Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Department of Comparative Biomedicine and Food Science, University of Padua, Padua, Italy; Departments of Neurology and Radiology, Massachusetts General Hospital, Boston, MA 02114, USA; Neuroscience Program, Harvard Medical School, Boston, MA 02115, USA.
Cell Rep. 2020 Feb 18;30(7):2065-2074.e4. doi: 10.1016/j.celrep.2020.01.073.
Glioblastoma (GBM) is characterized by aberrant vascularization and a complex tumor microenvironment. The failure of anti-angiogenic therapies suggests pathways of GBM neovascularization, possibly attributable to glioblastoma stem cells (GSCs) and their interplay with the tumor microenvironment. It has been established that GSC-derived extracellular vesicles (GSC-EVs) and their cargoes are proangiogenic in vitro. To further elucidate EV-mediated mechanisms of neovascularization in vitro, we perform RNA-seq and DNA methylation profiling of human brain endothelial cells exposed to GSC-EVs. To correlate these results to tumors in vivo, we perform histoepigenetic analysis of GBM molecular profiles in the TCGA collection. Remarkably, GSC-EVs and normal vascular growth factors stimulate highly distinct gene regulatory responses that converge on angiogenesis. The response to GSC-EVs shows a footprint of post-transcriptional gene silencing by EV-derived miRNAs. Our results provide insights into targetable angiogenesis pathways in GBM and miRNA candidates for liquid biopsy biomarkers.
胶质母细胞瘤(GBM)的特征是血管生成异常和肿瘤微环境复杂。抗血管生成疗法的失败表明 GBM 新生血管的途径可能归因于胶质母细胞瘤干细胞(GSCs)及其与肿瘤微环境的相互作用。已经证实 GSC 来源的细胞外囊泡(GSC-EVs)及其货物在体外具有促血管生成作用。为了进一步阐明 EV 介导的体外新生血管化的机制,我们对暴露于 GSC-EVs 的人脑血管内皮细胞进行了 RNA-seq 和 DNA 甲基化分析。为了将这些结果与体内肿瘤相关联,我们对 TCGA 集合中的 GBM 分子谱进行了组织表观遗传分析。值得注意的是,GSC-EVs 和正常血管生长因子刺激高度不同的基因调控反应,这些反应集中在血管生成上。对 GSC-EVs 的反应显示出 EV 衍生的 miRNA 进行转录后基因沉默的特征。我们的结果为 GBM 中可靶向的血管生成途径和液体活检生物标志物的 miRNA 候选物提供了深入了解。