表观基因组
表观遗传学
染色质
生物
组蛋白
乙酰化
癌变
细胞生物学
细胞代谢
新陈代谢
癌细胞
DNA甲基化
癌症
生物化学
遗传学
DNA
基因表达
基因
作者
Alessandro Carrer,Kathryn E. Wellen
标识
DOI:10.1016/j.copbio.2014.11.012
摘要
Both cellular nutrient metabolism and chromatin organization are remodeled in cancer cells, and these alterations play key roles in tumor development and growth. Many chromatin modifying-enzymes utilize metabolic intermediates as cofactors or substrates, and recent studies have demonstrated that the epigenome is sensitive to cellular metabolism. The contribution of metabolic alterations to epigenetic deregulation in cancer cells is just beginning to emerge, as are the roles of the metabolism-epigenetics link in tumorigenesis. Here we review the roles of acetyl-CoA and S-adenosylmethionine (SAM), donor substrates for acetylation and methylation reactions, respectively, in regulating chromatin modifications in response to nutrient metabolism. We further discuss how oncogenic signaling, cell metabolism, and histone modifications are interconnected and how their relationship might impact tumor growth.
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