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RNA 治疗学的创新发展与新兴技术。

Innovative developments and emerging technologies in RNA therapeutics.

机构信息

Department of Paediatrics, Medical Sciences Division, University of Oxford, Oxford, UK.

Oligonucleotide Chemistry, Discovery Sciences, BioPharmaceuticals R&d, AstraZeneca, Gothenburg, Sweden.

出版信息

RNA Biol. 2022;19(1):313-332. doi: 10.1080/15476286.2022.2027150. Epub 2021 Dec 31.

Abstract

RNA-based therapeutics are emerging as a powerful platform for the treatment of multiple diseases. Currently, the two main categories of nucleic acid therapeutics, antisense oligonucleotides and small interfering RNAs (siRNAs), achieve their therapeutic effect through either gene silencing, splicing modulation or microRNA binding, giving rise to versatile options to target pathogenic gene expression patterns. Moreover, ongoing research seeks to expand the scope of RNA-based drugs to include more complex nucleic acid templates, such as messenger RNA, as exemplified by the first approved mRNA-based vaccine in 2020. The increasing number of approved sequences and ongoing clinical trials has attracted considerable interest in the chemical development of oligonucleotides and nucleic acids as drugs, especially since the FDA approval of the first siRNA drug in 2018. As a result, a variety of innovative approaches is emerging, highlighting the potential of RNA as one of the most prominent therapeutic tools in the drug design and development pipeline. This review seeks to provide a comprehensive summary of current efforts in academia and industry aimed at fully realizing the potential of RNA-based therapeutics. Towards this, we introduce established and emerging RNA-based technologies, with a focus on their potential as biosensors and therapeutics. We then describe their mechanisms of action and their application in different disease contexts, along with the strengths and limitations of each strategy. Since the nucleic acid toolbox is rapidly expanding, we also introduce RNA minimal architectures, RNA/protein cleavers and viral RNA as promising modalities for new therapeutics and discuss future directions for the field.

摘要

RNA 疗法作为治疗多种疾病的强大平台正在兴起。目前,核酸疗法的两个主要类别,反义寡核苷酸和小干扰 RNA(siRNA),通过基因沉默、剪接调节或 microRNA 结合来实现其治疗效果,从而为靶向致病基因表达模式提供了多种选择。此外,正在进行的研究旨在将 RNA 药物的范围扩大到包括更复杂的核酸模板,如信使 RNA,正如 2020 年首个批准的基于 mRNA 的疫苗所证明的那样。越来越多的已批准序列和正在进行的临床试验引起了人们对寡核苷酸和核酸作为药物的化学开发的极大兴趣,尤其是自 2018 年 FDA 批准首个 siRNA 药物以来。因此,各种创新方法正在涌现,突显了 RNA 作为药物设计和开发管道中最突出的治疗工具之一的潜力。本综述旨在全面总结学术界和工业界目前为充分实现 RNA 疗法潜力所做的努力。为此,我们介绍了已建立和新兴的 RNA 技术,重点介绍它们作为生物传感器和疗法的潜力。然后,我们描述了它们的作用机制及其在不同疾病背景下的应用,以及每种策略的优缺点。由于核酸工具箱正在迅速扩展,我们还介绍了 RNA 最小架构、RNA/蛋白质切割剂和病毒 RNA 作为新疗法的有前途的模式,并讨论了该领域的未来方向。

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