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Asian Pac J Cancer Prev ; 13(2): 677-81, 2012.
Article in English | MEDLINE | ID: mdl-22524844

ABSTRACT

The aim of the present research was to investigate clinicopathologic correlations of immunohistochemically- demonstrated axin (axis inhibition) and ß-catenin expression in primary hepatocellular carcinomas (HCCs), in comparison with paraneoplastic, cirrhotic and normal liver tissues. Variation in Axin expression across groups were significant (P < 0.01), correlating with alpha fetoprotein (AFP), HBsAg, cancer plugs in the portal vein, and clinical stage of HCCs(P < 0.05); however, there were no links with sex, age, and tumour size (P > 0.05). Differences in cell membrane ß-catenin expression were also statistically significant (P < 0.01), again correlated with AFP, HBsAg, cancer plugs in the portal vein, and clinical stage in HCCs (P < 0.05) but not with sex, age, and tumour size (P > 0.05). Axin expression levels in tissues with reduced membrane ß-catenin were low (P < 0.05), also being low with nuclear ß-catenin expression (P < 0.05). Axin and ß-catenin may play an important role in the genesis and progression of HCC via the Wnt signal transmission pathway. Simultaneous determination of axin, ß-catenin, AFP, and HBsAg may be useful for early diagnosis, and metastatic and clinical staging of HCCs.


Subject(s)
Axin Protein/metabolism , Biomarkers, Tumor/metabolism , Carcinoma, Hepatocellular/metabolism , Liver Neoplasms/metabolism , beta Catenin/metabolism , Adult , Aged , Carcinoma, Hepatocellular/secondary , Case-Control Studies , Cell Membrane/metabolism , Female , Gene Expression Regulation, Neoplastic , Hepatitis B Surface Antigens/metabolism , Humans , Immunoenzyme Techniques , Liver/metabolism , Liver Cirrhosis/metabolism , Liver Cirrhosis/pathology , Liver Neoplasms/pathology , Male , Middle Aged , Neoplasm Staging , Portal Vein/metabolism , Portal Vein/pathology , Prognosis , alpha-Fetoproteins/metabolism
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