摘要
微RNA(miRNAs)是小的非编码RNAs,作为基因表达的转录后调控因子。过去20年的研究已经揭示了这些小分子可作为治疗性靶点或者CVD的制剂的潜力。此外, 在这个循环中或其他体液的miRNAs是稳定的并且容易被检测,更重要的是与疾病相关,使他们成为CVDs诊断和预后的生物标记物。此外,有证明揭示了miRNA作为心血管新的靶点药物的调节器,miRNAs能够与一些药物发生反应并且为新型CVD药物的研究与发展发展了新的机遇。在此,本文综述了当前关于miRNAs在CVD治疗中潜在的应用的知识,包括心肌缺血、心脏肥大、心衰、间质性纤维化、心率失常、糖尿病和高血压,并且讨论了miRNAs在药物研发中治疗性的潜力和挑战。
关键词: 微RNA(miRNA),药物发现,心肌缺血,心脏肥大,心肌纤维化,心率失常,心衰,高血压,糖尿病,生物标记物
图形摘要
Current Drug Targets
Title:MicroRNAs as Candidate Drug Targets for Cardiovascular Diseases
Volume: 18 Issue: 4
关键词: 微RNA(miRNA),药物发现,心肌缺血,心脏肥大,心肌纤维化,心率失常,心衰,高血压,糖尿病,生物标记物
摘要: MicroRNAs (miRNAs) are small conserved noncoding RNAs which function as posttranscriptional regulators of gene expression. Studies over the last 20 years have revealed the essential functions of miRNAs in regulating cardiovascular biology (such as cardiovascular cell differentiation, growth, proliferation and apoptosis) and crucial roles in controlling cardiovascular disease (CVD), indicating the potential of these small molecules as therapeutic targets and/or agents for CVD. Moreover, miRNAs in the circulation or other body fluids are stable and readily detectable, and more importantly often disease-associated, which makes them promising novel biomarkers for diagnosis and prognosis of CVDs. Furthermore, emerging evidence uncovered miRNAs as new targets and/or regulators of cardiovascular medications given the ability of miRNAs to interact with some cardiovascular drugs, which opens up new opportunities for the research and development of novel CVD drugs. Herein, we summarize current knowledge regarding the potential applications of miRNAs in the therapy of CVD, including myocardial ischemia, cardiac hypertrophy/heart failure, interstitial fibrosis, arrhythmia, diabetes and hypertension and discuss the therapeutic potential and challenge of miRNAs in drug discovery.
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Cite this article as:
MicroRNAs as Candidate Drug Targets for Cardiovascular Diseases, Current Drug Targets 2017; 18 (4) . https://dx.doi.org/10.2174/1389450117666160301101221
DOI https://dx.doi.org/10.2174/1389450117666160301101221 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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