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      Role and mechanism of miRNA in cardiac microvascular endothelial cells in cardiovascular diseases

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          Abstract

          The occurrence and development of myocardial dysfunction are associated with damage in the cardiac microvascular endothelial cells (CMECs), which can regulate nutrient exchange and oxy-gen-carbon cycling to protect cardiomyocytes. Interventions targeting microRNAs (miRNAs) can effectively mitigate CMEC injury and thus improve cardiovascular diseases. MiRNAs are a class of noncoding single-strand RNA molecules typically 21–23 nucleotides in length that are encoded by endogenous genes. They are critical regulators of organism development, cell differentiation, metabolism, and apoptosis. Current clinical trials on miRNA drugs indicate that patient-specific miRNA levels are now being used as one of the criteria for predicting heart disease. However, the cellular process of various miRNAs in CMECs in cardiovascular diseases has not been fully elucidated. These mechanisms are a field that immediately requires further investigation. Accordingly, this review summarizes the roles and mechanisms of various miRNAs in CMECs in cardiovascular disease and includes the process of CMEC crosstalk between miRNAs and other cell types in the heart. Our study serves as a theoretical basis for the formal introduction of miRNA use into the treatment of cardiovascular diseases in the future.

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          Most cited references136

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          MicroRNAs: target recognition and regulatory functions.

          MicroRNAs (miRNAs) are endogenous approximately 23 nt RNAs that play important gene-regulatory roles in animals and plants by pairing to the mRNAs of protein-coding genes to direct their posttranscriptional repression. This review outlines the current understanding of miRNA target recognition in animals and discusses the widespread impact of miRNAs on both the expression and evolution of protein-coding genes.
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            Predicting effective microRNA target sites in mammalian mRNAs

            MicroRNA targets are often recognized through pairing between the miRNA seed region and complementary sites within target mRNAs, but not all of these canonical sites are equally effective, and both computational and in vivo UV-crosslinking approaches suggest that many mRNAs are targeted through non-canonical interactions. Here, we show that recently reported non-canonical sites do not mediate repression despite binding the miRNA, which indicates that the vast majority of functional sites are canonical. Accordingly, we developed an improved quantitative model of canonical targeting, using a compendium of experimental datasets that we pre-processed to minimize confounding biases. This model, which considers site type and another 14 features to predict the most effectively targeted mRNAs, performed significantly better than existing models and was as informative as the best high-throughput in vivo crosslinking approaches. It drives the latest version of TargetScan (v7.0; targetscan.org), thereby providing a valuable resource for placing miRNAs into gene-regulatory networks. DOI: http://dx.doi.org/10.7554/eLife.05005.001
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              Metazoan MicroRNAs

              MicroRNAs (miRNAs) are ∼22 nt RNAs that direct posttranscriptional repression of mRNA targets in diverse eukaryotic lineages. In humans and other mammals, these small RNAs help sculpt the expression of most mRNAs. This article reviews advances in our understanding of the defining features of metazoan miRNAs and their biogenesis, genomics, and evolution. It then reviews how metazoan miRNAs are regulated, how they recognize and cause repression of their targets, and the biological functions of this repression, with a compilation of knockout phenotypes that shows that important biological functions have been identified for most of the broadly conserved miRNAs of mammals.
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                Author and article information

                Contributors
                Journal
                Front Cardiovasc Med
                Front Cardiovasc Med
                Front. Cardiovasc. Med.
                Frontiers in Cardiovascular Medicine
                Frontiers Media S.A.
                2297-055X
                13 March 2024
                2024
                : 11
                : 1356152
                Affiliations
                [ 1 ]Ministry of Education Key Laboratory of Pharmacology of Traditional Chinese Medical Formulae, Tianjin University of Traditional Chinese Medicine , Tianjin, China
                [ 2 ]School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine , Tianjin, China
                [ 3 ]State Key Laboratory of Component-Based Chinese Medicine, Tianjin University of Traditional Chinese Medicine , Tianjin, China
                Author notes

                Edited by: Paul H. A. Quax, Leiden University, Netherlands

                Reviewed by: Teresa Padro, Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau, Spain

                Shafeeq Ahmed Mohammed, University Hospital Zürich, Switzerland

                [* ] Correspondence: Xiaoying Wang wxy@ 123456tjutcm.edu.cn
                Article
                10.3389/fcvm.2024.1356152
                10966125
                38545341
                a2c799c5-60e4-4369-8b10-3770d68c1293
                © 2024 Yan, Zhong, Zhao and Wang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 December 2023
                : 04 March 2024
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 136, Pages: 0, Words: 0
                Funding
                Funded by: National Key R&D Program of China
                Award ID: 2022YFC3500300
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article.
                This research was funded by National Key R&D Program of China (2022YFC3500300).
                Categories
                Cardiovascular Medicine
                Review
                Custom metadata
                Atherosclerosis and Vascular Medicine

                mirna,cardiac microvascular endothelial cell,coronary artery disease,microvascular dysfunction,diabetes,crosstalk

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