An Epigenetic Role of Mitochondria in Cancer

被引:84
作者
Liu, Yu'e [1 ]
Chen, Chao [2 ]
Wang, Xinye [1 ]
Sun, Yihong [1 ]
Zhang, Jin [3 ]
Chen, Juxiang [2 ]
Shi, Yufeng [1 ,4 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Canc Ctr, Sch Med, Shanghai 200092, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Neurosurg, 168 Changhai Rd, Shanghai 200433, Peoples R China
[3] Univ Mississippi, Med Ctr, Dept Pharmacol & Toxicol, Jackson, MS 39216 USA
[4] Tongji Univ, Clin Ctr Brain & Spinal Cord Res, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
mitochondria; epigenetics; cancer; metabolism; ATP-CITRATE LYASE; LINKED N-ACETYLGLUCOSAMINE; DNA METHYLTRANSFERASE 1; ACUTE MYELOID-LEUKEMIA; TUMOR-SUPPRESSOR GENES; EMBRYONIC STEM-CELLS; HISTONE ACETYLATION; O-GLCNAC; ALPHA-KETOGLUTARATE; CPG METHYLATION;
D O I
10.3390/cells11162518
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
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, alpha-ketoglutarate (alpha-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.
引用
收藏
页数:42
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