Department of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
Department of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
Pharmacol Ther. 2023 Nov;251:108545. doi: 10.1016/j.pharmthera.2023.108545. Epub 2023 Oct 21.
More than a decade ago IL-1 blockade was suggested as an add-on therapy for the treatment of cancer. This proposal was based on the overall safety record of anti-IL-1 biologics and the anti-tumor properties of IL-1 blockade in animal models of cancer. Today, a new frontier in IL-1 activity regulation has developed with several orally active NLRP3 inhibitors currently in clinical trials, including cancer. Despite an increasing body of evidence suggesting a role of NLRP3 and IL-1-mediated inflammation driving cancer initiation, immunosuppression, growth, and metastasis, NLRP3 activation in cancer remains controversial. In this review, we discuss the recent advances in the understanding of NLRP3 activation in cancer. Further, we discuss the current opportunities for NLRP3 inhibition in cancer intervention with novel small molecules.
十多年前,人们提出白细胞介素-1(IL-1)阻断作为癌症治疗的附加疗法。这一建议基于抗 IL-1 生物制剂的总体安全性记录,以及 IL-1 阻断在癌症动物模型中的抗肿瘤特性。如今,随着几种在研的口服活性 NLRP3 抑制剂,IL-1 活性调控领域迎来了新的发展,其中包括癌症。尽管越来越多的证据表明 NLRP3 和 IL-1 介导的炎症在推动癌症的发生、免疫抑制、生长和转移中发挥作用,但 NLRP3 在癌症中的激活仍存在争议。在这篇综述中,我们讨论了对 NLRP3 在癌症中激活的理解的最新进展。此外,我们还讨论了新型小分子抑制 NLRP3 在癌症干预中的当前机遇。