GROW-School for Oncology and Developmental Biology, PO Box 616, 6200 Maastricht, The Netherlands.
J Clin Oncol. 2011 Apr 1;29(10):1382-91. doi: 10.1200/JCO.2010.28.2319. Epub 2011 Jan 10.
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.
结直肠癌(CRC)主要被认为是一种遗传疾病,其特征是遗传改变的顺序积累。越来越多的证据表明,表观遗传改变为 CRC 的发病机制增加了一个额外的复杂性层次,并将具有独特病因和预后的结直肠癌亚群进行了特征描述。结直肠癌中的表观遗传失调发生在多个水平,涉及 DNA 甲基化、组蛋白修饰、核小体占据和重塑、染色质环化和非编码 RNA。这些过程之间的相互作用以及与遗传改变的复杂关联最近已经被揭示出来。似乎 CRC 的表观遗传学将成为多步骤致癌发生的范例,就像过去三十年来 CRC 的遗传学一样。这篇综述整合了结直肠癌中基因表达的表观遗传调控的最新数据,并描述了对这些过程的理解将如何改变 CRC 的治疗方法。