Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms17040502
Title: MicroRNA and heart failure
Authors: Wong, L.L 
Wang, J 
Liew, O.W 
Richards, A.M 
Chen, Y.-T 
Keywords: capadenoson
dicer
microRNA
microRNA 1
microRNA 100
microRNA 107
microRNA 122
microRNA 1246
microRNA 1254
microRNA 126
microRNA 133a
microRNA 133b
microRNA 142 3p
microRNA 15
microRNA 17
microRNA 17 5p
microRNA 183 3p
microRNA 18a
microRNA 195
microRNA 208a
microRNA 208b
microRNA 20a
microRNA 499
microRNA 92a
microRNA 92b
mineralocorticoid antagonist
myosin heavy chain alpha
neurohormone
spironolactone
unclassified drug
unindexed drug
hormone
microRNA
apoptosis
biogenesis
clinical trial (topic)
gene expression
gene targeting
heart arrhythmia
heart development
heart failure
heart hypertrophy
heart left ventricle ejection fraction
human
multicenter study (topic)
nonhuman
phase 1 clinical trial (topic)
phase 2 clinical trial (topic)
Review
animal
genetics
heart failure
metabolism
signal transduction
Animals
Heart Failure
Hormones
Humans
MicroRNAs
Signal Transduction
Issue Date: 2016
Citation: Wong, L.L, Wang, J, Liew, O.W, Richards, A.M, Chen, Y.-T (2016). MicroRNA and heart failure. International Journal of Molecular Sciences 17 (4). ScholarBank@NUS Repository. https://doi.org/10.3390/ijms17040502
Rights: Attribution 4.0 International
Abstract: Heart failure (HF) imposes significant economic and public health burdens upon modern society. It is known that disturbances in neurohormonal status play an important role in the pathogenesis of HF. Therapeutics that antagonize selected neurohormonal pathways, specifically the renin-angiotensin-aldosterone and sympathetic nervous systems, have significantly improved patient outcomes in HF. Nevertheless, mortality remains high with about 50% of HF patients dying within five years of diagnosis thus mandating ongoing efforts to improve HF management. The discovery of short noncoding microRNAs (miRNAs) and our increasing understanding of their functions, has presented potential therapeutic applications in complex diseases, including HF. Results from several genome-wide miRNA studies have identified miRNAs differentially expressed in HF cohorts suggesting their possible involvement in the pathogenesis of HF and their potential as both biomarkers and as therapeutic targets. Unravelling the functional relevance of miRNAs within pathogenic pathways is a major challenge in cardiovascular research. In this article, we provide an overview of the role of miRNAs in the cardiovascular system. We highlight several HF-related miRNAs reported from selected cohorts and review their putative roles in neurohormonal signaling. @ 2016 by the authors; licensee MDPI, Basel, Switzerland.
Source Title: International Journal of Molecular Sciences
URI: https://scholarbank.nus.edu.sg/handle/10635/183342
ISSN: 16616596
DOI: 10.3390/ijms17040502
Rights: Attribution 4.0 International
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