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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Revolutionizing cancer treatment: engineering mesenchymal stem cell-derived small extracellular vesicles.
Revolutionizing cancer treatment: engineering mesenchymal stem cell-derived small extracellular vesicles.
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近年来,使用外泌体是治疗癌症的重要方法之一。间充质干细胞是多能干细胞,是调节免疫系统并且重要的是抑制针对肿瘤细胞的免疫反应的非常被看好的来源。从间充质干细胞中提取的小细胞外囊泡(small EVs)可以通过调节信号通路,具有将靶向药物递送至癌细胞以及肿瘤的治疗方法。在癌症治疗中使用外泌体存在需要改进的挑战。对 small EVs 进行工程化改造可以恢复外泌体的作用,例如药物递送和治疗工具。在来源于 small EVs 的间充质干细胞领域,有临床前和临床研究证明这些方法在癌症领域中的疗效。考虑到大规模生产等问题,工程化 small EVs 作为癌症治疗方法,结果表明它们保留了其所来源细胞的大部分特征,这些特征负责其驱动肿瘤微环境中积极变化的免疫调节影响。
In recent years, use of exosomes is one of the important approaches to treat cancer. Mesenchymal stem cells are multipotent stem cells which are very putative sources for modulating the immune system and importantly inhibiting immune responses against tumor cells. Small extracellular vesicles (small EVs) are extracted from mesenchymal stem cells can have therapeutic approaches for delivering targeted drugs to cancer cells and also tumors via regulation of signaling pathways. There are challenges in use of exosomes in cancer treatment which need to be improved.
Engineering in small EVs can recover the role of exosomes such as drug delivery and therapeutic tools. There are preclinical and clinical studies in the field of mesenchymal stem cells derived from small EVs which demonstrates efficacy of these approaches in the field of cancer.
In consideration of problems in large scale production and so on, engineered small EVs as treatment approaches for cancers, it is resulted that they retain most characteristics of cells which are derived from, are responsible for their immunomodulatory impacts driving positive changes in the tumor microenvironment.
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