Tse Janson W T, Jenkins Laura J, Chionh Fiona, Mariadason John M
Olivia Newton-John Cancer Research Institute, Melbourne, Australia; These authors contributed equally.
Olivia Newton-John Cancer Research Institute, Melbourne, Australia; School of Cancer Medicine, La Trobe University, Melbourne, Australia; These authors contributed equally.
Trends Cancer. 2017 Oct;3(10):698-712. doi: 10.1016/j.trecan.2017.08.003. Epub 2017 Sep 12.
Colorectal cancers (CRCs) are characterized by global hypomethylation and promoter-specific DNA methylation. A subset of CRCs with extensive and co-ordinate patterns of promoter methylation has also been identified, termed the CpG-island methylator phenotype. Some genes methylated in CRC are established tumor suppressors; however, for the majority, direct roles in disease initiation or progression have not been established. Herein, we examine functional evidence of specific methylated genes contributing to CRC pathogenesis, focusing on components of commonly deregulated signaling pathways. We also review current knowledge of the mechanisms underpinning promoter methylation in CRC, including genetic events, altered transcription factor binding, and DNA damage. Finally, we summarize clinical trials of DNA methyltransferase inhibitors in CRC, and propose strategies for enhancing their efficacy.
结直肠癌(CRCs)的特征是全基因组低甲基化和启动子特异性DNA甲基化。还鉴定出了一部分具有广泛且协调的启动子甲基化模式的结直肠癌,称为CpG岛甲基化表型。在结直肠癌中甲基化的一些基因是已确定的肿瘤抑制基因;然而,对于大多数基因而言,其在疾病起始或进展中的直接作用尚未明确。在此,我们研究特定甲基化基因对结直肠癌发病机制作用的功能证据,重点关注常见失调信号通路的组成部分。我们还回顾了目前关于结直肠癌中启动子甲基化基础机制的知识,包括遗传事件、转录因子结合改变和DNA损伤。最后,我们总结了结直肠癌中DNA甲基转移酶抑制剂的临床试验,并提出提高其疗效的策略。