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腱生蛋白-C在胶质母细胞瘤中的分布模式:与血管生成及肿瘤细胞增殖的相关性

Distribution pattern of tenascin-C in glioblastoma: correlation with angiogenesis and tumor cell proliferation.

作者信息

Behrem Senija, Zarković Kamelija, Eskinja Neven, Jonjić Nives

机构信息

Department of Pathology, Medical Faculty, University of Rijeka, Rijeka, Croatia.

出版信息

Pathol Oncol Res. 2005;11(4):229-35. doi: 10.1007/BF02893856. Epub 2005 Dec 31.

Abstract

Tenascin-C (TN-C) is an extracellular matrix protein which participates in different processes like normal fetal development, wound healing, inflammation, keloids and rheumatoid arthritis. Furthermore, the immunostaining for TN-C is seen in the stroma of various malignant tumors as in glioblastoma multiforme (GBM), however, the significance of these findings is still not clear. In this study 62 GBM samples were analyzed immunohistochemically for distribution patterns of TN-C and correlated with angiogenesis and tumor cell proliferation. Tenascin-C in GBM localizes in two compartments, perivascular and intercellular space. Intercellular tenascin-C (TN-C ic) showed focal distribution in 66%, and diffuse one in 34% of cases. Perivascular tenascin-C (TN-C pv) showed strong correlation with microvascular density (MVD) and vascular endothelial growth factor (VEGF) expression. Moreover, it seems that TN-C pv enhanced the effect of VEGF. Intercellular TN-C did not correlate with MVD and VEGF expression, but showed strong correlation with proliferation index. Furthermore, tumors with diffuse TN-C ic expression had higher proliferation indices than tumors with focal TN-C expression. Our results indicate that TN-C plays a role in angiogenesis and tumor cell proliferation, but beside the intensity of expression, the distribution patterns are also important in these processes. This study also suggests that perivascular and intercellular TN-C compartments have probably different sources and different roles in GBM.

摘要

腱生蛋白-C(TN-C)是一种细胞外基质蛋白,参与多种生理过程,如正常胎儿发育、伤口愈合、炎症、瘢痕疙瘩和类风湿性关节炎。此外,在多形性胶质母细胞瘤(GBM)等各种恶性肿瘤的基质中可观察到TN-C的免疫染色,然而,这些发现的意义仍不明确。在本研究中,对62例GBM样本进行免疫组织化学分析,以检测TN-C的分布模式,并与血管生成和肿瘤细胞增殖进行相关性分析。GBM中的腱生蛋白-C定位于两个区域,即血管周围和细胞间隙。细胞间腱生蛋白-C(TN-C ic)在66%的病例中呈局灶性分布,34%的病例呈弥漫性分布。血管周围腱生蛋白-C(TN-C pv)与微血管密度(MVD)和血管内皮生长因子(VEGF)表达呈强相关性。此外,TN-C pv似乎增强了VEGF的作用。细胞间TN-C与MVD和VEGF表达无相关性,但与增殖指数呈强相关性。此外,弥漫性TN-C ic表达的肿瘤比局灶性TN-C表达的肿瘤具有更高的增殖指数。我们的结果表明,TN-C在血管生成和肿瘤细胞增殖中起作用,但除了表达强度外,分布模式在这些过程中也很重要。本研究还表明,血管周围和细胞间TN-C区域在GBM中可能具有不同的来源和不同的作用。

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