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小干扰RNA与短发夹RNA:异同点

siRNA vs. shRNA: similarities and differences.

作者信息

Rao Donald D, Vorhies John S, Senzer Neil, Nemunaitis John

机构信息

Gradalis, Inc., Dallas, TX, USA.

出版信息

Adv Drug Deliv Rev. 2009 Jul 25;61(9):746-59. doi: 10.1016/j.addr.2009.04.004. Epub 2009 Apr 20.

Abstract

RNA interference (RNAi) is a natural process through which expression of a targeted gene can be knocked down with high specificity and selectivity. Using available technology and bioinformatics investigators will soon be able to identify relevant bio molecular tumor network hubs as potential key targets for knockdown approaches. Methods of mediating the RNAi effect involve small interfering RNA (siRNA), short hairpin RNA (shRNA) and bi-functional shRNA. The simplicity of siRNA manufacturing and transient nature of the effect per dose are optimally suited for certain medical disorders (i.e. viral injections). However, using the endogenous processing machinery, optimized shRNA constructs allow for high potency and sustainable effects using low copy numbers resulting in less off-target effects, particularly if embedded in a miRNA scaffold. Bi-functional design may further enhance potency and safety of RNAi-based therapeutics. Remaining challenges include tumor selective delivery vehicles and more complete evaluation of the scope and scale of off-target effects. This review will compare siRNA, shRNA and bi-functional shRNA.

摘要

RNA干扰(RNAi)是一种自然过程,通过该过程可以高度特异性和选择性地敲低靶向基因的表达。利用现有的技术和生物信息学,研究人员很快就能识别出相关的生物分子肿瘤网络枢纽,作为敲低方法的潜在关键靶点。介导RNAi效应的方法包括小干扰RNA(siRNA)、短发夹RNA(shRNA)和双功能shRNA。siRNA制造的简便性以及每剂量效应的短暂性最适合某些医学病症(如病毒注射)。然而,利用内源性加工机制,优化的shRNA构建体使用低拷贝数就能实现高效力和可持续效应,从而减少脱靶效应,特别是当嵌入miRNA支架时。双功能设计可能会进一步提高基于RNAi的治疗药物的效力和安全性。剩下的挑战包括肿瘤选择性递送载体以及对脱靶效应的范围和规模进行更全面的评估。本综述将比较siRNA、shRNA和双功能shRNA。

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