Institute for Cancer Research, Department of Immunology, Molecular Medicine Group, Montebello, Oslo, Norway.
N Biotechnol. 2010 Jul 31;27(3):236-42. doi: 10.1016/j.nbt.2010.02.015. Epub 2010 Feb 26.
Since its discovery in the late 1990s by Fire and Mello, RNA interference (RNAi) has proven a useful tool for scientists working in the fields of functional genomics, biotechnology, and therapeutic development. However, one of the obstacles of making small interfering RNAs (siRNAs), the main effector of RNAi, a therapeutic agent includes the activation of the immune system, off-target effects, and competition with endogenous microRNAs (miRNAs) for cellular miRNA-processing machinery. Therefore, the translation of RNAi technology into the clinic depends on the development of new strategies to surmount siRNA unwanted effects and identify siRNA sensing receptors as well as to understand the extend of the competition between exogenous and endogenous miRNAs. This minireview summarizes our current knowledge of siRNA sensing by the immune receptors and how to separate siRNA unwanted effects from gene silencing.
自上世纪 90 年代 Fire 和 Mello 发现 RNA 干扰 (RNAi) 以来,它已被证明是功能基因组学、生物技术和治疗开发领域的科学家的有用工具。然而,将小干扰 RNA(siRNA) 作为 RNAi 的主要效应物用于治疗时,其中一个障碍是免疫系统的激活、脱靶效应以及与内源性 microRNA(miRNA) 竞争细胞 miRNA 加工机制。因此,RNAi 技术向临床的转化取决于开发新策略以克服 siRNA 的不良作用,鉴定 siRNA 感应受体,以及了解外源性和内源性 miRNA 之间竞争的程度。这篇综述总结了我们目前对免疫受体识别 siRNA 的认识,以及如何将 siRNA 的不良作用与基因沉默区分开来。