表观遗传学
生物
癌变
线粒体
组蛋白
DNA甲基化
细胞命运测定
神经发生的表观遗传调控
细胞代谢
细胞生物学
癌症
细胞
遗传学
基因
基因表达
组蛋白甲基转移酶
转录因子
作者
Yue Liu,Chao Chen,Xinye Wang,Yihong Sun,Jin Zhang,Juxiang Chen,Yufeng Shi
出处
期刊:Cells
[MDPI AG]
日期:2022-08-13
卷期号:11 (16): 2518-2518
被引量:67
标识
DOI:10.3390/cells11162518
摘要
Mitochondria are not only the main energy supplier but are also the cell metabolic center regulating multiple key metaborates that play pivotal roles in epigenetics regulation. These metabolites include acetyl-CoA, α-ketoglutarate (α-KG), S-adenosyl methionine (SAM), NAD+, and O-linked beta-N-acetylglucosamine (O-GlcNAc), which are the main substrates for DNA methylation and histone post-translation modifications, essential for gene transcriptional regulation and cell fate determination. Tumorigenesis is attributed to many factors, including gene mutations and tumor microenvironment. Mitochondria and epigenetics play essential roles in tumor initiation, evolution, metastasis, and recurrence. Targeting mitochondrial metabolism and epigenetics are promising therapeutic strategies for tumor treatment. In this review, we summarize the roles of mitochondria in key metabolites required for epigenetics modification and in cell fate regulation and discuss the current strategy in cancer therapies via targeting epigenetic modifiers and related enzymes in metabolic regulation. This review is an important contribution to the understanding of the current metabolic-epigenetic-tumorigenesis concept.
科研通智能强力驱动
Strongly Powered by AbleSci AI