Gene interactions and pathways from curated databases and text-mining
Biochem Biophys Res Commun 1995, PMID: 7702605

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

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

  • 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