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β4 and β6 Integrin Expression Is Associated with the Subclassification and Clinicopathological Features of Intrahepatic Cholangiocarcinoma

机译:β4和β6整联蛋白表达与肝内胆管癌的子类化和临床病理特征有关

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摘要

Intrahepatic cholangiocarcinoma (ICC) is a heterogeneous group of cancers of the intrahepatic biliary tract. However, few studies have evaluated integrin expression according to an ICC subgroup. We immunohistochemically investigated α6β4 (β4) and αvβ6 (β6) integrin expressions in 48 ICCs, and evaluated their relationship with clinical and pathological parameters and ligand expression, as well as transforming growth factor (TGF)-β1. β4 and β6 expressions were detected in 46 (96%) and 35 (73%) ICC cases, respectively. We classified ICC into negative, low (β4, 29 cases; β6, 36 cases), or high (β4, 19 cases; β6, 12 cases) integrin expression groups. β4 and β6 integrin levels were higher in the non-peripheral central localization type ICC than in the peripheral localization type; they were also higher in the periductal-infiltrating or intraductal-growth types than in the mass-forming type ICC; lastly, they were higher in the well-differentiated type than in the poorly-differentiated type ICC. High expression was related to bile duct invasion. In addition, β4 and β6 expressions were associated with mucin production and the expression of cytoplasmic epithelial membrane antigen, laminin-5, and tenascin-C. TGF-β1 was correlated with β6 expression and poor overall survival. These results suggest that integrin expression is associated with subclassification and clinicopathological features of ICC through the coincident expression of their ligands and TGF-β1.
机译:肝内胆管癌(ICC)是肝内胆道的异质癌。然而,很少有研究根据ICC子组评估整联蛋白表达。我们研究了免疫组织化学α6β4(β4)和联蛋白αvβ6(β6)整合表达的IC卡48,并评价它们与临床和病理参数和配体表达的关系,以及转化生长因子(TGF)-β1。在46(96%)和35(73%)ICC病例中检测β4和β6表达。我们将ICC分为阴性,低(β4,29例;β6,36例)或高(β4,19例;β6,12例)整合蛋白表达组。非外围中央定位类型ICC中的β4和β6整合蛋白水平高于外围定位类型;它们的潜水渗透或内含性生长类型也比在成磅形成型ICC中更高;最后,它们的良好分化的类型较高,而不是在差异差异的ICC中。高表达与胆管侵袭有关。此外,β4和β6表达与粘蛋白产生和细胞质上皮膜抗原,层压蛋白-5和Tenascin-C的表达有关。 TGF-β1与β6表达和整体存活差相关。这些结果表明,整联蛋白表达与ICC的副分类和临床病理特征与其配体和TGF-β1的一致表达相关。

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