| Literature DB >> 32075753 |
Rocco Lucero1, Valentina Zappulli2, Alessandro Sammarco3, Oscar D Murillo1, Pike See Cheah4, Srimeenakshi Srinivasan5, Eric Tai6, David T Ting6, Zhiyun Wei7, Matthew E Roth1, Louise C Laurent5, Anna M Krichevsky7, Xandra O Breakefield8, Aleksandar Milosavljevic9.
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.Entities:
Keywords: angiogenesis; biomarker; cancer stem cell; deconvolution; exRNA; extracellular vesicle; glioblastoma; miRNA; reprogramming; tumor microenvironment
Year: 2020 PMID: 32075753 PMCID: PMC7148092 DOI: 10.1016/j.celrep.2020.01.073
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423