表观遗传学
结直肠癌
DNA甲基化
组蛋白
癌变
癌症
后生
医学
染色质
生物
遗传学
疾病
癌症研究
癌症表观遗传学
生物信息学
计算生物学
基因
基因表达
病理
组蛋白甲基转移酶
作者
Manon van Engeland,Sarah Derks,Kim M. Smits,Gerrit A. Meijer,James G. Herman
标识
DOI:10.1200/jco.2010.28.2319
摘要
Colorectal cancer (CRC) has predominantly been considered a genetic disease, characterized by sequential accumulation of genetic alterations. Growing evidence indicates that epigenetic alterations add an additional layer of complexity to the pathogenesis of CRC, and characterize a subgroup of colorectal cancers with a distinct etiology and prognosis. Epigenetic dysregulation in colorectal cancer is organized at multiple levels, involving DNA methylation, histone modifications, nucleosomal occupancy and remodeling, chromatin looping, and noncoding RNAs. Interactions between these processes and complex associations with genetic alterations have recently been unraveled. It appears that CRC epigenetics will be the paradigm for multistep carcinogenesis, as CRC genetics has been for the past three decades. This review integrates recent data on epigenetic regulation of gene expression in CRC and describes how the understanding of these processes will alter the management of CRC.
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