Please use this identifier to cite or link to this item:
https://doi.org/10.3390/ijms17050749
DC Field | Value | |
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dc.title | Overview of microRNAs in cardiac hypertrophy, fibrosis, and apoptosis | |
dc.contributor.author | Wang, J | |
dc.contributor.author | Liew, O.W | |
dc.contributor.author | Richards, A.M | |
dc.contributor.author | Chen, Y.-T | |
dc.date.accessioned | 2020-11-10T07:58:04Z | |
dc.date.available | 2020-11-10T07:58:04Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Wang, J, Liew, O.W, Richards, A.M, Chen, Y.-T (2016). Overview of microRNAs in cardiac hypertrophy, fibrosis, and apoptosis. International Journal of Molecular Sciences 17 (5) : 749. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms17050749 | |
dc.identifier.issn | 16616596 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/183337 | |
dc.description.abstract | MicroRNAs (miRNAs) are non-coding RNAs that play essential roles in modulating the gene expression in almost all biological events. In the past decade, the involvement of miRNAs in various cardiovascular disorders has been explored in numerous in vitro and in vivo studies. In this paper, studies focused upon the discovery of miRNAs, their target genes, and functionality are reviewed. The selected miRNAs discussed herein have regulatory effects on target gene expression as demonstrated by miRNA/31 end untranslated region (31UTR) interaction assay and/or gain/loss-of-function approaches. The listed miRNA entities are categorized according to the biological relevance of their target genes in relation to three cardiovascular pathologies, namely cardiac hypertrophy, fibrosis, and apoptosis. Furthermore, comparison across 86 studies identified several candidate miRNAs that might be of particular importance in the ontogenesis of cardiovascular diseases as they modulate the expression of clusters of target genes involved in the progression of multiple adverse cardiovascular events. This review illustrates the involvement of miRNAs in diverse biological signaling pathways and provides an overview of current understanding of, and progress of research into, of the roles of miRNAs in cardiovascular health and disease. @ 2016 by the authors; licensee MDPI, Basel, Switzerland. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | fibronectin | |
dc.subject | guanosine 3' diphosphate 5' triphosphate | |
dc.subject | histone deacetylase 8 | |
dc.subject | microRNA | |
dc.subject | mitogen activated protein kinase | |
dc.subject | somatomedin | |
dc.subject | X box binding protein 1 | |
dc.subject | microRNA | |
dc.subject | apoptosis | |
dc.subject | gene expression | |
dc.subject | gene targeting | |
dc.subject | heart muscle fibrosis | |
dc.subject | heart ventricle hypertrophy | |
dc.subject | loss of function mutation | |
dc.subject | luciferase assay | |
dc.subject | nonhuman | |
dc.subject | oxidative stress | |
dc.subject | protein binding | |
dc.subject | Review | |
dc.subject | signal transduction | |
dc.subject | stress | |
dc.subject | untranslated region | |
dc.subject | animal | |
dc.subject | apoptosis | |
dc.subject | cardiomegaly | |
dc.subject | cardiovascular disease | |
dc.subject | disease model | |
dc.subject | fibrosis | |
dc.subject | gene expression regulation | |
dc.subject | gene regulatory network | |
dc.subject | genetics | |
dc.subject | human | |
dc.subject | metabolism | |
dc.subject | Animals | |
dc.subject | Apoptosis | |
dc.subject | Cardiomegaly | |
dc.subject | Cardiovascular Diseases | |
dc.subject | Disease Models, Animal | |
dc.subject | Fibrosis | |
dc.subject | Gene Expression Regulation | |
dc.subject | Gene Regulatory Networks | |
dc.subject | Humans | |
dc.subject | MicroRNAs | |
dc.subject | Signal Transduction | |
dc.type | Review | |
dc.contributor.department | MEDICINE | |
dc.description.doi | 10.3390/ijms17050749 | |
dc.description.sourcetitle | International Journal of Molecular Sciences | |
dc.description.volume | 17 | |
dc.description.issue | 5 | |
dc.description.page | 749 | |
Appears in Collections: | Staff Publications Elements |
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