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评估胶质母细胞瘤瘤周组织中 CD105 和巢蛋白的表达与血管生成的关系。

Assessment of angiogenesis by CD105 and nestin expression in peritumor tissue of glioblastoma.

机构信息

Institute of Histology and Embryology, Faculty of Medicine, Catholic University of the Sacred Heart, Largo Francesco Vito 1, I-00168 Rome, Italy.

出版信息

Int J Oncol. 2011 Jan;38(1):41-9.

Abstract

Angiogenesis in the peritumor tissue of glioblastoma (GBM) is still an open field of research. This study investigates neovascularization in the tumor surrounding areas by examining CD105 and nestin expression along with microvessel density (MVD) with the aim of establishing their possible prognostic significance. Angiogenesis was also confirmed by investigating, in vessel walls, the presence of pericytes, which are multipotent stem cells, expressing α-smooth muscle actin (α-SMA). In our study, including 40 GBM patients, tissue samples were obtained from tumors (first area) and white matter at a distance <1 cm (second area) and between 1 and 3.5 cm (third area) from the tumor margin. CD105 and nestin were detected by immunohistochemistry in hyperplastic endothelium of GBM and peritumor tissue, and occasionally coexpressed or colocalized. Pericytes encircling hyperplastic endothelium were evident in all three areas. Univariate analysis revealed that patients with a CD105-MVD value ≥8 in the third area have a significantly shorter survival time and Cox analysis indicated an about 3.5-fold increase in death risk in the same patients. These results demonstrate that a tumor neoangiogenesis occurs in GBM peritumor tissue with intimate involvement of pericytes. CD105-MVD in the area located at a greater distance from the tumor margin carries prognostic significance.

摘要

成胶质细胞瘤(GBM)肿瘤周围组织的血管生成仍然是一个研究领域。本研究通过检测 CD105 和巢蛋白的表达以及微血管密度(MVD)来研究肿瘤周围区域的新生血管形成,并旨在确定其可能的预后意义。还通过研究血管壁中是否存在多能干细胞周细胞来确认血管生成,周细胞表达α-平滑肌肌动蛋白(α-SMA)。在我们的研究中,包括 40 名 GBM 患者,组织样本取自肿瘤(第一区)和距离肿瘤边缘<1cm(第二区)和 1 到 3.5cm(第三区)的白质。CD105 和巢蛋白通过免疫组化在 GBM 和肿瘤周围组织的增生内皮细胞中被检测到,并且偶尔共表达或共定位。在所有三个区域都可以明显看到围绕增生内皮细胞的周细胞。单因素分析显示,第三区 CD105-MVD 值≥8 的患者生存时间明显缩短,Cox 分析表明,同一患者的死亡风险增加约 3.5 倍。这些结果表明,GBM 肿瘤周围组织中存在肿瘤新生血管生成,周细胞密切参与其中。距离肿瘤边缘较远区域的 CD105-MVD 具有预后意义。

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