| Literature DB >> 20375132 |
Soufiane El Hallani1, Blandine Boisselier, Florent Peglion, Audrey Rousseau, Carole Colin, Ahmed Idbaih, Yannick Marie, Karima Mokhtari, Jean-Léon Thomas, Anne Eichmann, Jean-Yves Delattre, Andrew J Maniotis, Marc Sanson.
Abstract
Glioblastoma is one of the most angiogenic human tumours and endothelial proliferation is a hallmark of the disease. A better understanding of glioblastoma vasculature is needed to optimize anti-angiogenic therapy that has shown a high but transient efficacy. We analysed human glioblastoma tissues and found non-endothelial cell-lined blood vessels that were formed by tumour cells (vasculogenic mimicry of the tubular type). We hypothesized that CD133+ glioblastoma cells presenting stem-cell properties may express pro-vascular molecules allowing them to form blood vessels de novo. We demonstrated in vitro that glioblastoma stem-like cells were capable of vasculogenesis and endothelium-associated genes expression. Moreover, a fraction of these glioblastoma stem-like cells could transdifferentiate into vascular smooth muscle-like cells. We describe here a new mechanism of alternative glioblastoma vascularization and open a new perspective for the antivascular treatment strategy.Entities:
Mesh:
Year: 2010 PMID: 20375132 PMCID: PMC4861203 DOI: 10.1093/brain/awq044
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501