Chemical modification of siRNAs for in vivo use.

Mark A Behlke
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引用次数: 451

Abstract

Well over a hundred reports have been published describing use of synthetic small-interfering RNAs (siRNAs) in animals. The majority of these reports employed unmodified RNA duplexes. While unmodified RNA is the natural effector molecule of RNA interference, certain problems arise with experimental or therapeutic use of RNA duplexes in vivo, some of which can be improved or solved through use of chemical modifications. Judicious use of chemical modifications can improve the nuclease stability of an RNA duplex, decrease the likelihood of triggering an innate immune response, lower the incidence of off-target effects (OTEs), and improve pharmacodynamics. This review will examine studies that document the utility of various chemical modifications for use in siRNAs, both in vitro and in vivo, with close attention given to reports demonstrating actual performance in animal model systems.

体内使用sirna的化学修饰。
已经发表了一百多篇报道,描述了在动物身上使用合成的小干扰rna (sirna)。这些报道大多采用未修饰的RNA双链。虽然未经修饰的RNA是RNA干扰的天然效应分子,但在体内实验或治疗中使用RNA双链会出现一些问题,其中一些问题可以通过使用化学修饰来改善或解决。明智地使用化学修饰可以提高RNA双链核酸酶的稳定性,降低触发先天免疫反应的可能性,降低脱靶效应(OTEs)的发生率,并改善药效学。本综述将研究记录各种化学修饰在sirna中使用的效用的研究,包括体外和体内,并密切关注在动物模型系统中证明实际性能的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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