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Is the Wnt/β catenin signalling pathway activated in Seminoma?: An immunohistochemical study

机译:精原细胞瘤中Wnt /βcatenin信号通路是否被激活?:一项免疫组织化学研究

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Background: The loss of reduction of some adhesion molecules is associated with the invasive phenotype of carcinomas. The aim of this paper was to study the expression of some proteins related to the Wnt/β catenin signalling pathway in seminomas by immunohistochemical techniques in order to assess the contribution of this pathway to the tumoral development. Materials and Methods: Immunohistochemistry for E-cadherin, β-catenin, vimentin, C-Myc, cyclin D1 (CD1) and placental alkaline phosphatase. (PALP) was carried out in 24 archival tissue blocks of seminomas. Two cellular lines were used as E-cadherin and β-catenin controls. (JKT-1 and TCam-2). Results: E-cadherin was positive in two seminomas and in one carcinoma in situ. (CIS), showing a membranous pattern. βcatenin was principally expressed in Sertoli cells, in some malignant gonocytes of CIS and in the membranes of seminomatous cells. No β-catenin immunostaining was detectable in the cytoplasm and the nuclei of neoplastic cells. Seminomas were weakly possitive for vimentin in 11/24 cases. None of the tumors displayed expression of C-Myc or CD1. Conclusions: The results does not indicate the activation of the Wnt pathway, due to the lack of vimentin expression in 13/24 seminomas, the low expression in the rest of the cases, the lack of β-catenin in nuclei and the absence of CD1 and C-Myc expression. Further work is needed to confirm these observations and to test other signaling pathways in seminomas.
机译:背景:某些粘附分子减少的丧失与癌的浸润性表型有关。本文旨在通过免疫组织化学技术研究精原细胞瘤中与Wnt /βcatenin信号通路相关的某些蛋白质的表达,以评估该通路对肿瘤发展的贡献。材料和方法:免疫组织化学法检测E-钙粘蛋白,β-连环蛋白,波形蛋白,C-Myc,细胞周期蛋白D1(CD1)和胎盘碱性磷酸酶。 (PALP)在24例精原细胞存档组织块中进行。将两个细胞系用作E-钙粘蛋白和β-连环蛋白对照。 (JKT-1和TCam-2)。结果:E-钙黏着蛋白在两个精原细胞瘤和一个原位癌中呈阳性。 (CIS),呈膜状。 β-catenin主要表达于支持细胞,CIS的某些恶性性腺细胞和半裸细胞膜中。在肿瘤细胞的细胞质和细胞核中未检测到β-catenin免疫染色。在11/24例中,精原细胞瘤对波形蛋白的敏感性较弱。没有肿瘤显示出C-Myc或CD1的表达。结论:由于13/24精原细胞瘤中缺乏波形蛋白表达,其余病例表达低,细胞核中缺乏β-连环蛋白以及CD1缺失,因此该结果并未表明Wnt途径的激活。和C-Myc表达。需要进一步的工作来确认这些观察结果并测试精原细胞瘤中的其他信号通路。

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