The roles of DNA, RNA and histone methylation in ageing and cancer

染色质 表观遗传学 DNA甲基化 生物 组蛋白 染色质重塑 表观遗传学 组蛋白甲基化 计算生物学 癌症研究 癌症表观遗传学 遗传学 组蛋白甲基转移酶 DNA 基因表达 基因
作者
Ewa M. Michalak,Marian L. Burr,Andrew J. Bannister,Mark A. Dawson
出处
期刊:Nature Reviews Molecular Cell Biology [Springer Nature]
卷期号:20 (10): 573-589 被引量:418
标识
DOI:10.1038/s41580-019-0143-1
摘要

Chromatin is a macromolecular complex predominantly comprising DNA, histone proteins and RNA. The methylation of chromatin components is highly conserved as it helps coordinate the regulation of gene expression, DNA repair and DNA replication. Dynamic changes in chromatin methylation are essential for cell-fate determination and development. Consequently, inherited or acquired mutations in the major factors that regulate the methylation of DNA, RNA and/or histones are commonly observed in developmental disorders, ageing and cancer. This has provided the impetus for the clinical development of epigenetic therapies aimed at resetting the methylation imbalance observed in these disorders. In this Review, we discuss the cellular functions of chromatin methylation and focus on how this fundamental biological process is corrupted in cancer. We discuss methylation-based cancer therapies and provide a perspective on the emerging data from early-phase clinical trial therapies that target regulators of DNA and histone methylation. We also highlight promising therapeutic strategies, including monitoring chromatin methylation for diagnostic purposes and combination epigenetic therapy strategies that may improve immune surveillance in cancer and increase the efficacy of conventional and targeted anticancer drugs. The dynamic methylation of chromatin components — DNA, histones and RNA — is crucial in development, ageing and cancer. Therapies that target regulators of DNA and histone methylation in cancer have recently been developed. These promising therapies, which include strategies that may improve tumour immune surveillance, are already being tested in early-phase clinical trials.
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