Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia.
Methods Mol Biol. 2020;2115:57-77. doi: 10.1007/978-1-0716-0290-4_3.
RNA interference (RNAi) is a powerful tool for suppressing gene expression associated with various diseases that are not amenable to treatment with low molecular weight drugs. Despite significant progress in this area, the potential for therapeutic use of RNAi in humans is limited due to the lack of efficient delivery systems. Bioconjugation is one of the most promising methods for delivering siRNA to cells and tissues, since conjugation of siRNA with molecules capable of penetrating cells through natural transport mechanisms can provide specificity of delivery without toxic effects and unwanted immunostimulation. Here we describe the design, preparation, and in vivo evaluation of cholesterol-containing siRNA conjugates able to accumulate in the tumor, penetrate into cells without a carrier, and suppress the expression of the target genes.
RNA 干扰 (RNAi) 是一种强大的工具,可用于抑制与无法用小分子药物治疗的各种疾病相关的基因表达。尽管在这一领域取得了重大进展,但由于缺乏有效的递药系统,RNAi 在人类中的治疗应用潜力受到限制。生物共轭是将 siRNA 递送到细胞和组织的最有前途的方法之一,因为将 siRNA 与能够通过天然转运机制穿透细胞的分子共轭可以提供递送的特异性,而没有毒性作用和不必要的免疫刺激。在这里,我们描述了能够在肿瘤中积累、无需载体即可穿透细胞并抑制靶基因表达的含胆固醇 siRNA 缀合物的设计、制备和体内评价。