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Overexpression of Claudin-4 in Cholangiocarcinoma Tissues and its Possible Role in Tumor Metastasis

机译:Claudin-4在胆管癌组织中的过表达及其在肿瘤转移中的可能作用

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Claudin-4 (CLDN4) is a tight junction protein that forms apical junctional complexes in epithelial andendothelial cellular sheets. Acting as a barrier and control of permeability are the general functions of tightjunction proteins contributing to tissue homeostasis, paracellular ion flux, and cell-cell contact. In this study,we immunohistochemically examined CLDN4 expression in liver fluke-associated cholangiocarcinomas (CCAs)with tissue microarrays. Regardless of the histological type and gross type of cancer, high expression of CLDN4was noted in precancerous hyperplastic/dysplastic biliary epithelia and CCA. To investigate functional roles ofCLDN4 in cancer progression, the effects of CLDN4 suppression by siRNA on cell proliferation, migration andinvasion were investigated in two CCA cell lines, KKU-M139 and KKU-M213. Suppression of CLDN4 expressiondid not alter cell proliferation but caused significant reduction of cell migration and invasion by both CCA celllines. Our results suggest that over-expressed CLDN4 may promote CCA expansion and metastasis.
机译:Claudin-4(CLDN4)是紧密连接蛋白,可在上皮和内皮细胞层中形成顶端连接复合物。充当屏障和控制通透性的是紧密连接蛋白的一般功能,这些紧密连接蛋白可促进组织稳态,旁细胞离子通量和细胞接触。在这项研究中,我们用组织芯片免疫组化检查了在肝吸虫相关的胆管癌(CCA)中CLDN4的表达。不论癌的组织学类型和总体类型如何,在癌前增生/增生性胆管上皮细胞和CCA中均注意到CLDN4高表达。为了研究CLDN4在癌症进展中的功能作用,在两种CCA细胞系KKU-M139和KKU-M213中研究了siRNA抑制CLDN4对细胞增殖,迁移和侵袭的影响。 CLDN4表达的抑制并没有改变细胞增殖,但引起了两种CCA细胞株的细胞迁移和侵袭的显着减少。我们的结果表明,过表达的CLDN4可能会促进CCA的扩展和转移。

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