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小药物,大影响:反义寡核苷酸在研究和药物开发中的非凡影响。

Small Drugs, Huge Impact: The Extraordinary Impact of Antisense Oligonucleotides in Research and Drug Development.

机构信息

University Rennes, CNRS, IGDR (Institute of Genetics and Development of Rennes)-UMR 6290, F-35000 Rennes, France.

Department of Oncology, University of Turin, 10124 Turin, Italy.

出版信息

Molecules. 2022 Jan 15;27(2):536. doi: 10.3390/molecules27020536.

Abstract

Antisense oligonucleotides (ASOs) are an increasingly represented class of drugs. These small sequences of nucleotides are designed to precisely target other oligonucleotides, usually RNA species, and are modified to protect them from degradation by nucleases. Their specificity is due to their sequence, so it is possible to target any RNA sequence that is already known. These molecules are very versatile and adaptable given that their sequence and chemistry can be custom manufactured. Based on the chemistry being used, their activity may significantly change and their effects on cell function and phenotypes can differ dramatically. While some will cause the target RNA to decay, others will only bind to the target and act as a steric blocker. Their incredible versatility is the key to manipulating several aspects of nucleic acid function as well as their process, and alter the transcriptome profile of a specific cell type or tissue. For example, they can be used to modify splicing or mask specific sites on a target. The entire design rather than just the sequence is essential to ensuring the specificity of the ASO to its target. Thus, it is vitally important to ensure that the complete process of drug design and testing is taken into account. ASOs' adaptability is a considerable advantage, and over the past decades has allowed multiple new drugs to be approved. This, in turn, has had a significant and positive impact on patient lives. Given current challenges presented by the COVID-19 pandemic, it is necessary to find new therapeutic strategies that would complement the vaccination efforts being used across the globe. ASOs may be a very powerful tool that can be used to target the virus RNA and provide a therapeutic paradigm. The proof of the efficacy of ASOs as an anti-viral agent is long-standing, yet no molecule currently has FDA approval. The emergence and widespread use of RNA vaccines during this health crisis might provide an ideal opportunity to develop the first anti-viral ASOs on the market. In this review, we describe the story of ASOs, the different characteristics of their chemistry, and how their characteristics translate into research and as a clinical tool.

摘要

反义寡核苷酸 (ASO) 是一类日益受到关注的药物。这些核苷酸的小序列旨在精确靶向其他寡核苷酸,通常是 RNA 种类,并经过修饰以防止被核酸酶降解。它们的特异性源于其序列,因此可以靶向任何已知的 RNA 序列。这些分子非常灵活多变,因为它们的序列和化学性质可以定制。基于所用的化学物质,它们的活性可能会发生显著变化,并且它们对细胞功能和表型的影响可能会有很大差异。有些会导致靶 RNA 降解,而有些则仅与靶标结合并充当空间位阻阻断剂。其令人难以置信的多功能性是操纵核酸功能及其过程的关键,并改变特定细胞类型或组织的转录组特征。例如,它们可用于修饰剪接或屏蔽靶标上的特定位点。整个设计而不仅仅是序列对于确保 ASO 对其靶标的特异性至关重要。因此,必须确保药物设计和测试的整个过程都得到考虑。ASO 的适应性是一个相当大的优势,在过去的几十年中,已经有多种新药获得批准。这反过来又对患者的生活产生了重大而积极的影响。鉴于当前 COVID-19 大流行带来的挑战,有必要寻找新的治疗策略,以补充全球正在使用的疫苗接种工作。ASO 可能是一种非常强大的工具,可以用于靶向病毒 RNA 并提供治疗范例。ASO 作为抗病毒剂的功效早已得到证实,但目前没有一种分子获得 FDA 批准。在这场健康危机期间,RNA 疫苗的出现和广泛使用可能为开发市场上第一种抗病毒 ASO 提供了绝佳机会。在这篇综述中,我们描述了 ASO 的故事、它们化学性质的不同特征,以及它们的特征如何转化为研究和临床工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e81/8781596/e8206b508caf/molecules-27-00536-g001.jpg

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