Epigenetics of colorectal cancer: biomarker and therapeutic potential

表观遗传学 医学 DNA甲基化 结直肠癌 疾病 生物信息学 癌症 生物标志物 恶性肿瘤 内科学 组蛋白 生物标志物发现 生物 遗传学 病理 蛋白质组学 基因 基因表达
作者
Gerhard Jung,Eva Hernández‐Illán,Leticia Moreira,Francesc Balaguer,Ajay Goel
出处
期刊:Nature Reviews Gastroenterology & Hepatology [Springer Nature]
卷期号:17 (2): 111-130 被引量:528
标识
DOI:10.1038/s41575-019-0230-y
摘要

Colorectal cancer (CRC), a leading cause of cancer-related death worldwide, evolves as a result of the stepwise accumulation of a series of genetic and epigenetic alterations in the normal colonic epithelium, leading to the development of colorectal adenomas and invasive adenocarcinomas. Although genetic alterations have a major role in a subset of CRCs, the pathophysiological contribution of epigenetic aberrations in this malignancy has attracted considerable attention. Data from the past couple of decades has unequivocally illustrated that epigenetic marks are important molecular hallmarks of cancer, as they occur very early in disease pathogenesis, involve virtually all key cancer-associated pathways and, most importantly, can be exploited as clinically relevant disease biomarkers for diagnosis, prognostication and prediction of treatment response. In this Review, we summarize the current knowledge on the best-studied epigenetic modifications in CRC, including DNA methylation and histone modifications, as well as the role of non-coding RNAs as epigenetic regulators. We focus on the emerging potential for the bench-to-bedside translation of some of these epigenetic alterations into clinical practice and discuss the burgeoning evidence supporting the potential of emerging epigenetic therapies in CRC as we usher in the era of precision medicine. Epigenetic modifications and regulators, including DNA methylation, histone modifications and non-coding RNA species, have key pathophysiological roles in colorectal cancer (CRC). This Review outlines these epigenetic aberrations in CRC and their potential as diagnostic, prognostic and predictive biomarkers and therapeutic targets.
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