1Department of Biochemistry and Biomedicine, School of Life Sciences, University of Sussex, Brighton, BN1 9QG UK.
2Pharmacy and Biomolecular Sciences, University of Brighton, Brighton, BN2 4GJ UK.
Commun Biol. 2019 Aug 19;2:315. doi: 10.1038/s42003-019-0560-x. eCollection 2019.
Glioblastoma (GBM) is one of the most aggressive solid tumors for which treatment options and biomarkers are limited. Small extracellular vesicles (sEVs) produced by both GBM and stromal cells are central in the inter-cellular communication that is taking place in the tumor bulk. As tumor sEVs are accessible in biofluids, recent reports have suggested that sEVs contain valuable biomarkers for GBM patient diagnosis and follow-up. The aim of the current study was to describe the protein content of sEVs produced by different GBM cell lines and patient-derived stem cells. Our results reveal that the content of the sEVs mirrors the phenotypic signature of the respective GBM cells, leading to the description of potential informative sEV-associated biomarkers for GBM subtyping, such as CD44. Overall, these data could assist future GBM in vitro studies and provide insights for the development of new diagnostic and therapeutic methods as well as personalized treatment strategies.
胶质母细胞瘤(GBM)是最具侵袭性的实体肿瘤之一,其治疗选择和生物标志物有限。GBM 和基质细胞产生的小细胞外囊泡(sEVs)是发生在肿瘤块中的细胞间通讯的核心。由于肿瘤 sEVs 可在生物流体中获得,最近的报道表明 sEVs 包含用于 GBM 患者诊断和随访的有价值的生物标志物。本研究的目的是描述不同 GBM 细胞系和患者来源的干细胞产生的 sEV 的蛋白质含量。我们的结果表明,sEV 的含量反映了相应 GBM 细胞的表型特征,从而描述了用于 GBM 亚型分类的潜在信息丰富的 sEV 相关生物标志物,例如 CD44。总的来说,这些数据可以帮助未来进行 GBM 的体外研究,并为开发新的诊断和治疗方法以及个性化治疗策略提供见解。