Cargando…
miR194 hypomethylation regulates coronary artery disease pathogenesis
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 criti...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759901/ https://www.ncbi.nlm.nih.gov/pubmed/36529725 http://dx.doi.org/10.1186/s12920-022-01421-7 |
_version_ | 1784852335413952512 |
---|---|
author | Duan, Lian Liu, Yongmei Li, Jun Zhang, Yun Liao, Jiangquan Dong, Yan Jie, Wang |
author_facet | Duan, Lian Liu, Yongmei Li, Jun Zhang, Yun Liao, Jiangquan Dong, Yan Jie, Wang |
author_sort | Duan, Lian |
collection | PubMed |
description | 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-022-01421-7. |
format | Online Article Text |
id | pubmed-9759901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97599012022-12-19 miR194 hypomethylation regulates coronary artery disease pathogenesis Duan, Lian Liu, Yongmei Li, Jun Zhang, Yun Liao, Jiangquan Dong, Yan Jie, Wang BMC Med Genomics Research 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-022-01421-7. BioMed Central 2022-12-18 /pmc/articles/PMC9759901/ /pubmed/36529725 http://dx.doi.org/10.1186/s12920-022-01421-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Duan, Lian Liu, Yongmei Li, Jun Zhang, Yun Liao, Jiangquan Dong, Yan Jie, Wang miR194 hypomethylation regulates coronary artery disease pathogenesis |
title | miR194 hypomethylation regulates coronary artery disease pathogenesis |
title_full | miR194 hypomethylation regulates coronary artery disease pathogenesis |
title_fullStr | miR194 hypomethylation regulates coronary artery disease pathogenesis |
title_full_unstemmed | miR194 hypomethylation regulates coronary artery disease pathogenesis |
title_short | miR194 hypomethylation regulates coronary artery disease pathogenesis |
title_sort | mir194 hypomethylation regulates coronary artery disease pathogenesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759901/ https://www.ncbi.nlm.nih.gov/pubmed/36529725 http://dx.doi.org/10.1186/s12920-022-01421-7 |
work_keys_str_mv | AT duanlian mir194hypomethylationregulatescoronaryarterydiseasepathogenesis AT liuyongmei mir194hypomethylationregulatescoronaryarterydiseasepathogenesis AT lijun mir194hypomethylationregulatescoronaryarterydiseasepathogenesis AT zhangyun mir194hypomethylationregulatescoronaryarterydiseasepathogenesis AT liaojiangquan mir194hypomethylationregulatescoronaryarterydiseasepathogenesis AT dongyan mir194hypomethylationregulatescoronaryarterydiseasepathogenesis AT jiewang mir194hypomethylationregulatescoronaryarterydiseasepathogenesis |