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脑胶质瘤来源的含有 miRNA 的细胞外囊泡通过重编程脑内皮细胞诱导血管生成。

Glioma-Derived miRNA-Containing Extracellular Vesicles Induce Angiogenesis by Reprogramming Brain Endothelial Cells.

机构信息

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.

出版信息

Cell Rep. 2020 Feb 18;30(7):2065-2074.e4. doi: 10.1016/j.celrep.2020.01.073.

Abstract

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.

摘要

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。

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