Guo Jianfeng, Huang Leaf
School of Pharmaceutical Sciences, Jilin University, Changchun 130021, China.
Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC 27599, USA.
Trends Pharmacol Sci. 2022 Nov;43(11):957-972. doi: 10.1016/j.tips.2022.08.006. Epub 2022 Sep 8.
Activation of the cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS)-stimulator of interferon genes (STING) pathway has great potential to promote antitumor immunity. Development of activators for the cGAS-STING pathway (cGAS-STING activators) has profoundly revolutionized tumor immunotherapy. However, successful clinical application of cGAS-STING activators is contingent on having appropriate systems to achieve safe, effective, and specific delivery. There is an increasing emphasis on the design and application of nano drug delivery systems (NDDS) that can facilitate the delivery potential of cGAS-STING activators. In this review, we discuss barriers for translational development of cGAS-STING activators (DNA damaging drugs and STING agonists) and recent advances of NDDS for these agents in tumor immunotherapy.
环磷酸鸟苷-腺苷酸合成酶(cGAS)-干扰素基因刺激因子(STING)通路的激活在促进抗肿瘤免疫方面具有巨大潜力。cGAS-STING通路激活剂(cGAS-STING激活剂)的开发彻底改变了肿瘤免疫治疗。然而,cGAS-STING激活剂的成功临床应用取决于是否有合适的系统来实现安全、有效和特异性递送。人们越来越重视能够促进cGAS-STING激活剂递送潜力的纳米药物递送系统(NDDS)的设计和应用。在这篇综述中,我们讨论了cGAS-STING激活剂(DNA损伤药物和STING激动剂)转化开发的障碍以及这些药物在肿瘤免疫治疗中NDDS的最新进展。