{"title":"GSDMD-mediated pyroptosis: molecular mechanisms, diseases and therapeutic targets.","authors":"Yujuan Li, Bin Guo","doi":"10.1186/s43556-025-00249-8","DOIUrl":null,"url":null,"abstract":"<p><p>Pyroptosis is a regulated form of inflammatory cell death in which Gasdermin D (GSDMD) plays a central role as the key effector molecule. GSDMD-mediated pyroptosis is characterized by complex biological features and considerable heterogeneity in its expression, mechanisms, and functional outcomes across various tissues, cell types, and pathological microenvironments. This heterogeneity is particularly pronounced in inflammation-related diseases and tumors. In the context of inflammatory diseases, GSDMD expression is typically upregulated, and its activation in macrophages, neutrophils, T cells, epithelial cells, and mitochondria triggers both pyroptotic and non-pyroptotic pathways, leading to the release of pro-inflammatory cytokines and exacerbation of tissue damage. However, under certain conditions, GSDMD-mediated pyroptosis may also serve a protective immune function. The expression of GSDMD in tumors is regulated in a more complex manner, where it can either promote immune evasion or, in some instances, induce tumor cell death. As our understanding of GSDMD's role continues to progress, there have been advancements in the development of inhibitors targeting GSDMD-mediated pyroptosis; however, these therapeutic interventions remain in the preclinical phase. This review systematically examines the cellular and molecular complexities of GSDMD-mediated pyroptosis, with a particular emphasis on its roles in inflammation-related diseases and cancer. Furthermore, it underscores the substantial therapeutic potential of GSDMD as a target for precision medicine, highlighting its promising clinical applications.</p>","PeriodicalId":74218,"journal":{"name":"Molecular biomedicine","volume":"6 1","pages":"11"},"PeriodicalIF":6.3000,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11850691/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular biomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s43556-025-00249-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Pyroptosis is a regulated form of inflammatory cell death in which Gasdermin D (GSDMD) plays a central role as the key effector molecule. GSDMD-mediated pyroptosis is characterized by complex biological features and considerable heterogeneity in its expression, mechanisms, and functional outcomes across various tissues, cell types, and pathological microenvironments. This heterogeneity is particularly pronounced in inflammation-related diseases and tumors. In the context of inflammatory diseases, GSDMD expression is typically upregulated, and its activation in macrophages, neutrophils, T cells, epithelial cells, and mitochondria triggers both pyroptotic and non-pyroptotic pathways, leading to the release of pro-inflammatory cytokines and exacerbation of tissue damage. However, under certain conditions, GSDMD-mediated pyroptosis may also serve a protective immune function. The expression of GSDMD in tumors is regulated in a more complex manner, where it can either promote immune evasion or, in some instances, induce tumor cell death. As our understanding of GSDMD's role continues to progress, there have been advancements in the development of inhibitors targeting GSDMD-mediated pyroptosis; however, these therapeutic interventions remain in the preclinical phase. This review systematically examines the cellular and molecular complexities of GSDMD-mediated pyroptosis, with a particular emphasis on its roles in inflammation-related diseases and cancer. Furthermore, it underscores the substantial therapeutic potential of GSDMD as a target for precision medicine, highlighting its promising clinical applications.
焦亡是一种受调控的炎症细胞死亡形式,其中Gasdermin D (GSDMD)作为关键效应分子起着核心作用。gsdmd介导的焦亡具有复杂的生物学特征,其在不同组织、细胞类型和病理微环境中的表达、机制和功能结局具有相当大的异质性。这种异质性在炎症相关疾病和肿瘤中尤为明显。在炎症性疾病的背景下,GSDMD的表达通常上调,其在巨噬细胞、中性粒细胞、T细胞、上皮细胞和线粒体中的激活触发热亡和非热亡途径,导致促炎细胞因子的释放和组织损伤的加剧。然而,在一定条件下,gsdmd介导的焦亡也可能具有保护性免疫功能。GSDMD在肿瘤中的表达以一种更复杂的方式受到调节,它可以促进免疫逃避,或者在某些情况下诱导肿瘤细胞死亡。随着我们对GSDMD作用的理解不断深入,针对GSDMD介导的焦亡的抑制剂的开发也取得了进展;然而,这些治疗干预仍处于临床前阶段。本文系统地研究了gsdmd介导的焦亡的细胞和分子复杂性,特别强调了它在炎症相关疾病和癌症中的作用。此外,它强调了GSDMD作为精准医学靶点的巨大治疗潜力,突出了其具有广阔的临床应用前景。