Navigating the DNA methylation landscape of cancer

被引:373
|
作者
Nishiyama, Atsuya [1 ]
Nakanishi, Makoto [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Div Canc Cell Biol, Minato Ku, 4-6-1 Shirokanedai, Tokyo 1088639, Japan
关键词
BINDING-PROTEIN MBD2; EMBRYONIC STEM-CELLS; DE-NOVO METHYLATION; HUMAN X-CHROMOSOME; HISTONE H3; TET PROTEINS; MICROSATELLITE INSTABILITY; ABERRANT METHYLATION; EPIGENETIC LANDSCAPE; STRUCTURAL INSIGHT;
D O I
10.1016/j.tig.2021.05.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA methylation is a chemical modification that defines cell type and lineage through the control of gene expression and genome stability. Disruption of DNA methylation control mechanisms causes a variety of diseases, including cancer. Cancer cells are characterized by aberrant DNA methylation (i.e., genome-wide hypomethylation and site-specific hypermethylation), mainly targeting CpG islands in gene expression regulatory elements. In particular, the early findings that a variety of tumor suppressor genes (TSGs) are targets of DNA hypermethylation in cancer led to the proposal of a model in which aberrant DNA methylation promotes cellular oncogenesis through TSGs silencing. However, recent genome-wide analyses have revealed that this classical model needs to be reconsidered. In this review, we will discuss the molecular mechanisms of DNA methylation abnormalities in cancer as well as their therapeutic potential.
引用
收藏
页码:1012 / 1027
页数:16
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