脑胶质母细胞瘤附近的祖细胞/干细胞标志物:GD3神经节苷脂和NG2蛋白聚糖的表达

G. Lama, A. Mangiola, G. Proietti, A. Colabianchi, C. Angelucci, A. D'Alessio, P. De Bonis, M. Geloso, L. Lauriola, Elena Binda, F. Biamonte, M. G. Giuffrida, A. Vescovi, G. Sica
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引用次数: 31

摘要

胶质母细胞瘤(GBM)周围组织的特征是转化研究的焦点,因为肿瘤复发总是发生在这个区域。我们研究了祖细胞/干细胞标志物GD3神经节苷脂和NG2蛋白多糖在GBM、瘤周组织(瘤旁脑,BAT)和从GBM (GCSCs)和BAT (PCSCs)分离的癌症干细胞样细胞(CSCs)中的表达。对40例GBM和BAT配对标本进行GD3和NG2免疫组化。采用双免疫荧光法对血管壁ng2阳性细胞进行表征。研究GD3和NG2在GCSCs和PCSCs中的表达,并在Scid/bg小鼠中评估其致瘤性。GD3和NG2在肿瘤组织中的表达高于BAT。与肿瘤细胞有无无关,NG2随肿瘤边缘距离的增加而降低,而GD3与肿瘤浸润相关。在BAT中,NG2在周细胞中与&agr;-平滑肌肌动蛋白(&agr;-SMA)共表达,在内皮细胞中与巢蛋白共表达。NG2 mRNA和蛋白在gcsc中表达水平较高,而GD3合成酶在2个CSC群体中表达水平相似。PCSCs的致瘤性低于GCSCs。这些数据表明,GD3和NG2可能参与了GBM周围组织复杂微环境中发生的致瘤前/致瘤前事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progenitor/Stem Cell Markers in Brain Adjacent to Glioblastoma: GD3 Ganglioside and NG2 Proteoglycan Expression
Characterization of tissue surrounding glioblastoma (GBM) is a focus for translational research because tumor recurrence invariably occurs in this area. We investigated the expression of the progenitor/stem cell markers GD3 ganglioside and NG2 proteoglycan in GBM, peritumor tissue (brain adjacent to tumor, BAT) and cancer stem-like cells (CSCs) isolated from GBM (GCSCs) and BAT (PCSCs). GD3 and NG2 immunohistochemistry was performed in paired GBM and BAT specimens from 40 patients. Double-immunofluorescence was carried out to characterize NG2-positive cells of vessel walls. GD3 and NG2 expression was investigated in GCSCs and PCSCs whose tumorigenicity was also evaluated in Scid/bg mice. GD3 and NG2 expression was higher in tumor tissue than in BAT. NG2 decreased as the distance from tumor margin increased, regardless of the tumor cell presence, whereas GD3 correlated with neoplastic infiltration. In BAT, NG2 was coexpressed with &agr;-smooth muscle actin (&agr;-SMA) in pericytes and with nestin in the endothelium. Higher levels of NG2 mRNA and protein were found in GCSCs while GD3 synthase was expressed at similar levels in the 2 CSC populations. PCSCs had lower tumorigenicity than GCSCs. These data suggest the possible involvement of GD3 and NG2 in pre/pro-tumorigenic events occurring in the complex microenvironment of the tissue surrounding GBM.
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