Graduate School of Medical Science and Engineering, Korea Advanced Institute for Science and Technology (KAIST), Daejeon, Republic of Korea.
BioMedical Research Center, KAIST, Daejeon, Republic of Korea.
Exp Mol Med. 2023 Jul;55(7):1283-1292. doi: 10.1038/s12276-023-00998-y. Epub 2023 Jul 10.
RNA interference mediated by small interfering RNAs (siRNAs) has been exploited for the development of therapeutics. siRNAs can be a powerful therapeutic tool because the working mechanisms of siRNAs are straightforward. siRNAs determine targets based on their sequence and specifically regulate the gene expression of the target gene. However, efficient delivery of siRNAs to the target organ has long been an issue that needs to be solved. Tremendous efforts regarding siRNA delivery have led to significant progress in siRNA drug development, and from 2018 to 2022, a total of five siRNA drugs were approved for the treatment of patients. Although all FDA-approved siRNA drugs target the hepatocytes of the liver, siRNA-based drugs targeting different organs are in clinical trials. In this review, we introduce siRNA drugs in the market and siRNA drug candidates in clinical trials that target cells in multiple organs. The liver, eye, and skin are the preferred organs targeted by siRNAs. Three or more siRNA drug candidates are in phase 2 or 3 clinical trials to suppress gene expression in these preferred organs. On the other hand, the lungs, kidneys, and brain are challenging organs with relatively few clinical trials. We discuss the characteristics of each organ related to the advantages and disadvantages of siRNA drug targeting and strategies to overcome the barriers in delivering siRNAs based on organ-specific siRNA drugs that have progressed to clinical trials.
小干扰 RNA(siRNA)介导的 RNA 干扰已被用于治疗药物的开发。siRNA 可以成为一种强大的治疗工具,因为 siRNA 的作用机制很简单。siRNA 根据其序列确定靶标,并特异性调节靶基因的基因表达。然而,将 siRNA 有效递送至靶器官一直是一个需要解决的问题。针对 siRNA 递送的巨大努力推动了 siRNA 药物开发的显著进展,从 2018 年到 2022 年,共有 5 种 siRNA 药物被批准用于治疗患者。尽管所有获得 FDA 批准的 siRNA 药物均靶向肝脏的肝细胞,但针对不同器官的基于 siRNA 的药物正在临床试验中。在这篇综述中,我们介绍了市场上的 siRNA 药物和处于临床试验阶段的针对多种器官细胞的 siRNA 药物候选物。肝脏、眼睛和皮肤是 siRNA 首选的靶向器官。有三个或更多的 siRNA 药物候选物处于 2 期或 3 期临床试验中,以抑制这些首选器官中的基因表达。另一方面,肺部、肾脏和大脑是具有相对较少临床试验的具有挑战性的器官。我们讨论了与 siRNA 药物靶向的优缺点相关的每个器官的特征,以及基于已进展到临床试验的针对特定器官的 siRNA 药物来克服基于 siRNA 递送障碍的策略。