摘要
背景:由于它们在循环中的特殊稳定性,microRNA(miR)被鉴定为有希望的生物标志物。另一方面,他们调节功能密切相关基因网络的倾向和相对的交付方便性使其成为治疗的有吸引力的目标。 然而,两种应用都没有挑战,特别是适用于缺血性冠状动脉疾病(CAD)。 目的:本研究将:1)描述最常见的与最常见的CAD表现相关的miR,包括动脉粥样硬化,心绞痛,心肌梗塞和通过动脉发生的心肌再灌注,2)强调那些也被改变的miR在代谢综合征及其组成病理学中,3)讨论目前预防与细胞培养,动物模型和人类研究结果不一致的临床应用的挑战以及技术挑战,以及4)对这些差异的解决方案提出一些建议。 结论:虽然miR可用作心肌梗死的可靠生物标志物,但其作为其他形式缺血性CAD的生物标志物,以及CAD治疗等待进一步研究。
关键词: 生物标志物,冠状动脉疾病,代谢综合征,微小RNA,心肌缺血。
图形摘要
Current Drug Targets
Title:Can microRNAs be Biomarkers or Targets for Therapy of Ischemic Coronary Artery Disease in Metabolic Syndrome?
Volume: 18 Issue: 15
关键词: 生物标志物,冠状动脉疾病,代谢综合征,微小RNA,心肌缺血。
摘要: Background: Due to their exceptional stability in the circulation, microRNAs (miRs) are being identified as promising biomarkers. On the other hand, their propensity to regulate networks of functionally closely related genes and relative ease of delivery makes them attractive targets for therapy. However, neither application is without challenges, especially as it applies to ischemic coronary artery disease (CAD).
Objective: This review will: 1) describe miRs which have been most consistently found to be associated with the most common manifestations of CAD, including atherosclerosis, angina pectoris, myocardial infarction and myocardial reperfusion through arteriogenesis, 2) emphasize those miRs which are also altered in metabolic syndrome and its component pathologies, 3) discuss challenges which currently prevent clinical application related to inconsistencies between findings in cell culture, animal models and among human studies, as well as technical challenges, and 4) offer some suggestions towards resolutions of these discrepancies.
Conclusion: While miRs can be used as reliable biomarkers for myocardial infarction, their use as biomarkers for other forms of ischemic CAD, as well as therapy for CAD await further investigation.
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Cite this article as:
Can microRNAs be Biomarkers or Targets for Therapy of Ischemic Coronary Artery Disease in Metabolic Syndrome?, Current Drug Targets 2017; 18 (15) . https://dx.doi.org/10.2174/1389450117666160201113734
DOI https://dx.doi.org/10.2174/1389450117666160201113734 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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