Biochem Biophys Res Commun 1995,
PMID: 7702605
Kanai, Y; Ochiai, A; Shibata, T; Oyama, T; Ushijima, S; Akimoto, S; Hirohashi, S
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.
Diseases/Pathways annotated by Medline MESH: Adenocarcinoma, Stomach Neoplasms
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Text Mining Data
Dashed line = No text mining data
Manually curated Databases
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IRef Biogrid Interaction:
JUP
—
ERBB2
(direct interaction, far western blotting)
-
IRef Biogrid Interaction:
CTNNB1
—
ERBB2
(direct interaction, far western blotting)
-
IRef Biogrid Interaction:
CTNNB1
—
ERBB2
(direct interaction, pull down)
-
IRef Hprd Interaction:
JUP
—
ERBB2
(in vivo)
-
IRef Hprd Interaction:
JUP
—
ERBB2
(in vitro)
-
IRef Hprd Interaction:
CTNNB1
—
ERBB2
(in vitro)
-
IRef Hprd Interaction:
CTNNB1
—
ERBB2
(in vivo)
In total, 2 gene pairs are associated to this article in curated databases