{"title":"Juglone induces GSDME-mediated pyroptosis by targeting HSP90α ATPase domain to promote STAT3 degradation in glioblastoma multiforme.","authors":"Hao-Di Wu, Shuai Chen, Jia-Wen Li, Liu-Tao Ma, Jia-Nan Ma, Yong-Ang Li, Ye Xiong, Yu-Jia Yang, Shi-Hao Chen, Jia-Yi Chen, Xue Wang, Peng Wang","doi":"10.1016/j.taap.2026.118070","DOIUrl":null,"url":null,"abstract":"<p><p>Glioblastoma (GBM) is a highly aggressive primary brain tumor with grim overall median survival, and its therapeutic efficacy is severely limited due to drug resistance. Therefore, developing effective and safe chemotherapy regimens is urgently required. Juglone, a natural bioactive constituent derived from traditional Chinese herbs, has emerged as a promising therapeutic agent against various human malignancies. However, the direct molecular target and the mechanisms against GBM remain poorly defined. Herein, we demonstrated that juglone exhibited anti-GBM activity both in vitro and in vivo by selectively inducing GSDME-mediated pyroptosis, but not canonical GSDMD-mediated pyroptosis. Genetic ablation of GSDME or pharmacological inhibition of caspase-3 significantly abolished juglone-elicited pyroptotic cell death. Mechanistically, juglone induced mitochondrial fission and subsequent mtROS production, which constituted a positive regulatory loop to initiate caspase-3/GSDME-mediated pyroptosis. Furthermore, combining network pharmacology, ATPase activity assay, cellular thermal shift assay (CETSA), and co-immunoprecipitation, we identified HSP90α as a direct binding target of juglone, with the binding interface localized to the ATP-binding pocket of HSP90α. Further mechanistic analysis revealed that juglone disrupted the HSP90α-STAT3 interaction, facilitating ubiquitin-proteasome-dependent STAT3 degradation and concurrently elevating oxidative stress. In summary, our study uncovered a regulatory axis linking juglone to the HSP90α/STAT3 signaling, which governs mtROS-driven pyroptosis in GBM cells. As a novel HSP90α ATPase inhibitor, juglone represents a promising natural therapeutic candidate for GBM intervention.</p>","PeriodicalId":23174,"journal":{"name":"Toxicology and applied pharmacology","volume":" ","pages":"118070"},"PeriodicalIF":3.6000,"publicationDate":"2026-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicology and applied pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.taap.2026.118070","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Glioblastoma (GBM) is a highly aggressive primary brain tumor with grim overall median survival, and its therapeutic efficacy is severely limited due to drug resistance. Therefore, developing effective and safe chemotherapy regimens is urgently required. Juglone, a natural bioactive constituent derived from traditional Chinese herbs, has emerged as a promising therapeutic agent against various human malignancies. However, the direct molecular target and the mechanisms against GBM remain poorly defined. Herein, we demonstrated that juglone exhibited anti-GBM activity both in vitro and in vivo by selectively inducing GSDME-mediated pyroptosis, but not canonical GSDMD-mediated pyroptosis. Genetic ablation of GSDME or pharmacological inhibition of caspase-3 significantly abolished juglone-elicited pyroptotic cell death. Mechanistically, juglone induced mitochondrial fission and subsequent mtROS production, which constituted a positive regulatory loop to initiate caspase-3/GSDME-mediated pyroptosis. Furthermore, combining network pharmacology, ATPase activity assay, cellular thermal shift assay (CETSA), and co-immunoprecipitation, we identified HSP90α as a direct binding target of juglone, with the binding interface localized to the ATP-binding pocket of HSP90α. Further mechanistic analysis revealed that juglone disrupted the HSP90α-STAT3 interaction, facilitating ubiquitin-proteasome-dependent STAT3 degradation and concurrently elevating oxidative stress. In summary, our study uncovered a regulatory axis linking juglone to the HSP90α/STAT3 signaling, which governs mtROS-driven pyroptosis in GBM cells. As a novel HSP90α ATPase inhibitor, juglone represents a promising natural therapeutic candidate for GBM intervention.
期刊介绍:
Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products.
Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged.
Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.