Developing and validating a prognostic disulfidptosis-related signature for glioblastoma: predicting radioresistance and synergestic effect with immunotherapy.

IF 2.7 3区 医学 Q3 ONCOLOGY
Chen Chen, Peixin Tan, Wenqing Feng, Yuan Lei, Shushu Hu, Dehuan Xie, Yantan Liu, Chen Ren, Shasha Du
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引用次数: 0

Abstract

Background: Programmed cell death (PCD) modulated radioresistance is one of the predominant causes of treatment failure in glioblastoma (GBM). Disulfidptosis, a newly discovered form of PCD, plays a crucial role in GBM progression. However, the association among disulfidptosis, radiosensitivity and radiotherapy (RT) in GBM remain unclear.

Methods: We systematically analyzed disulfidptosis-related genes in 1075 GBM patients and constructed a disulfidptosis-related gene signature (DRS). Correlations among the DRS, patient prognosis and immune microenvironment were fully explored. The effects of DRS and EFEMP2 on radiotherapy efficacy were investigated via single cell sequencing analysis and validated via in vitro and in vivo experiments.

Results: The DRS was identified as a robust and independent prognostic biomarker for GBM by multivariate Cox regression analysis, receiver operating characteristic (ROC) curve analysis and decision curve analysis (DCA) in multiple cohorts. High DRS is characterized by radioresistance, and EFEMP2 was proven to be the key gene involved in this process by single cell sequencing analysis, CCK-8 assay and a clonogenic survival assay. In high-DRS patients, the cancer-immunity cycle is attenuated because the antitumor cytotoxicity of CD8+ T cells is inhibited by immune checkpoints. Preclinically, the overexpression of EFEMP2 induced radioresistance and enhancing the efficacy of programmed cell death ligand-1 (PD-L1) blockade in GL261-bearing mice. The combination of irradiation and anti-PD-L1 therapy had a synergistic effect on GBM murine models in which EFEMP2 was overexpressed.

Conclusion: Our study bioinformatically and experimentally reveals the molecular landscape of disulfidptosis in GBM, develops a predictive signature for predicting prognosis as well as radioresistance, and provides a synergistic treatment that combines radiotherapy with immunotherapy for radioresistant GBM patients with high DRS or EFEMP2 expression.

背景:程序性细胞死亡(PCD)调制的放射耐药是胶质母细胞瘤(GBM)治疗失败的主要原因之一。二硫下垂是一种新发现的PCD形式,在GBM的进展中起着至关重要的作用。然而,在GBM中,双重下垂、放射敏感性和放疗(RT)之间的关系尚不清楚。方法:系统分析1075例GBM患者的二硫中毒相关基因,构建二硫中毒相关基因标记(DRS)。充分探讨了DRS与患者预后及免疫微环境的相关性。通过单细胞测序分析研究DRS和EFEMP2对放疗疗效的影响,并通过体外和体内实验验证。结果:通过多队列多变量Cox回归分析、受试者工作特征(ROC)曲线分析和决策曲线分析(DCA), DRS被确定为GBM可靠、独立的预后生物标志物。高DRS以辐射耐药为特征,单细胞测序分析、CCK-8实验和克隆生存实验证明EFEMP2是参与这一过程的关键基因。在高drs患者中,由于CD8+ T细胞的抗肿瘤细胞毒性被免疫检查点抑制,癌症免疫周期被减弱。临床前,EFEMP2的过表达诱导gl261小鼠的放射耐药,并增强程序性细胞死亡配体-1 (PD-L1)阻断的效果。照射联合抗pd - l1治疗对EFEMP2过表达的GBM小鼠模型具有协同作用。结论:我们的研究通过生物信息学和实验揭示了GBM中二亢的分子景观,为预测预后和放射耐药提供了预测特征,并为高DRS或EFEMP2表达的放射耐药GBM患者提供了放射治疗与免疫治疗相结合的协同治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
2.80%
发文量
577
审稿时长
2 months
期刊介绍: The "Journal of Cancer Research and Clinical Oncology" publishes significant and up-to-date articles within the fields of experimental and clinical oncology. The journal, which is chiefly devoted to Original papers, also includes Reviews as well as Editorials and Guest editorials on current, controversial topics. The section Letters to the editors provides a forum for a rapid exchange of comments and information concerning previously published papers and topics of current interest. Meeting reports provide current information on the latest results presented at important congresses. The following fields are covered: carcinogenesis - etiology, mechanisms; molecular biology; recent developments in tumor therapy; general diagnosis; laboratory diagnosis; diagnostic and experimental pathology; oncologic surgery; and epidemiology.
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