].
MILLER, OJ ;
SCHNEDL, W ;
ALLEN, J ;
ERLANGER, BF .
NATURE, 1974, 251 (5476) :636-637