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RNA 药物和小分子的 RNA 靶点:原理、进展与挑战。

RNA Drugs and RNA Targets for Small Molecules: Principles, Progress, and Challenges.

机构信息

Department of Biochemistry and Molecular Medicine, UC Davis School of Medicine, Sacramento, California (A.-M.Y., Y.H.C., M.-J.T.) and College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Goyang-si, Gyonggi-do, Republic of Korea (Y.H.C.)

Department of Biochemistry and Molecular Medicine, UC Davis School of Medicine, Sacramento, California (A.-M.Y., Y.H.C., M.-J.T.) and College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Goyang-si, Gyonggi-do, Republic of Korea (Y.H.C.).

出版信息

Pharmacol Rev. 2020 Oct;72(4):862-898. doi: 10.1124/pr.120.019554.

Abstract

RNA-based therapies, including RNA molecules as drugs and RNA-targeted small molecules, offer unique opportunities to expand the range of therapeutic targets. Various forms of RNAs may be used to selectively act on proteins, transcripts, and genes that cannot be targeted by conventional small molecules or proteins. Although development of RNA drugs faces unparalleled challenges, many strategies have been developed to improve RNA metabolic stability and intracellular delivery. A number of RNA drugs have been approved for medical use, including aptamers (e.g., pegaptanib) that mechanistically act on protein target and small interfering RNAs (e.g., patisiran and givosiran) and antisense oligonucleotides (e.g., inotersen and golodirsen) that directly interfere with RNA targets. Furthermore, guide RNAs are essential components of novel gene editing modalities, and mRNA therapeutics are under development for protein replacement therapy or vaccination, including those against unprecedented severe acute respiratory syndrome coronavirus pandemic. Moreover, functional RNAs or RNA motifs are highly structured to form binding pockets or clefts that are accessible by small molecules. Many natural, semisynthetic, or synthetic antibiotics (e.g., aminoglycosides, tetracyclines, macrolides, oxazolidinones, and phenicols) can directly bind to ribosomal RNAs to achieve the inhibition of bacterial infections. Therefore, there is growing interest in developing RNA-targeted small-molecule drugs amenable to oral administration, and some (e.g., risdiplam and branaplam) have entered clinical trials. Here, we review the pharmacology of novel RNA drugs and RNA-targeted small-molecule medications, with a focus on recent progresses and strategies. Challenges in the development of novel druggable RNA entities and identification of viable RNA targets and selective small-molecule binders are discussed. SIGNIFICANCE STATEMENT: With the understanding of RNA functions and critical roles in diseases, as well as the development of RNA-related technologies, there is growing interest in developing novel RNA-based therapeutics. This comprehensive review presents pharmacology of both RNA drugs and RNA-targeted small-molecule medications, focusing on novel mechanisms of action, the most recent progress, and existing challenges.

摘要

基于 RNA 的疗法,包括作为药物的 RNA 分子和针对 RNA 的小分子,为扩大治疗靶点的范围提供了独特的机会。各种形式的 RNA 可用于选择性地作用于蛋白质、转录本和基因,这些靶点不能被传统的小分子或蛋白质靶向。尽管 RNA 药物的开发面临前所未有的挑战,但已经开发出许多策略来提高 RNA 的代谢稳定性和细胞内递送。一些 RNA 药物已被批准用于医疗用途,包括作用于蛋白质靶标的适体(例如,pegaptanib)和小干扰 RNA(例如,patisiran 和 givosiran)以及反义寡核苷酸(例如,inotersen 和 golodirsen),它们直接干扰 RNA 靶标。此外,向导 RNA 是新型基因编辑模式的重要组成部分,正在开发用于蛋白质替代疗法或疫苗接种的 mRNA 疗法,包括针对前所未有的严重急性呼吸系统综合征冠状病毒大流行的疫苗接种。此外,功能性 RNA 或 RNA 基序高度结构化,形成可被小分子进入的结合口袋或裂缝。许多天然、半合成或合成抗生素(例如,氨基糖苷类、四环素类、大环内酯类、唑烷酮类和苯氧羧酸类)可以直接与核糖体 RNA 结合以抑制细菌感染。因此,人们越来越有兴趣开发可口服的针对 RNA 的小分子药物,其中一些(例如,risdiplam 和 branaplam)已进入临床试验。在这里,我们综述了新型 RNA 药物和针对 RNA 的小分子药物的药理学,重点介绍了最新进展和策略。讨论了新型可成药 RNA 实体的开发以及可行的 RNA 靶标和选择性小分子结合物的鉴定所面临的挑战。意义陈述:随着对 RNA 功能及其在疾病中的关键作用的理解,以及 RNA 相关技术的发展,人们对开发新型基于 RNA 的治疗方法越来越感兴趣。本综述全面介绍了 RNA 药物和针对 RNA 的小分子药物的药理学,重点介绍了新的作用机制、最新进展和现有挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b042/7495341/e300a8e03b26/pr.120.019554absf1.jpg

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