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RNA 结合蛋白与心血管疾病中的非编码 RNA

RNA Binding Proteins and Non-coding RNA's in Cardiovascular Diseases.

机构信息

University Centre of Excellence in Research, Baba Farid University of Health Sciences, Faridkot, Punjab, India.

Multidisciplinary Research Unit, Guru Gobind Singh Medical College, Faridkot, Punjab, India.

出版信息

Adv Exp Med Biol. 2020;1229:105-118. doi: 10.1007/978-981-15-1671-9_5.

Abstract

Cardiovascular disease (CVD) is the leading cause of mortality as well as morbidity worldwide. The disease has been reported to be chronic in nature and the symptoms of the disease worsen progressively over a long period of time. Inspite of noteworthy achievements have been made in the therapy of CVD yet the available drugs are associated with various undesirable factors including drug toxicity, complexity, resistance and many more. The versatility of RNAs makes them crucial therapeutics candidate for many human diseases. Deeper understanding of RNA biology, exploring new classes of RNA that possess therapeutic potential will help in its successful translation to the clinic. Understanding the mode of action of various RNAs such as miRNA, RNA binding proteins and siRNA in CVD will help in improved therapeutics among patients. Multiple strategies are being planned to determine the future potential of miRNAs to treat a disease. This review embodies the recent work done in the field of miRNA and its role in cardiovascular disease as diagnostic biomarker as well as therapeutic agents. In addition the review highlights the future of miRNAs as a potential therapeutic target and need of designing micronome that may reveal potential predictive targets of miRNA-mRNA interaction.

摘要

心血管疾病(CVD)是全球范围内导致死亡和发病的主要原因。据报道,这种疾病具有慢性性质,其症状在很长一段时间内会逐渐恶化。尽管在 CVD 的治疗方面取得了显著的成就,但现有的药物存在各种不良因素,包括药物毒性、复杂性、耐药性等。RNA 的多功能性使其成为许多人类疾病的重要治疗候选物。深入了解 RNA 生物学,探索具有治疗潜力的新类别的 RNA 将有助于其成功转化为临床应用。了解各种 RNA(如 miRNA、RNA 结合蛋白和 siRNA)在 CVD 中的作用机制将有助于改善患者的治疗效果。目前正在计划采用多种策略来确定 miRNA 治疗疾病的未来潜力。这篇综述体现了 miRNA 及其在心血管疾病中作为诊断生物标志物和治疗剂的作用的最新研究进展。此外,该综述还强调了 miRNA 作为潜在治疗靶点的未来以及设计可能揭示 miRNA-mRNA 相互作用潜在预测靶点的微基因组的必要性。

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