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PMID: 7702605 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

c-erbB-2 gene product directly associates with beta-catenin and plakoglobin.

Biochemical and biophysical research communications ·Vol. 208 ·No. 3 ·1995-03-28 ·Pages 1067-72

Kanai Y, Ochiai A, Shibata T, Oyama T, Ushijima S, Akimoto S, Hirohashi S

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.

Related Genes
MeSH Terms
Adenocarcinoma Blotting, Western Cadherins/metabolism Cell Adhesion Molecules/metabolism Cloning, Molecular Cytoskeletal Proteins/isolation & purification,metabolism Desmoplakins ErbB Receptors Genes, erbB-2 Glutathione Transferase/biosynthesis,isolation & purification Humans Protein Binding Receptor, ErbB-2/biosynthesis,isolation & purification,metabolism Recombinant Fusion Proteins/biosynthesis,isolation & purification,metabolism Sequence Homology, Amino Acid Stomach Neoplasms Trans-Activators Tumor Cells, Cultured beta Catenin gamma Catenin
Chemicals
CTNNB1 protein, human Cadherins Cell Adhesion Molecules Cytoskeletal Proteins Desmoplakins Recombinant Fusion Proteins Trans-Activators beta Catenin gamma Catenin Glutathione Transferase ErbB Receptors Receptor, ErbB-2
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kanai Y
Pathology Division, National Cancer Center Research Institute, Tokyo, Japan.
Ochiai A
Shibata T
Oyama T
Ushijima S
Akimoto S
Hirohashi S
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1995-03-28
Pages
1067-72
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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