CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
我们的工作确立了CD81作为连接放射抵抗与免疫逃逸的关键桥梁,其通过维持GBM中CD274的丰度发挥作用,并突显CD81作为优化放射免疫治疗的有前景的治疗靶点。
英文原题:Review of biomarkers for response to immunotherapy in HNSCC microenvironment.
头颈部鳞状细胞癌是全球最常见的癌症类型之一。
头颈部鳞状细胞癌是全球最常见的癌症类型之一。尽管手术、放疗、化疗和靶向治疗等多种治疗方法已广泛应用于HNSCC的诊断和治疗,但过去几十年中患者的生存预后并未显著改善。作为一种新兴的治疗方法,免疫治疗在R/M HNSCC中显示出令人振奋的治疗效果。然而,目前的筛选方法仍不充分,迫切需要可靠的预测性生物标志物用于个性化临床管理和新的治疗策略。本综述总结了免疫治疗在HNSCC中的应用,全面分析了现有的关于HNSCC免疫治疗的生物信息学研究,评估了当前肿瘤免疫异质性和免疫治疗的方法,旨在筛选具有潜在预测意义的分子标志物。其中,PD-1作为现有免疫药物的靶点具有明显的预测相关性。克隆性TMB是HNSCC免疫治疗的潜在生物标志物。其他分子,包括IFN-γ、CXCL、CTLA-4、MTAP、SFR4/CPXM1/COL5A1、TILs、CAFs、外泌体和外周血指标,可能对肿瘤免疫微环境和免疫治疗预后具有提示意义。
Head and neck squamous cell carcinoma are one of the most common types of cancer worldwide. Although a variety of treatment methods such as surgery, radiotherapy, chemotherapy, and targeted therapy are widely used in diagnosing and treating HNSCC, the survival prognosis of patients has not been significantly improved in the past decades. As an emerging treatment approach, immunotherapy has shown exciting therapeutic effects in R/M HNSCC. However, the current screening methods are still insufficient, and there is a significant need for reliable predictive biomarkers for personalized clinical management and new therapeutic strategies. This review summarized the application of immunotherapy in HNSCC, comprehensively analyzed the existing bioinformatic studies on immunotherapy in HNSCC, evaluated the current methods of tumor immune heterogeneity and immunotherapy, and aimed to screen molecular markers with potential predictive significance. Among them, PD-1 has obvious predictive relevance as the target of existing immune drugs. Clonal TMB is a potential biomarker for HNSCC immunotherapy. The other molecules, including IFN-γ, CXCL, CTLA-4, MTAP, SFR4/CPXM1/COL5A1, TILs, CAFs, exosomes, and peripheral blood indicators, may have suggestive significance for tumor immune microenvironment and prognosis of immunotherapy.
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