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:Mesenchymal stem cell-based delivery systems for the treatment of brain tumors.
脑肿瘤属于最致命的癌症类型之列,在儿童和成人人群中均导致高死亡率。
脑肿瘤是致死率最高的癌症类型之一,在儿童和成人中均造成较高死亡率。其固有的侵袭性生物学特征、复杂的周围微环境以及现有标准治疗方式疗效相对有限,使治疗面临重大障碍。间充质干细胞(MSC)具有选择性迁移至肿瘤部位的能力,也可作为多种治疗药物的递送载体,因此受到肿瘤研究领域广泛关注。本综述介绍 MSC 及其衍生物(如外泌体和工程化载体)在脑肿瘤治疗中的多种潜在作用,涵盖 MSC 递送化疗药物、溶瘤病毒和治疗性基因,基于外泌体的干预,利用纳米技术提高靶向精度,以及通过工程化 MSC 来源细胞因子调节肿瘤行为等策略。尽管前景可期,MSC 可能促进肿瘤生长以及需要精准递送系统等问题仍令人担忧。本文强调,需开展更多研究以改进 MSC 相关策略,尤其要合理工程化改造 MSC 及其衍生物,用于多模式治疗,从而提高恶性脑肿瘤治疗的特异性、疗效和安全性。
Brain tumors rank among the most lethal cancer types, accounting for high mortality rates in both pediatric and adult populations. They present formidable therapeutic obstacles owing to their intrinsically aggressive biology, the complexity of their surrounding microenvironment, and the relatively poor efficacy of existing standard treatment modalities. Mesenchymal stem cells (MSCs) have garnered significant interest in oncology research due to their inherent ability to migrate selectively toward tumor sites and their versatility as delivery vehicles for a wide range of therapeutic agents. This review highlights the diverse therapeutic roles of MSCs and their derivatives, such as exosomes and engineered vectors, in brain tumor management. It encompasses key therapeutic strategies leveraging MSCs, including MSC-mediated delivery of chemotherapeutic agents, oncolytic viruses, and therapeutic genes; exosome-based interventions; nanotechnology-enhanced targeting precision; and the modulation of tumor behavior by engineered MSC-derived cytokines. Despite their promise, concerns remain regarding the potential for MSCs to promote tumor growth and the need for precise delivery systems. This review highlights the crucial need for additional research to refine MSC-based strategies, particularly through the rational engineering of MSCs and their derivatives for multimodal therapeutic applications, with the goal of enhancing specificity, efficacy, and safety in the treatment of malignant brain tumors.
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