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微小 RNA 在心脏纤维化中的功能新见解:从机制到治疗策略。

New Insights into the Functions of MicroRNAs in Cardiac Fibrosis: From Mechanisms to Therapeutic Strategies.

机构信息

Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

Key Laboratory of Organ Transplantation, Ministry of Education, and NHC Key Laboratory of Organ Transplantation, Wuhan 430030, China.

出版信息

Genes (Basel). 2022 Aug 4;13(8):1390. doi: 10.3390/genes13081390.

DOI:10.3390/genes13081390
PMID:36011301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9407613/
Abstract

Cardiac fibrosis is a significant global health problem associated with almost all types of heart disease. Extensive cardiac fibrosis reduces tissue compliance and contributes to adverse outcomes, such as cardiomyocyte hypertrophy, cardiomyocyte apoptosis, and even heart failure. It is mainly associated with pathological myocardial remodeling, characterized by the excessive deposition of extracellular matrix (ECM) proteins in cardiac parenchymal tissues. In recent years, a growing body of evidence demonstrated that microRNAs (miRNAs) have a crucial role in the pathological development of cardiac fibrosis. More than sixty miRNAs have been associated with the progression of cardiac fibrosis. In this review, we summarized potential miRNAs and miRNAs-related regulatory mechanisms for cardiac fibrosis and discussed the potential clinical application of miRNAs in cardiac fibrosis.

摘要

心肌纤维化是一个全球性的重大健康问题,几乎与所有类型的心脏病都有关。广泛的心肌纤维化降低了组织顺应性,并导致不良后果,如心肌细胞肥大、心肌细胞凋亡,甚至心力衰竭。它主要与病理性心肌重构有关,其特征是心肌实质组织中细胞外基质(ECM)蛋白的过度沉积。近年来,越来越多的证据表明 microRNAs(miRNAs)在心肌纤维化的病理发展中起着关键作用。有六十多种 miRNAs 与心肌纤维化的进展有关。在这篇综述中,我们总结了潜在的 miRNAs 及其与心肌纤维化相关的调节机制,并讨论了 miRNAs 在心肌纤维化中的潜在临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/908f2d2fd0bb/genes-13-01390-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/b16f9df15ea3/genes-13-01390-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/696b59a78e7b/genes-13-01390-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/bcd029d1d3f6/genes-13-01390-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/908f2d2fd0bb/genes-13-01390-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/b16f9df15ea3/genes-13-01390-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/696b59a78e7b/genes-13-01390-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/bcd029d1d3f6/genes-13-01390-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf30/9407613/908f2d2fd0bb/genes-13-01390-g004.jpg

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2
Photobiomodulation therapy's effects on cardiac fibrosis activation after experimental myocardial infarction.光生物调节疗法对实验性心肌梗死后心肌纤维化激活的影响。
Lasers Surg Med. 2022 Aug;54(6):883-894. doi: 10.1002/lsm.23544. Epub 2022 Apr 2.
3
Non-canonical features of microRNAs: paradigms emerging from cardiovascular disease.
心肌细胞作为细胞外囊泡货物分泌的miR-24-3p可抑制人心脏微组织中的纤维化。
Cardiovasc Res. 2025 Apr 15;121(1):143-156. doi: 10.1093/cvr/cvae243.
4
Regulation of idiopathic pulmonary fibrosis: a cross-talk between TGF- signaling and MicroRNAs.特发性肺纤维化的调控:转化生长因子信号与微小RNA之间的相互作用
Front Med (Lausanne). 2024 Sep 25;11:1415278. doi: 10.3389/fmed.2024.1415278. eCollection 2024.
5
Endoplasmic reticulum stress signaling modulates ischemia/reperfusion injury in the aged heart by regulating mitochondrial maintenance.内质网应激信号通过调节线粒体维持来调节老年心脏的缺血/再灌注损伤。
Mol Med. 2024 Jul 23;30(1):107. doi: 10.1186/s10020-024-00869-w.
6
Unraveling the Cardiac Matrix: From Diabetes to Heart Failure, Exploring Pathways and Potential Medications.解析心脏基质:从糖尿病到心力衰竭,探寻相关途径及潜在药物
Biomedicines. 2024 Jun 13;12(6):1314. doi: 10.3390/biomedicines12061314.
7
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iScience. 2024 May 23;27(6):110084. doi: 10.1016/j.isci.2024.110084. eCollection 2024 Jun 21.
8
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9
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10
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J Transl Med. 2024 Feb 1;22(1):124. doi: 10.1186/s12967-024-04900-w.
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Nat Rev Cardiol. 2022 Sep;19(9):620-638. doi: 10.1038/s41569-022-00680-2. Epub 2022 Mar 18.
4
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5
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J Cardiovasc Transl Res. 2021 Dec;14(6):1051-1062. doi: 10.1007/s12265-021-10116-w. Epub 2021 Mar 15.
9
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Int J Cardiol. 2021 Jun 1;332:35-37. doi: 10.1016/j.ijcard.2021.02.088. Epub 2021 Mar 5.
10
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Front Pharmacol. 2021 Jan 14;11:572637. doi: 10.3389/fphar.2020.572637. eCollection 2020.