Epigenetic
gene deregulation in cancer commonly occurs through chromatin repression and
promoter hypermethylation of tumor-associated genes. However, the mechanism
underpinning epigenetic-based gene activation in carcinogenesis is still poorly
understood. Here, we identify a mechanism of domain gene deregulation through
coordinated long-range epigenetic activation (LREA) of regions that typically
span 1 Mb and harbor key oncogenes, microRNAs, and cancer biomarker genes. Gene
promoters within LREA domains are characterized by a gain of active chromatin
marks and a loss of repressive marks. Notably, although promoter
hypomethylation is uncommon, we show that extensive DNA hypermethylation of CpG
islands or "CpG-island borders" is strongly related to
cancer-specific gene activation or differential promoter usage. These findings
have wide ramifications for cancer diagnosis, progression, and epigenetic-based
gene therapies.
Source: Regional
activation of the cancer genome by long-range epigenetic remodeling. Bert SA,
Robinson MD, Strbenac D, Statham AL, Song JZ, Hulf T, Sutherland RL, Coolen MW,
Stirzaker C, Clark SJ. Cancer Cell. 2013 Jan 14;23(1):9-22.
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