4.5 Article

miR194 hypomethylation regulates coronary artery disease pathogenesis

期刊

BMC MEDICAL GENOMICS
卷 15, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12920-022-01421-7

关键词

Coronary artery disease; DNA methylation; miRNA; MAPK; Apoptosis

资金

  1. National Natural Science Foundation of China
  2. Excellent young scientific and technological talents of China Academy of Chinese Medicine Sciences [81473561, 81904185]
  3. [ZZ14-YQ-015]

向作者/读者索取更多资源

This study reveals a unique regulatory network for coronary artery disease (CAD) through DNA methylation assays, miRNA and mRNA sequencing, and bioinformatics analyses. It also identifies a potential therapeutic target for CAD.
Coronary artery disease (CAD) is one of the most common heart diseases, characterized by the hardening and narrowing of arteries, resisting blood supply to cardiac muscle. Despite extensive research, the pathogenesis and therapeutic options for CAD remain limited. Epigenetic regulation plays a critical role in CAD progression. Here, we report a unique DNA methylation-miRNA-mRNA regulatory network for CAD, delineated through DNA methylation assays, miRNA and mRNA sequencing, bioinformatics analyses. We also identified key signaling pathways in this network, including the miR194 promoter-miR194-MAPK signaling pathway by pyrosequencing, methylation PCR, qRT-PCR. This pathway could play a role in CAD by apoptosis. Our findings suggested that this signaling pathway may be a potential therapeutic target for CAD. We believe that our study significantly contributes to an improved understanding of the role of specific miRNAs methylation, miRNA, and mRNAs in CAD pathogenesis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据