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Distinct Claudin Expression Profiles of Hepatocellular Carcinoma and Metastatic Colorectal and Pancreatic Carcinomas

机译:肝细胞癌转移性结直肠癌和胰腺癌的截然不同的Claudin表达谱

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摘要

Tight junction proteins, including claudins, are often dysregulated during carcinogenesis and tumor progression. Moreover, the claudin expression pattern usually varies between different tumor entities. We aimed to investigate claudin expression profiles of primary and metastatic liver malignancies. We analyzed claudin-1, -2, -3, -4, and -7 expression by quantitative immunohistochemistry and real-time RT-PCR, respectively. Twenty hepatocellular carcinomas (HCCs) and liver metastases of 20 colorectal adenocarcinomas (CRLMs) and 15 pancreatic adenocarcinomas (PLMs) were studied together with paired surrounding non-tumorous liver samples and 5 normal liver samples. Strong claudin-3 and -7 immunohistochemical positivities were detected in CRLM samples, each with significantly stronger staining when compared with HCC and PLM groups. Claudin-1 protein was found highly expressed in CRLM, in contrast to lower expression in PLM and HCC. CRLMs and PLMs also were strongly positive for claudin-4, while being virtually undetectable in HCC. Claudin-2 showed strong positivity in non-tumorous liver tissue, whereas significantly weaker positivity was observed in all tumors. Differences in mRNA expression were mostly similar to those found by immunohistochemistry. In conclusion, HCC and both CRLM and PLM display distinct claudin expression profiles, which might provide better understanding of the pathobiology of these lesions and might be used for differential diagnosis.
机译:致密连接蛋白,包括claudins,在致癌和肿瘤发展过程中常常失调。而且,claudin表达模式通常在不同的肿瘤实体之间变化。我们旨在调查原发性和转移性肝恶性肿瘤的claudin表达谱。我们通过定量免疫组织化学和实时RT-PCR分别分析了claudin-1,-2,-3,-4和-7的表达。研究了20例肝细胞癌(HCC)和20例大肠腺癌(CRLM)和15例胰腺腺癌(PLM)的肝转移以及周围成对的非肿瘤肝样品和5例正常肝样品。在CRLM样品中检测到了强claudin-3和-7免疫组化阳性,与HCC和PLM组相比,每个染色均具有明显更强的染色性。发现Claudin-1蛋白在CRLM中高表达,而在PLM和HCC中较低。 CRLM和PLM也对claudin-4呈强阳性,而在HCC中几乎未检出。 Claudin-2在非肿瘤肝组织中显示出较强的阳性,而在所有肿瘤中均观察到明显较弱的阳性。 mRNA表达的差异与免疫组织化学发现的相似。总之,HCC以及CRLM和PLM均显示出独特的claudin表达谱,这可能会更好地了解这些病变的病理生物学特性,并可用于鉴别诊断。

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