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NLRP3 和焦亡抑制剂治疗炎症性疾病。

NLRP3 and pyroptosis blockers for treating inflammatory diseases.

机构信息

The Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast BT9 7BL, UK.

Institute for Molecular Bioscience and IMB Centre for Inflammation and Disease Research, The University of Queensland, QLD 4072, Australia.

出版信息

Trends Pharmacol Sci. 2022 Aug;43(8):653-668. doi: 10.1016/j.tips.2022.04.003. Epub 2022 May 3.

Abstract

The nucleotide-binding oligomerization domain, leucine-rich repeat and pyrin domain-containing protein 3 (NLRP3) inflammasome has emerged as a key mediator of pathological inflammation in many diseases and is an exciting drug target. Here, we review the molecular basis of NLRP3 inhibition by drug-like small molecules under development as novel therapeutics. We also summarize recent strategies to block pyroptosis as a novel approach to suppress chronic inflammation. Major recent developments in this area include the elucidation of mechanisms of action (MoAs) by which small molecules block NLRP3 inflammasome assembly and gasdermin D (GSDMD)-induced pyroptosis. We also discuss the status of clinical trials using agents that block specific components of the NLRP3 pathway, including their potential clinical applications for the treatment of many diseases.

摘要

核苷酸结合寡聚化结构域、富含亮氨酸重复序列和吡咯烷结构域蛋白 3(NLRP3)炎性小体已成为许多疾病中病理性炎症的关键介质,也是一个令人兴奋的药物靶点。在这里,我们综述了处于开发阶段的类药小分子抑制 NLRP3 的分子基础,这些小分子可能成为新型治疗药物。我们还总结了最近阻止细胞焦亡的策略,这是抑制慢性炎症的一种新方法。该领域的主要新进展包括阐明小分子抑制 NLRP3 炎性小体组装和gasdermin D(GSDMD)诱导的细胞焦亡的作用机制(MoA)。我们还讨论了使用阻断 NLRP3 通路特定成分的药物进行临床试验的现状,包括它们在治疗许多疾病方面的潜在临床应用。

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