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非编码RNA时代的主动脉瓣钙化:主动脉瓣狭窄管理即将迎来的变革?

Aortic valve calcification in the era of non-coding RNAs: The revolution to come in aortic stenosis management?

作者信息

Nader Joseph, Metzinger Laurent, Maitrias Pierre, Caus Thierry, Metzinger-Le Meuth Valérie

机构信息

Department of Cardiac Surgery, Amiens University Hospital, Amiens, France.

HEMATIM EA4666, C.U.R.S, Université de Picardie Jules Verne, 80025, AMIENS Cedex 1, France.

出版信息

Noncoding RNA Res. 2020 Feb 29;5(2):41-47. doi: 10.1016/j.ncrna.2020.02.005. eCollection 2020 Jun.

DOI:10.1016/j.ncrna.2020.02.005
PMID:32195449
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7075756/
Abstract

Aortic valve stenosis remains the most frequent structural heart disease, especially in the elderly. During the last decade, we noticed an important consideration and a huge number of publications related to the medical and surgical treatment of this disease. However, the molecular aspect of this degenerative issue has also been more widely studied recently. As evidenced in oncologic but also cardiac research fields, the emergence of microRNAs in the molecular screening and follow-up makes them potential biomarkers in the future, for the diagnosis, follow-up and treatment of aortic stenosis. Herein, we present a review on the implication of microRNAs in the aortic valve disease management. After listing and describing the main miRNAs of interest in the field, we provide an outline to develop miRNAs as innovative biomarkers and innovative therapeutic strategies, and describe a groundbreaking pre-clinical study using inhibitors of miR-34a in a pre-clinical model of aortic valve stenosis.

摘要

主动脉瓣狭窄仍然是最常见的结构性心脏病,尤其是在老年人中。在过去十年中,我们注意到对这种疾病的医学和外科治疗有了重要的关注以及大量的相关出版物。然而,最近对这个退行性问题的分子层面也进行了更广泛的研究。正如在肿瘤学以及心脏研究领域所证明的那样,微小RNA在分子筛查和随访中的出现使其在未来有可能成为主动脉瓣狭窄诊断、随访和治疗的潜在生物标志物。在此,我们对微小RNA在主动脉瓣疾病管理中的作用进行综述。在列出并描述该领域主要感兴趣的微小RNA后,我们概述了将微小RNA开发为创新生物标志物和创新治疗策略的方法,并描述了一项在主动脉瓣狭窄临床前模型中使用miR-34a抑制剂的开创性临床前研究。

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引用本文的文献

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What can we do to improve the diagnosis and treatment of aortic stenosis?我们可以做些什么来改善主动脉瓣狭窄的诊断和治疗?
Br J Cardiol. 2023 Jan 18;30(1):1. doi: 10.5837/bjc.2023.001. eCollection 2023.
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miRNA in Ischemic Heart Disease and Its Potential as Biomarkers: A Comprehensive Review.miRNA 在缺血性心脏病中的作用及其作为生物标志物的潜力:全面综述。
Int J Mol Sci. 2022 Aug 12;23(16):9001. doi: 10.3390/ijms23169001.
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The mechanistic pathways of oxidative stress in aortic stenosis and clinical implications.氧化应激在主动脉瓣狭窄中的作用机制及其临床意义。

本文引用的文献

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J Cancer. 2019 Jul 23;10(18):4430-4441. doi: 10.7150/jca.30313. eCollection 2019.
2
Therapeutic inhibition of microRNA-34a ameliorates aortic valve calcification via modulation of Notch1-Runx2 signalling.治疗性抑制 microRNA-34a 通过调节 Notch1-Runx2 信号改善主动脉瓣钙化。
Cardiovasc Res. 2020 Apr 1;116(5):983-994. doi: 10.1093/cvr/cvz210.
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Stool-Based miR-92a and miR-144* as Noninvasive Biomarkers for Colorectal Cancer Screening.
Theranostics. 2022 Jul 4;12(11):5189-5203. doi: 10.7150/thno.71813. eCollection 2022.
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Aortic valve disease in diabetes: Molecular mechanisms and novel therapies.糖尿病性主动脉瓣疾病:分子机制与新型治疗策略。
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Telocytes-derived extracellular vesicles alleviate aortic valve calcification by carrying miR-30b.间质细胞衍生的细胞外囊泡通过携带 miR-30b 减轻主动脉瓣钙化。
ESC Heart Fail. 2021 Oct;8(5):3935-3946. doi: 10.1002/ehf2.13460. Epub 2021 Jun 24.
基于粪便的 miR-92a 和 miR-144* 作为结直肠癌筛查的非侵入性生物标志物。
Oncology. 2019;97(3):173-179. doi: 10.1159/000500639. Epub 2019 Jun 19.
4
MiRNA profiling revealed enhanced susceptibility to oxidative stress of endothelial cells from bicuspid aortic valve.miRNA 谱分析显示二叶式主动脉瓣内皮细胞对氧化应激的易感性增强。
J Mol Cell Cardiol. 2019 Jun;131:146-154. doi: 10.1016/j.yjmcc.2019.04.024. Epub 2019 Apr 23.
5
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Noncoding RNA Res. 2019 Jan 23;4(1):30-35. doi: 10.1016/j.ncrna.2019.01.002. eCollection 2019 Mar.
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N Engl J Med. 2019 May 2;380(18):1695-1705. doi: 10.1056/NEJMoa1814052. Epub 2019 Mar 16.
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N Engl J Med. 2019 May 2;380(18):1706-1715. doi: 10.1056/NEJMoa1816885. Epub 2019 Mar 16.
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