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外泌体作为胶质母细胞瘤新治疗策略的潜力。

The potential of exosomes as a new therapeutic strategy for glioblastoma.

机构信息

Faculty of Pharmacy, FFUC, University of Coimbra, Coimbra 3000-548, Portugal.

Faculty of Pharmacy, FFUC, University of Coimbra, Coimbra 3000-548, Portugal; Coimbra Chemistry Centre, Institute of Molecular Sciences - IMS, Department of Chemistry, University of Coimbra, Coimbra 3004 535, Portugal.

出版信息

Eur J Pharm Biopharm. 2024 Oct;203:114460. doi: 10.1016/j.ejpb.2024.114460. Epub 2024 Aug 31.

DOI:10.1016/j.ejpb.2024.114460
PMID:39218361
Abstract

Glioblastoma (GBM) stands for the most common and aggressive type of brain tumour in adults. It is highly invasive, which explains its short rate of survival. Little is known about its risk factors, and current therapy is still ineffective. Hence, efforts are underway to develop novel and effective treatment approaches against this type of cancer. Exosomes are being explored as a promising strategy for conveying and delivering therapeutic cargo to GBM cells. They can fuse with the GBM cell membrane and, consequently, serve as delivery systems in this context. Due to their nanoscale size, exosomes can cross the blood-brain barrier (BBB), which constitutes a significant hurdle to most chemotherapeutic drugs used against GBM. They can subsequently inhibit oncogenes, activate tumour suppressor genes, induce immune responses, and control cell growth. However, despite representing a promising tool for the treatment of GBM, further research and clinical studies regarding exosome biology, engineering, and clinical applications still need to be completed. Here, we sought to review the application of exosomes in the treatment of GBM through an in-depth analysis of the scientific and clinical studies on the entire process, from the isolation and purification of exosomes to their design and transformation into anti-oncogenic drug delivery systems. Surface modification of exosomes to enhance BBB penetration and GBM-cell targeting is also a topic of discussion.

摘要

胶质母细胞瘤(GBM)是成人中最常见和侵袭性最强的脑肿瘤类型。它具有很强的侵袭性,这解释了它存活率低的原因。目前对于其危险因素知之甚少,且现行的治疗方法仍然效果不佳。因此,人们正在努力开发针对这种癌症的新型有效治疗方法。外泌体作为一种有前途的策略,正在被探索用于向 GBM 细胞传递和输送治疗性货物。它们可以与 GBM 细胞膜融合,因此在这种情况下可以作为递送系统。由于其纳米级尺寸,外泌体可以穿过血脑屏障(BBB),这是大多数用于治疗 GBM 的化疗药物面临的重大障碍。它们可以随后抑制癌基因,激活肿瘤抑制基因,诱导免疫反应,并控制细胞生长。然而,尽管外泌体代表了治疗 GBM 的一种有前途的工具,但关于外泌体生物学、工程和临床应用的进一步研究和临床研究仍有待完成。在这里,我们通过深入分析从外泌体的分离和纯化到设计和转化为抗致癌药物递送系统的整个过程的科学和临床研究,旨在探讨外泌体在治疗 GBM 中的应用。还讨论了对外泌体进行表面修饰以增强 BBB 穿透和 GBM 细胞靶向的问题。

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