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      Somatic mutations of the beta-catenin gene are frequent in mouse and human hepatocellular carcinomas.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Base Sequence, Calcium-Calmodulin-Dependent Protein Kinases, metabolism, Carcinoma, Hepatocellular, genetics, pathology, Cytoskeletal Proteins, DNA Primers, Glycogen Synthase Kinase 3, Humans, Liver Neoplasms, Mice, Mice, Transgenic, Phosphorylation, Point Mutation, Trans-Activators, Tumor Cells, Cultured, beta Catenin

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          Abstract

          Hepatocellular carcinoma (HCC) is the major primary malignant tumor in the human liver, but the molecular changes leading to liver cell transformation remain largely unknown. The Wnt-beta-catenin pathway is activated in colon cancers and some melanoma cell lines, but has not yet been investigated in HCC. We have examined the status of the beta-catenin gene in different transgenic mouse lines of HCC obtained with the oncogenes c-myc or H-ras. Fifty percent of the hepatic tumors in these transgenic mice had activating somatic mutations within the beta-catenin gene similar to those found in colon cancers and melanomas. These alterations in the beta-catenin gene (point mutations or deletions) lead to a disregulation of the signaling function of beta-catenin and thus to carcinogenesis. We then analyzed human HCCs and found similar mutations in eight of 31 (26%) human liver tumors tested and in HepG2 and HuH6 hepatoma cells. The mutations led to the accumulation of beta-catenin in the nucleus. Thus alterations in the beta-catenin gene frequently are selected for during liver tumorigenesis and suggest that disregulation of the Wnt-beta-catenin pathway is a major event in the development of HCC in humans and mice.

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