A new alternative mechanism in glioblastoma vascularization: tubular vasculogenic mimicry

被引:282
作者
El Hallani, Soufiane [1 ]
Boisselier, Blandine [1 ]
Peglion, Florent [1 ]
Rousseau, Audrey [2 ]
Colin, Carole [3 ]
Idbaih, Ahmed [1 ,4 ]
Marie, Yannick [1 ]
Mokhtari, Karima [2 ]
Thomas, Jean-Leon [1 ]
Eichmann, Anne [5 ]
Delattre, Jean-Yves [1 ,4 ]
Maniotis, Andrew J. [6 ]
Sanson, Marc [1 ,4 ]
机构
[1] Univ Paris 06, Hop La Pitie Salpetriere, UMR975, F-75013 Paris, France
[2] Hop La Pitie Salpetriere, Serv Neuropathol Raymond Escourolle, F-75013 Paris, France
[3] Univ Mediterranee, Fac Med Timone, CRO2, UMR911, F-13000 Marseille, France
[4] Hop La Pitie Salpetriere, Serv Neurol Mazarin, F-75013 Paris, France
[5] Coll France, INSERM, U833, F-75005 Paris, France
[6] Univ Illinois, Dept Pathol, Chicago, IL 60612 USA
关键词
glioblastoma; angiogenesis; vasculogenic mimicry; stem cell; PHASE-II TRIAL; BLOOD-VESSELS; IN-VITRO; MESENCHYMAL DIFFERENTIATION; EMBRYONIC VASCULOGENESIS; ENDOTHELIAL-CELLS; TUMOR VESSELS; STEM-CELLS; ANGIOGENESIS; PROLIFERATION;
D O I
10.1093/brain/awq044
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
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.
引用
收藏
页码:973 / 982
页数:10
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