Abstract
Association of the c-erbB-2 oncogene product with the cadherin-catenin complex has been demonstrated in human cancer cell lines. Although beta-catenin and plakoglobin have been proven to be crucial for the association, no previous study has shown whether the interactions are direct or indirect. In the present study, the c-erbB-2 gene product was shown by far-Western blotting analysis to associate directly with both beta-catenin and plakoglobin through its cytoplasmic domain core region, which showed extensive homology with epidermal growth factor receptor. These data suggest that c-erbB-2-induced signaling is also directly liked to the cadherin-mediated cell adhesion and "invasion-suppressor" system through beta-catenin and plakoglobin in cancers.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenocarcinoma
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Blotting, Western
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Cadherins / metabolism
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Cell Adhesion Molecules / metabolism
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Cloning, Molecular
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Cytoskeletal Proteins / isolation & purification
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Cytoskeletal Proteins / metabolism*
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Desmoplakins
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ErbB Receptors
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Genes, erbB-2*
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Glutathione Transferase / biosynthesis
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Glutathione Transferase / isolation & purification
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Humans
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Protein Binding
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Receptor, ErbB-2 / biosynthesis
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Receptor, ErbB-2 / isolation & purification
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Receptor, ErbB-2 / metabolism*
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Recombinant Fusion Proteins / biosynthesis
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Recombinant Fusion Proteins / isolation & purification
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Recombinant Fusion Proteins / metabolism
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Sequence Homology, Amino Acid
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Stomach Neoplasms
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Trans-Activators*
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Tumor Cells, Cultured
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beta Catenin
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gamma Catenin
Substances
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CTNNB1 protein, human
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Cadherins
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Cell Adhesion Molecules
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Cytoskeletal Proteins
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Desmoplakins
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Recombinant Fusion Proteins
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Trans-Activators
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beta Catenin
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gamma Catenin
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Glutathione Transferase
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ErbB Receptors
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Receptor, ErbB-2