School of Life Science, Advanced Research Institute of Multidisciplinary Science, and Institute of Engineering Medicine, Key Laboratory of Molecular Medicine and Biotherapy, Beijing Institute of Technology, Beijing, China.
Methods Mol Biol. 2021;2282:77-100. doi: 10.1007/978-1-0716-1298-9_6.
Small interfering RNA (siRNA) is a clinically approved therapeutic modality, which has attracted widespread attention not only from basic research but also from pharmaceutical industry. As siRNA can theoretically modulate any disease-related gene's expression, plenty of siRNA therapeutic pipelines have been established by tens of biotechnology companies. The drug performance of siRNA heavily depends on the sequence, the chemical modification, and the delivery of siRNA. Here, we describe the rational design protocol of siRNA, and provide some modification patterns that can enhance siRNA's stability and reduce its off-target effect. Also, the delivery method based on N-acetylgalactosamine (GalNAc)-siRNA conjugate that is widely employed to develop therapeutic regimens for liver-related diseases is also recapitulated.
小干扰 RNA(siRNA)是一种临床认可的治疗方式,不仅引起了基础研究领域的广泛关注,也引起了制药行业的广泛关注。由于 siRNA 理论上可以调节任何与疾病相关的基因表达,因此数十家生物技术公司已经建立了大量的 siRNA 治疗管线。siRNA 的药物性能很大程度上取决于 siRNA 的序列、化学修饰和递送。在这里,我们描述了 siRNA 的合理设计方案,并提供了一些可以增强 siRNA 稳定性和降低其脱靶效应的修饰模式。此外,还概括了基于 N-乙酰半乳糖胺(GalNAc)-siRNA 缀合物的递送方法,该方法广泛用于开发针对肝脏相关疾病的治疗方案。