Epigenetics: The role of methylation in the mechanism of action of tumor suppressor genes

被引:34
作者
Jain, PK [1 ]
机构
[1] US FDA, DETTD, OBRR, CBER, Rockville, MD 20852 USA
来源
EPIGENETICS IN CANCER PREVENTION: EARLY DETECTION AND RISK ASSESSMENT | 2003年 / 983卷
关键词
epigenetics; hypermethylation; tumor suppressor genes; histone deacetylase (HDAC); histone methylase (HMT);
D O I
10.1111/j.1749-6632.2003.tb05963.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetics is the study of mitotically heritable changes in gene expression without any changes in the primary DNA sequence. The major step in epigenetic gene regulation is gene inactivation by hypermethylation of CpG islands located in the promoter region. Specific enzymes and methylated DNA binding proteins play a major role in causing reduced expression of tumor suppressor genes, resulting in tumor formation and its progression. Prevention approaches are needed to avoid tumor formation. One approach to inhibiting inactivation of tumor suppressor genes is to use chemical agents such as 5-azacytidine to prevent hypermethylation of DNA. Increased understanding of the mechanism of epigenetic silencing and the identification of additional molecular mechanisms (e.g., histone methylases) that may be targeted by pharmaceutical interventions may lead to more preventive strategies. The current status of the epigenetic regulation of tumor suppressor genes is discussed in this review article.
引用
收藏
页码:71 / 83
页数:13
相关论文
共 81 条
[71]   Epigenetic gene silencing in cancer [J].
Tycko, B .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (04) :401-407
[72]   The "dark side" of chromatin remodeling: Repressive effects on transcription [J].
Tyler, JK ;
Kadonaga, JT .
CELL, 1999, 99 (05) :443-446
[73]   Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation [J].
Wade, PA ;
Gegonne, A ;
Jones, PL ;
Ballestar, E ;
Aubry, F ;
Wolffe, AP .
NATURE GENETICS, 1999, 23 (01) :62-66
[74]   Phospholipase A2 and cyclooxygenase gene expression in human preimplantation embryos [J].
Wang, HB ;
Wen, Y ;
Mooney, S ;
Behr, B ;
Polan, ML .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (06) :2629-2634
[75]   Hypermethylation of the p15INK4b and P16INK4a in agnogenic myeloid metaplasia (AMM) and AMM in leukaemic transformation [J].
Wang, JC ;
Chen, W ;
Nallusamy, S ;
Chen, C ;
Novetsky, AD .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 116 (03) :582-586
[76]   Oligodendroglial tumors frequently demonstrate hypermethylation of the CDKN2A (MTS1, p16INK4a), p14ARF, and CDKN2B (MTS2, p15INK4b) tumor suppressor genes [J].
Wolter, M ;
Reifenberger, J ;
Blaschke, B ;
Ichimura, K ;
Schmidt, EE ;
Collins, VP ;
Reifenberger, G .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2001, 60 (12) :1170-1180
[77]   Cloning, expression and chromosome locations of the human DNMT3 gene family [J].
Xie, SP ;
Wang, ZJ ;
Okano, M ;
Nogami, M ;
Li, Y ;
He, WW ;
Okumura, K ;
Li, E .
GENE, 1999, 236 (01) :87-95
[78]  
YANG AS, 1996, EPIGENETIC MECH GENE, P77
[79]  
YEVIN A, 1993, DNA METHYLATION MOL, P523
[80]   A candidate mammalian DNA methyltransferase related to pmt1p of fission yeast [J].
Yoder, JA ;
Bestor, TH .
HUMAN MOLECULAR GENETICS, 1998, 7 (02) :279-284