{"title":"异丙酚通过阻断NF-κB/LGI4反馈回路的形成,激活TP53自转录,从而抑制胶质瘤的生长。","authors":"Zhi Wang , Li-na Zhang , Ting Wu , Xu Pan , Le Li","doi":"10.1016/j.tranon.2025.102578","DOIUrl":null,"url":null,"abstract":"<div><div>Accumulating evidence has clarified the anti-cancer function of propofol (PPF) in glioma. However, the underlying regulatory mechanism still remains not fully understood. Our current study screens out a novel gene-leucine-rich glioma-inactivated 4 (LGI4), as a target molecule of PPF, and shows that 10 μg/ml of PPF (a clinically relevant concentration commonly used in multiple previous studies) suppresses the NF-κB signaling pathway to inhibit LGI4 transcription in glioma cells. Clinically, the expression of LGI4 is upregulated in glioma tissues, and its high expression correlates with unfavorable prognosis. Functionally and mechanically, LGI4 promotes tumor growth through blocking TP53 self-transcription by binding to p53 and hindering its nuclear import. Significantly, LGI4 is not only transcriptionally activated by the NF-κB signaling pathway but also feedback activates NF-κB signaling by inhibiting the interaction of IKIP with the IKKα/IKKβ/NEMO complex. Importantly, PPF treatment can break this positive feedback loop. Collectively, our findings uncover that PPF upregulates p53 expression by disrupting the NF-κB/LGI4 feedback loop, thereby inhibiting glioma growth, highlighting it is a potential therapeutic target for future glioma treatment.</div></div>","PeriodicalId":48975,"journal":{"name":"Translational Oncology","volume":"62 ","pages":"Article 102578"},"PeriodicalIF":5.0000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Propofol inhibits glioma growth by blocking the formation of the NF-κB/LGI4 feedback loop to activate TP53 self-transcription\",\"authors\":\"Zhi Wang , Li-na Zhang , Ting Wu , Xu Pan , Le Li\",\"doi\":\"10.1016/j.tranon.2025.102578\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Accumulating evidence has clarified the anti-cancer function of propofol (PPF) in glioma. However, the underlying regulatory mechanism still remains not fully understood. Our current study screens out a novel gene-leucine-rich glioma-inactivated 4 (LGI4), as a target molecule of PPF, and shows that 10 μg/ml of PPF (a clinically relevant concentration commonly used in multiple previous studies) suppresses the NF-κB signaling pathway to inhibit LGI4 transcription in glioma cells. Clinically, the expression of LGI4 is upregulated in glioma tissues, and its high expression correlates with unfavorable prognosis. Functionally and mechanically, LGI4 promotes tumor growth through blocking TP53 self-transcription by binding to p53 and hindering its nuclear import. Significantly, LGI4 is not only transcriptionally activated by the NF-κB signaling pathway but also feedback activates NF-κB signaling by inhibiting the interaction of IKIP with the IKKα/IKKβ/NEMO complex. Importantly, PPF treatment can break this positive feedback loop. Collectively, our findings uncover that PPF upregulates p53 expression by disrupting the NF-κB/LGI4 feedback loop, thereby inhibiting glioma growth, highlighting it is a potential therapeutic target for future glioma treatment.</div></div>\",\"PeriodicalId\":48975,\"journal\":{\"name\":\"Translational Oncology\",\"volume\":\"62 \",\"pages\":\"Article 102578\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1936523325003092\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Oncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1936523325003092","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
Propofol inhibits glioma growth by blocking the formation of the NF-κB/LGI4 feedback loop to activate TP53 self-transcription
Accumulating evidence has clarified the anti-cancer function of propofol (PPF) in glioma. However, the underlying regulatory mechanism still remains not fully understood. Our current study screens out a novel gene-leucine-rich glioma-inactivated 4 (LGI4), as a target molecule of PPF, and shows that 10 μg/ml of PPF (a clinically relevant concentration commonly used in multiple previous studies) suppresses the NF-κB signaling pathway to inhibit LGI4 transcription in glioma cells. Clinically, the expression of LGI4 is upregulated in glioma tissues, and its high expression correlates with unfavorable prognosis. Functionally and mechanically, LGI4 promotes tumor growth through blocking TP53 self-transcription by binding to p53 and hindering its nuclear import. Significantly, LGI4 is not only transcriptionally activated by the NF-κB signaling pathway but also feedback activates NF-κB signaling by inhibiting the interaction of IKIP with the IKKα/IKKβ/NEMO complex. Importantly, PPF treatment can break this positive feedback loop. Collectively, our findings uncover that PPF upregulates p53 expression by disrupting the NF-κB/LGI4 feedback loop, thereby inhibiting glioma growth, highlighting it is a potential therapeutic target for future glioma treatment.
期刊介绍:
Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.