UMR975, Hôpital de la Salpêtrière, Université Pierre et Marie Curie, Paris, France.
Brain. 2010 Apr;133(Pt 4):973-82. doi: 10.1093/brain/awq044.
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.
胶质母细胞瘤是最血管生成的人类肿瘤之一,内皮细胞增殖是该疾病的标志。为了优化抗血管生成治疗,需要更好地了解胶质母细胞瘤的血管生成,该治疗已显示出高但短暂的疗效。我们分析了人类胶质母细胞瘤组织,发现了由肿瘤细胞形成的非内皮细胞衬里的血管(管状型的血管生成模拟)。我们假设具有干细胞特性的 CD133+胶质母细胞瘤细胞可能表达促血管分子,使它们能够从头形成血管。我们在体外证明了神经胶质瘤干细胞样细胞能够进行血管生成和内皮细胞相关基因的表达。此外,这些神经胶质瘤干细胞样细胞的一部分可以转分化为血管平滑肌样细胞。我们在这里描述了一种新的胶质母细胞瘤血管生成替代机制,并为抗血管治疗策略开辟了新的视角。