The epigenetics of (hereditary) colorectal cancer

被引:57
作者
Venkatachalam, Ramprasath [1 ]
Ligtenberg, Marjolijn J. L. [1 ]
Hoogerbrugge, Nicoline [1 ]
de Bruijn, Diederik R. H. [1 ]
Kuiper, Roland P. [1 ]
van Kessel, Ad Geurts [1 ]
机构
[1] Radboud Univ Nijmegen, Ctr Oncol, Dept Human Genet, Med Ctr,Nijmegen Ctr for Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
关键词
ISLAND METHYLATOR PHENOTYPE; CHROMATIN REMODELING COMPLEXES; MICROSATELLITE INSTABILITY; COLON-CANCER; DNA METHYLATION; BRAF MUTATION; JUVENILE POLYPOSIS; GERMLINE EPIMUTATION; HISTONE DEACETYLASE; ANTISENSE RNA;
D O I
10.1016/j.cancergencyto.2010.08.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
In the last decade, it has become apparent that not only DNA sequence variations but also epigenetic modifications may contribute to disease, including cancer. These epigenetic modifications involve histone modification including acetylation and methylation. DNA methylation, and chromatin remodeling. One of the best-characterized epigenetic changes is aberrant inethylation of cytosines that occur in so-called CpG islands. DNA hypomethylation, prevalent as a genome-wide event, usually occurs in more advanced stages of tumor development. In contrast, DNA hypermethylation is often observed as a discrete, targeted event within tumor cells, resulting in specific loss of gene expression. Interestingly, it was found that sporadic and inherited cancers may exhibit similar DNA methylation patterns, and many genes that are mutated in familial cancers have also been found to be hypermethylated, mutated, or deleted in sporadic cancers. In this review, we will focus on DNA methylation events as heritable epimutations predisposing to colorectal cancer development. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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