Department of Medicine, McGill University Health Centre, Montréal, QC, Canada.
Adv Exp Med Biol. 2019;1164:179-196. doi: 10.1007/978-3-030-22254-3_14.
DNA methylation is a chemically reversible epigenetic modification that regulates the chromatin structure and gene expression, and thereby takes part in various cellular processes like embryogenesis, genomic imprinting, X-chromosome inactivation, and genome stability. Alterations in the normal methylation levels of DNA may contribute to the development of pathological conditions like cancer. Even though both hypo- and hypermethylation-mediated abnormalities are prevalent in the cancer genome, the field of cancer epigenetics has been more focused on targeting hypermethylation. As a result, DNA hypomethylation-mediated abnormalities remained relatively less explored, and currently, there are no approved drugs that can be clinically used to target hypomethylation. Understanding the precise role of DNA hypomethylation is not only crucial from a mechanistic point of view but also for the development of pharmacological agents that can reverse the hypomethylated state of the DNA. This chapter focuses on the causes and impact of DNA hypomethylation in the development of cancer and describes the possible ways to pharmacologically target it, especially by using a naturally occurring physiologic agent S-adenosylmethionine (SAM).
DNA 甲基化是一种化学可逆的表观遗传修饰,可调节染色质结构和基因表达,从而参与胚胎发生、基因组印记、X 染色体失活和基因组稳定性等各种细胞过程。DNA 正常甲基化水平的改变可能导致癌症等病理状况的发展。尽管在癌症基因组中普遍存在低甲基化和高甲基化介导的异常,但癌症表观遗传学领域更侧重于针对高甲基化。因此,DNA 低甲基化介导的异常相对较少被探索,目前没有批准的药物可用于临床靶向低甲基化。从机制角度来看,了解 DNA 低甲基化的确切作用不仅至关重要,而且对于开发可逆转 DNA 低甲基化状态的药理学制剂也至关重要。本章重点介绍 DNA 低甲基化在癌症发展中的原因和影响,并描述了通过药理学靶向该过程的可能方法,特别是使用天然存在的生理剂 S-腺苷甲硫氨酸 (SAM)。