表观遗传学
表观遗传学
组蛋白
DNA甲基化
甲基转移酶
机制(生物学)
生物信息学
医学
主动脉夹层
锡尔图因
组蛋白甲基转移酶
生物
基因
遗传学
甲基化
内科学
乙酰化
基因表达
主动脉
认识论
哲学
作者
Tao Yan,Gang Li,Yanyan Yang,Zhibin Wang,Shizhong Wang,Xiaolu Li,Tao Yu,Xiuxiu Fu
出处
期刊:Life Sciences
[Elsevier]
日期:2023-11-06
卷期号:335: 122249-122249
被引量:8
标识
DOI:10.1016/j.lfs.2023.122249
摘要
Aortic dissection (AD) has an unfavorable prognosis. It requires early diagnosis, appropriate treatment strategies, and suspicion to recognize symptoms; thus, it is commonly described as an acute aortic emergency. The clinical manifestations of painless AD are complex and variable. However, there is no effective treatment to prevent the progression of AD. Therefore, study of the molecular targets and mechanisms of AD to enable prevention or early intervention is particularly important. Although multiple gene mutations have been proposed as linked to AD development, evidence that multiple epigenetic elements are strongly associated is steadily increasing. These epigenetic processes include DNA methylation, N6-methyladenosine, histone modification, non-histone posttranslational modification, and non-coding RNAs (ncRNAs). Among these processes, resveratrol targeting Sirtuin 1 (SIRT1), 5-azacytidine (5azaC) targeting DNA methyltransferase (DNMT), and vitamin C targeting ten-eleven translocation 2 (Tet2) showed unique advantages in improving AD and vascular dysfunction. Finally, we explored potential epigenetic drugs and diagnostic methods for AD, which might provide options for the future.
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