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:Engineered Macrophage Exosomes Deliver Drug-Targeted Therapy for Breast Cancer.
Engineered Macrophage Exosomes Deliver Drug-Targeted Therapy for Breast Cancer.
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乳腺癌是一种高度普遍的恶性肿瘤,具有高复发率和高死亡率的特点;它主要发生在肿瘤细胞扩散到身体外周区域时。巨噬细胞对乳腺癌的增殖和转移有显著影响。这些细胞产生的外泌体在抑制癌细胞扩散方面表现出广泛的能力。它们对乳腺癌细胞具有非常特异的靶向特性,并通过改变肿瘤内的免疫环境来抑制癌细胞的增殖。本研究探讨了开发巨噬细胞来源外泌体的方法,例如使用蛋白偶联的外泌体膜来保护递送内容物、创建多功能仿生颗粒以及利用超声融合来保护递送内容物。此外,本文还讨论了利用有机和无机材料生产巨噬细胞外泌体的最新进展。总体而言,构建由巨噬细胞外泌体介导的药物递送系统可能极大地有益于乳腺癌的靶向治疗。
Breast cancer is a highly widespread form of malignant tumor characterized by a high rate of recurrence and mortality; it primarily occurs when tumor cells spread to peripheral regions of the body. Macrophages have a significant impact on the proliferation and metastasis of breast cancer.
The exosomes generated by these cells exhibit an extensive spectrum of capabilities in suppressing the spread of cancer cells. These feature very specific targeting properties for breast cancer cells and inhibit the proliferation of cancer cells by altering the immune milieu within the tumor.
This study investigates methods for developing macrophage-derived exosomes, such as using protein-coupled exosome membranes to protect delivery contents, creating multifunctional biomimetic particles, and utilizing ultrasonic fusion to protect delivery contents.
Furthermore, this paper addresses recent advances in producing macrophage exosomes from organic and inorganic materials. In general, targeted treatment for breast cancer could benefit greatly from creating drug delivery systems mediated by macrophage exosomes.
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