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MicroRNA in cardiovascular biology and disease.

TLDR
In this paper, a review discusses emerging functions of miRNAs in cardiogenesis, heart regeneration and the pathophysiology of cardiovascular diseases, including myocardial infarction, hypertrophy, fibrosis, heart failure, arrhythmia, inflammation and atherosclerosis.
Abstract
MicroRNAs (miRNAs) are members of a non-coding RNA family. They act as negative regulators of protein translation by affecting messenger RNA (mRNA) stability; they modulate numerous signaling pathways and cellular processes, and are involved in cell-to-cell communication. Thus, studies on miRNAs offer an opportunity to improve our understanding of complex biological mechanisms. In the cardiovascular system, miRNAs control functions of various cells, such as cardiomyocytes, endothelial cells, smooth muscle cells and fibroblasts. The pivotal role of miRNAs in the cardiovascular system provides a new perspective on the pathophysiology of disorders like myocardial infarction, hypertrophy, fibrosis, heart failure, arrhythmia, inflammation and atherosclerosis. MiRNAs are differentially expressed in diseased tissue and can be released into circulation. Manipulation of miRNA activity may influence the course of a disease. Therefore, miRNAs have become an active field of research for developing new diagnostic and therapeutic tools. This review discusses emerging functions of miRNAs in cardiogenesis, heart regeneration and the pathophysiology of cardiovascular diseases.

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Targeting mitochondria for cardiovascular disorders: therapeutic potential and obstacles

TL;DR: The therapeutic potential of targeting mitochondria in patients with cardiovascular disease is discussed, the obstacles that have restrained the development of mitochondria-targeting agents thus far are examined, and strategies that might empower the full clinical potential of this approach are identified.
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MicroRNAs in Cardiac Diseases.

TL;DR: This review summarizes and updates microRNAs playing a role in the different processes underlying the pathogenic phenotypes of cardiac muscle and highlights their potential role as disease biomarkers and therapeutic targets.
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Inhibition of circHIPK3 prevents angiotensin II-induced cardiac fibrosis by sponging miR-29b-3p

TL;DR: The data suggest that circHIPK3 serves as a miR-29b-3p sponge to regulate CF proliferation, migration and development of cardiac fibrosis, revealing a potential new target for the prevention of Ang II-induced cardiac fibrot.
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Recent Advances in miRNA Delivery Systems

TL;DR: In this paper, the strengths and weaknesses of current state-of-the-art viral and non-viral miRNA delivery systems and how these tools can be exploited to improve the outcomes of miRNA-based therapeutics.
Journal ArticleDOI

Oxidative Stress-Responsive MicroRNAs in Heart Injury.

TL;DR: The need for studying the role of redox-sensitive miRNAs is pointed to to identify more effective biomarkers and develop better therapeutic targets for oxidative-stress-related heart diseases.
References
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Journal ArticleDOI

Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement

TL;DR: A structured summary is provided including, as applicable, background, objectives, data sources, study eligibility criteria, participants, interventions, study appraisal and synthesis methods, results, limitations, conclusions and implications of key findings.
Journal ArticleDOI

Zirconia as a ceramic biomaterial

TL;DR: This review takes into account the main results achieved up to now, and is focused on the role that microstructural characteristics play on the TZP ceramics behaviour in ball heads, namely mechanical properties and their stability, wear of the UHMWPE paired to TZp, and their influence on biocompatibility.
Journal ArticleDOI

Dysregulation of microRNAs after myocardial infarction reveals a role of miR-29 in cardiac fibrosis

TL;DR: It is concluded that miR-29 acts as a regulator of cardiac fibrosis and represents a potential therapeutic target for tissue fibrosis in general.
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