| Literature DB >> 29653065 |
Yami Liu1, Wen Peng2, Kai Qu3, Xiaolong Lin4, Zhaolin Zeng1, Jiaojiao Chen1, Dangheng Wei1, Zuo Wang1.
Abstract
Atherosclerosis is the underlying cause of cardio-cerebrovascular disease. However, the mechanisms of atherosclerosis are still unclear. The modification of DNA methylation has an important role in atherosclerosis development. As a member of the Ten-eleven translocation (TET) family, TET methylcytosine dioxygenase 2 (TET2) can modify DNA methylation by catalyzing 5-methylcytosine to 5-hydroxymethylcytosine and mediate DNA demethylation. Recent findings suggest that TET2 is related to the phenotype transformation of vascular smooth muscle cells, endothelial dysfunction, and inflammation of macrophage, the key factors of atherosclerosis. Therefore, TET2 may be a potential target for atherosclerosis treatment. This review will elaborate the recent findings that suggest the role of TET2 in atherosclerosis.Entities:
Keywords: DNA demethylation; TET2; atherosclerosis; inflammation
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Year: 2018 PMID: 29653065 PMCID: PMC5985959 DOI: 10.1089/dna.2017.4118
Source DB: PubMed Journal: DNA Cell Biol ISSN: 1044-5498 Impact factor: 3.311