DNA methylation, smooth muscle cells, and atherogenesis

被引:86
作者
Hiltunen, MO
Ylä-Herttuala, S
机构
[1] Univ Kuopio, Dept Mol Med, AI Virtanen Inst, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Med, FIN-70211 Kuopio, Finland
[3] Kuopio Univ Hosp, Gene Therapy Unit, SF-70210 Kuopio, Finland
关键词
atherogenesis; DNA methylation; 5-methylcytosine; epigenetic gene regulation; gene expression;
D O I
10.1161/01.ATV.0000092871.30563.41
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
DNA methylation is a form of epigenetic modification of the genome that can regulate gene expression. Hypermethylation of CpG islands in the promoter areas leads to decreased gene expression, whereas promoters of actively transcribed genes remain nonmethylated. Because of cellular proliferation and monoclonality of at least some of the lesion cells, atherosclerotic lesions have been compared with benign vascular tumors.(1,2) However, although genetic and epigenetic background favors neoplastic transformation, atherosclerotic plaques never develop to malignant tumors. Among cancer cells, common features are genome-wide hypomethylation, which correlates with transformation and tumor progression. Recent studies have shown that DNA methylation changes occur also during atherogenesis and may contribute to the lesion development.
引用
收藏
页码:1750 / 1753
页数:4
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