Ying Xiaohong, Chen Qiaohui, Yang Yongqi, Wu Ziyu, Zeng Wan, Miao Chenxi, Huang Qiong, Ai Kelong
Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, 410008, China.
Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410013, China.
Mol Cancer. 2024 Dec 23;23(1):277. doi: 10.1186/s12943-024-02186-6.
cGAS-STING pathway stands at the forefront of innate immunity and plays a critical role in regulating adaptive immune responses, making it as a key orchestrator of anti-tumor immunity. Despite the great potential, clinical outcomes with cGAS-STING activators have been disappointing due to their unfavorable in vivo fate, signaling an urgent need for innovative solutions to bridge the gap in clinical translation. Recent advancements in nanotechnology have propelled cGAS-STING-targeting nanomedicines to the cutting-edge of cancer therapy, leveraging precise drug delivery systems and multifunctional platforms to achieve remarkable region-specific biodistribution and potent therapeutic efficacy. In this review, we provide an in-depth exploration of the molecular mechanisms that govern cGAS-STING signaling and its potential to dynamically modulate the anti-tumor immune cycle. We subsequently introduced several investigational cGAS-STING-dependent anti-tumor agents and summarized their clinical trial progress. Additionally, we provided a comprehensive review of the unique advantages of cGAS-STING-targeted nanomedicines, highlighting the transformative potential of nanotechnology in this field. Furthermore, we comprehensively reviewed and comparatively analyzed the latest breakthroughs cGAS-STING-targeting nanomedicine, focusing on strategies that induce cytosolic DNA generation via exogenous DNA delivery, chemotherapy, radiotherapy, or dynamic therapies, as well as the nanodelivery of STING agonists. Lastly, we discuss the future prospects and challenges in cGAS-STING-targeting nanomedicine development, offering new insights to bridge the gap between mechanistic research and drug development, thereby opening new pathways in cancer treatment.
环鸟苷酸-腺苷酸合成酶-干扰素基因刺激蛋白(cGAS-STING)通路处于固有免疫的前沿,在调节适应性免疫反应中发挥关键作用,使其成为抗肿瘤免疫的关键协调者。尽管具有巨大潜力,但由于cGAS-STING激活剂在体内的不良命运,其临床结果一直令人失望,这表明迫切需要创新解决方案来弥合临床转化中的差距。纳米技术的最新进展已将靶向cGAS-STING的纳米药物推向癌症治疗的前沿,利用精确的药物递送系统和多功能平台实现显著的区域特异性生物分布和强大的治疗效果。在这篇综述中,我们深入探讨了调控cGAS-STING信号传导的分子机制及其动态调节抗肿瘤免疫周期的潜力。随后,我们介绍了几种正在研究的依赖cGAS-STING的抗肿瘤药物,并总结了它们的临床试验进展。此外,我们全面回顾了靶向cGAS-STING的纳米药物的独特优势,强调了纳米技术在该领域的变革潜力。此外,我们全面回顾并比较分析了靶向cGAS-STING的纳米药物的最新突破,重点关注通过外源性DNA递送、化疗、放疗或动态疗法诱导胞质DNA生成的策略,以及STING激动剂的纳米递送。最后,我们讨论了靶向cGAS-STING的纳米药物开发的未来前景和挑战,为弥合机制研究与药物开发之间的差距提供新见解,从而为癌症治疗开辟新途径。