1Department of Biology and Pharmaceutical Botany, Medical University of Gdansk, Gdansk, Poland.
2Department of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland.
Cell Mol Biol Lett. 2019 Dec 9;24:69. doi: 10.1186/s11658-019-0196-3. eCollection 2019.
With the first RNA interference (RNAi) drug (ONPATTRO (patisiran)) on the market, we witness the RNAi therapy field reaching a critical turning point, when further improvements in drug candidate design and delivery pipelines should enable fast delivery of novel life changing treatments to patients. Nevertheless, ignoring parallel development of RNAi dedicated in vitro pharmacological profiling aiming to identify undesirable off-target activity may slow down or halt progress in the RNAi field. Since academic research is currently fueling the RNAi development pipeline with new therapeutic options, the objective of this article is to briefly summarize the basics of RNAi therapy, as well as to discuss how to translate basic research into better understanding of related drug candidate safety profiles early in the process.
随着首款 RNA 干扰 (RNAi) 药物(ONPATTRO(patisiran))上市,我们见证了 RNAi 治疗领域正处于一个关键的转折点,此时候选药物设计和输送管道的进一步改进,应该能够为患者快速提供新颖的改变生活的治疗方法。然而,如果忽视 RNAi 专用的体外药理学分析的平行发展,以确定不理想的脱靶活性,可能会减缓或阻碍 RNAi 领域的进展。由于学术研究目前正在为 RNAi 开发管道提供新的治疗选择,本文的目的是简要总结 RNAi 治疗的基础知识,并讨论如何在早期过程中,将基础研究转化为更好地理解相关候选药物的安全性概况。