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基于 RNAi 的治疗方法和新型 RNA 生物工程技术。

RNAi-Based Therapeutics and Novel RNA Bioengineering Technologies.

机构信息

Department of Biochemistry and Molecular Medicine, University of California (UC) Davis School of Medicine, Sacramento, California.

Department of Biochemistry and Molecular Medicine, University of California (UC) Davis School of Medicine, Sacramento, California

出版信息

J Pharmacol Exp Ther. 2023 Jan;384(1):133-154. doi: 10.1124/jpet.122.001234. Epub 2022 Jun 9.

Abstract

RNA interference (RNAi) provides researchers with a versatile means to modulate target gene expression. The major forms of RNAi molecules, genome-derived microRNAs (miRNAs) and exogenous small interfering RNAs (siRNAs), converge into RNA-induced silencing complexes to achieve posttranscriptional gene regulation. RNAi has proven to be an adaptable and powerful therapeutic strategy where advancements in chemistry and pharmaceutics continue to bring RNAi-based drugs into the clinic. With four siRNA medications already approved by the US Food and Drug Administration (FDA), several RNAi-based therapeutics continue to advance to clinical trials with functions that closely resemble their endogenous counterparts. Although intended to enhance stability and improve efficacy, chemical modifications may increase risk of off-target effects by altering RNA structure, folding, and biologic activity away from their natural equivalents. Novel technologies in development today seek to use intact cells to yield true biologic RNAi agents that better represent the structures, stabilities, activities, and safety profiles of natural RNA molecules. In this review, we provide an examination of the mechanisms of action of endogenous miRNAs and exogenous siRNAs, the physiologic and pharmacokinetic barriers to therapeutic RNA delivery, and a summary of the chemical modifications and delivery platforms in use. We overview the pharmacology of the four FDA-approved siRNA medications (patisiran, givosiran, lumasiran, and inclisiran) as well as five siRNAs and several miRNA-based therapeutics currently in clinical trials. Furthermore, we discuss the direct expression and stable carrier-based, in vivo production of novel biologic RNAi agents for research and development. SIGNIFICANCE STATEMENT: In our review, we summarize the major concepts of RNA interference (RNAi), molecular mechanisms, and current state and challenges of RNAi drug development. We focus our discussion on the pharmacology of US Food and Drug Administration-approved RNAi medications and those siRNAs and miRNA-based therapeutics that entered the clinical investigations. Novel approaches to producing new true biological RNAi molecules for research and development are highlighted.

摘要

RNA 干扰 (RNAi) 为研究人员提供了一种灵活的方法来调节靶基因表达。RNAi 分子的主要形式,基因组衍生的 microRNAs (miRNAs) 和外源性小干扰 RNA (siRNAs),汇聚到 RNA 诱导的沉默复合物中,以实现转录后基因调控。RNAi 已被证明是一种适应性强且强大的治疗策略,化学和药剂学的进步不断将基于 RNAi 的药物推向临床。美国食品和药物管理局 (FDA) 已经批准了四种 siRNA 药物,几种基于 RNAi 的疗法继续推进临床试验,其功能与内源性药物非常相似。尽管旨在提高稳定性和提高疗效,但通过改变 RNA 结构、折叠和生物活性使其偏离天然等同物,化学修饰可能会增加脱靶效应的风险。目前正在开发的新技术旨在利用完整细胞产生真正的生物 RNAi 制剂,这些制剂更好地代表天然 RNA 分子的结构、稳定性、活性和安全性特征。在这篇综述中,我们检查了内源性 miRNAs 和外源性 siRNAs 的作用机制、治疗性 RNA 递送到体内的生理和药代动力学障碍,以及正在使用的化学修饰和递药平台的概述。我们综述了 FDA 批准的四种 siRNA 药物(patisiran、givosiran、lumasiran 和 inclisiran)以及五种 siRNA 和几种 miRNA 治疗剂的药理学,这些药物目前正在临床试验中。此外,我们讨论了用于研究和开发的新型生物 RNAi 制剂的直接表达和稳定载体的体内生产。

意义

在我们的综述中,我们总结了 RNA 干扰 (RNAi) 的主要概念、分子机制以及 RNAi 药物开发的现状和挑战。我们将讨论重点放在 FDA 批准的 RNAi 药物以及进入临床试验的 siRNA 和 miRNA 治疗剂的药理学上。突出强调了用于研究和开发的新型真生物 RNAi 分子的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f453/9827509/bbc931147d62/jpet.122.001234absf1.jpg

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