DNA甲基化
表观遗传学
癌变
甲基化
癌症
生物
癌症研究
DNA
癌症表观遗传学
遗传学
基因
基因表达
作者
Michael Klutstein,Deborah Nejman,Razi Greenfield,Howard Cedar
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2016-06-03
卷期号:76 (12): 3446-3450
被引量:735
标识
DOI:10.1158/0008-5472.can-15-3278
摘要
Abstract DNA methylation is known to be abnormal in all forms of cancer, but it is not really understood how this occurs and what is its role in tumorigenesis. In this review, we take a wide view of this problem by analyzing the strategies involved in setting up normal DNA methylation patterns and understanding how this stable epigenetic mark works to prevent gene activation during development. Aberrant DNA methylation in cancer can be generated either prior to or following cell transformation through mutations. Increasing evidence suggests, however, that most methylation changes are generated in a programmed manner and occur in a subpopulation of tissue cells during normal aging, probably predisposing them for tumorigenesis. It is likely that this methylation contributes to the tumor state by inhibiting the plasticity of cell differentiation processes. Cancer Res; 76(12); 3446–50. ©2016 AACR.
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