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Angiogenesis in craniopharyngiomas: Microvascular density and tissue expression of the vascular endothelial growth factor (VEGF) and endostatin

机译:颅咽炎的血管生成:微血管密度和血管内皮生长因子(VEGF)和内皮抑素的组织表达

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摘要

Craniopharyngiomas are benign tumors of the sellar region generally associated with endocrine abnormality and often locally aggressive. Several studies have demonstrated that angiogenesis or neovascularization plays an important role in tumoral growth. The microvascular density (MVD) of craniopharyngiomas was determined in tumor tissue samples from a reference neurosurgery center located in southern Brazil using immunohistochemical methods for two endothelial markers, CD34 and CD105 (endoglin). In addition, tissue expression was determined for an angiogenesis stimulatory factor and for one of its inhibitors, the vascular endothelial growth factor (VEGF) and endostatin, respectively. Endothelial cell immunoreactivity for CD34 and CD105 was observed scattered within the stroma. MVD determined using CD105 antigen was significantly lower than the results obtained by using CD34 antigen. There was no association between the two endothelial markers and tumor extension. The epithelial component showed different degrees of immunoreactivity for VEGF and endostatin in all samples analyzed. We were not able to establish a relationship between angiogenesis in craniopharyngiomas and tumor extension with the endothelial markers used in this study. The investigated vascularization stimulatory and inhibitory factors showed no relation with MVD. We believe that CD105 antigen can be a more specific endothelial marker for tumor angiogenesis than CD34 antigen.
机译:颅咽管瘤是蝶鞍区的良性肿瘤,通常与内分泌异常有关,通常局部侵袭性。多项研究表明,血管生成或新血管形成在肿瘤生长中起重要作用。使用免疫组织化学方法针对两种内皮标记物CD34和CD105(endoglin),从巴西南部参考神经外科中心的肿瘤组织样本中确定了颅咽神经瘤的微血管密度(MVD)。此外,分别确定了血管生成刺激因子及其抑制剂之一血管内皮生长因子(VEGF)和内皮抑素的组织表达。观察到CD34和CD105的内皮细胞免疫反应性分散在基质内。使用CD105抗原测定的MVD明显低于使用CD34抗原获得的结果。两种内皮标记物与肿瘤扩展之间没有关联。在所有分析的样品中,上皮成分对VEGF和内皮抑素的免疫反应程度不同。我们无法使用本研究中使用的内皮标记物建立颅咽管瘤血管生成与肿瘤扩展之间的关系。研究的血管生成刺激和抑制因素与MVD无关。我们相信,CD105抗原可以是比CD34抗原更特异性的肿瘤血管生成内皮标记。

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