Author: Park, Jae-Ho; Kho, Changwon
Title: MicroRNAs and Calcium Signaling in Heart Disease Cord-id: qn2kz0n9 Document date: 2021_9_30
ID: qn2kz0n9
Snippet: In hearts, calcium (Ca(2+)) signaling is a crucial regulatory mechanism of muscle contraction and electrical signals that determine heart rhythm and control cell growth. Ca(2+) signals must be tightly controlled for a healthy heart, and the impairment of Ca(2+) handling proteins is a key hallmark of heart disease. The discovery of microRNA (miRNAs) as a new class of gene regulators has greatly expanded our understanding of the controlling module of cardiac Ca(2+) cycling. Furthermore, many studi
Document: In hearts, calcium (Ca(2+)) signaling is a crucial regulatory mechanism of muscle contraction and electrical signals that determine heart rhythm and control cell growth. Ca(2+) signals must be tightly controlled for a healthy heart, and the impairment of Ca(2+) handling proteins is a key hallmark of heart disease. The discovery of microRNA (miRNAs) as a new class of gene regulators has greatly expanded our understanding of the controlling module of cardiac Ca(2+) cycling. Furthermore, many studies have explored the involvement of miRNAs in heart diseases. In this review, we aim to summarize cardiac Ca(2+) signaling and Ca(2+)-related miRNAs in pathological conditions, including cardiac hypertrophy, heart failure, myocardial infarction, and atrial fibrillation. We also discuss the therapeutic potential of Ca(2+)-related miRNAs as a new target for the treatment of heart diseases.
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