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Endosialin (CD248) is a marker of tumor-associated pericytes in high-grade glioma

机译:Endosialin(CD248)是高级神经胶质瘤中肿瘤相关周细胞的标志物

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Gliomas are the most frequent primary tumors of the central nervous system in adults. The most prevalent and aggressive subclass of these is glioblastoma multiforme, which is characterized by massive neovascularization. Endosialin (CD248) has generated interest as a target for antiangiogenic therapy following reports that its expression is upregulated on angiogenic endothelial cells. We demonstrate here that endosialin is not expressed in normal human adult brain but is strongly upregulated in the angiogenic vasculature of all high-grade glioma specimens examined. However, by taking advantage of a technique which allows for multiple fluorescent labeling of formalin-fixed paraffin-embedded archival sections, we demonstrate unambiguously that endosialin is not expressed by the glioma endothelial cells but on closely associated perivascular cells. With increasing awareness that targeting pericytes is an attractive adjunct in antiangiogenic therapy, this finding has important implications for understanding the molecular mechanisms regulating angiogenesis in these highly vascularized tumors.
机译:神经胶质瘤是成年人中最常见的中枢神经系统原发肿瘤。其中最普遍和最具侵略性的亚类是多形性胶质母细胞瘤,其特征是大量新生血管形成。有报道称内皮素(CD248)在血管生成内皮细胞中表达上调,因此其作为抗血管生成治疗的靶标引起了人们的兴趣。我们在这里证明内皮唾液酸蛋白在正常人的成年大脑中不表达,但是在所有检查的所有高级神经胶质瘤标本的血管生成脉管系统中强烈上调。但是,通过利用允许对福尔马林固定石蜡包埋的档案切片进行多次荧光标记的技术,我们可以明确证明内皮唾液酸蛋白不是由神经胶质瘤内皮细胞表达的,而是在紧密相关的血管周细胞上表达的。随着人们越来越认识到靶向周细胞是抗血管生成治疗中的一种有吸引力的辅助手段,这一发现对于理解调节这些高度血管化肿瘤中血管生成的分子机制具有重要意义。

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