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A new alternative mechanism in glioblastoma vascularization: tubular vasculogenic mimicry
Author(s) -
Soufiane El Hallani,
Blandine Boisselier,
Florent Péglion,
Audrey Rousseau,
Carole Colin,
Ahmed Idbaïh,
Y. Marie,
Karima Mokhtari,
JeanLéon Thomas,
Anne Eichmann,
J. Y. Delattre,
Andrew J. Maniotis,
Marc Sanson
Publication year - 2010
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awq044
Subject(s) - vasculogenic mimicry , vasculogenesis , glioblastoma , stem cell , mural cell , cancer research , pathology , biology , endothelial stem cell , endothelium , blood–brain barrier , ve cadherin , in vitro , microbiology and biotechnology , progenitor cell , medicine , neuroscience , central nervous system , cancer , biochemistry , genetics , endocrinology , metastasis
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.

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