Epigenetics at the epicenter of modern medicine

被引:259
作者
Feinberg, Andrew P. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Ctr Epigenet, Baltimore, MD 21205 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2008年 / 299卷 / 11期
关键词
D O I
10.1001/jama.299.11.1345
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epigenetics, the study of non- DNA sequence- related heredity, is at the epicenter of modern medicine because it can help to explain the relationship between an individual's genetic background, the environment, aging, and disease. It can do so because the epigenetic state varies among tissues and during a lifetime, whereas the DNA sequence remains essentially the same. As cells adapt to a changing internal and external environment, epigenetic mechanisms can remember these changes in the normal programming and reprogramming of gene activity. The common disease genetic and epigenetic ( CDGE) model provides an epidemiologic framework that can incorporate epigenetic with genetic variation in the context of age- related susceptibility to disease. Under CDGE, the epigenetic program can modify the effects of deleterious genes or may be influenced by an adverse environment. Thus, including epigenetics into epidemiologic studies of human disease may help explain the relationship between the genome and the environment and may provide new clues to modifying these effects in disease prevention and therapy.
引用
收藏
页码:1345 / 1350
页数:6
相关论文
共 40 条
[1]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[2]   The complex language of chromatin regulation during transcription [J].
Berger, Shelley L. .
NATURE, 2007, 447 (7143) :407-412
[3]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326
[4]   An integrated epigenetic and genetic approach to common human disease [J].
Bjornsson, HT ;
Fallin, MD ;
Feinberg, AP .
TRENDS IN GENETICS, 2004, 20 (08) :350-358
[5]   SATB1 packages densely looped, transcriptionally active chromatin for coordinated expression of cytokine genes [J].
Cai, Shutao ;
Lee, Charles C. ;
Kohwi-Shigematsu, Terumi .
NATURE GENETICS, 2006, 38 (11) :1278-1288
[6]   Loss of IGF2 imprinting:: A potential marker of colorectal cancer risk [J].
Cui, HM ;
Cruz-Correa, M ;
Giardiello, FM ;
Hutcheon, DF ;
Kafonek, DR ;
Brandenburg, S ;
Wu, YQ ;
He, XB ;
Powe, NR ;
Feinberg, AP .
SCIENCE, 2003, 299 (5613) :1753-1755
[7]   Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects [J].
DeBaun, MR ;
Niemitz, EL ;
McNeil, DE ;
Brandenburg, SA ;
Lee, MP ;
Feinberg, AP .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (03) :604-611
[8]   DNA methylation profiling of human chromosomes 6, 20 and 22 [J].
Eckhardt, Florian ;
Lewin, Joern ;
Cortese, Rene ;
Rakyan, Vardhman K. ;
Attwood, John ;
Burger, Matthias ;
Burton, John ;
Cox, Tony V. ;
Davies, Rob ;
Down, Thomas A. ;
Haefliger, Carolina ;
Horton, Roger ;
Howe, Kevin ;
Jackson, David K. ;
Kunde, Jan ;
Koenig, Christoph ;
Liddle, Jennifer ;
Niblett, David ;
Otto, Thomas ;
Pettett, Roger ;
Seemann, Stefanie ;
Thompson, Christian ;
West, Tony ;
Rogers, Jane ;
Olek, Alex ;
Berlin, Kurt ;
Beck, Stephan .
NATURE GENETICS, 2006, 38 (12) :1378-1385
[9]   Phenotypic plasticity and the epigenetics of human disease [J].
Feinberg, Andrew P. .
NATURE, 2007, 447 (7143) :433-440
[10]   HYPOMETHYLATION DISTINGUISHES GENES OF SOME HUMAN CANCERS FROM THEIR NORMAL COUNTERPARTS [J].
FEINBERG, AP ;
VOGELSTEIN, B .
NATURE, 1983, 301 (5895) :89-92