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Abnormal expression and function of the E-cadherin-catenin complex in gastric carcinoma cell lines.

Abstract
Dysfunction of the cadherin-catenin complex, a key component of adherens junctions, is thought to confer invasive potential to cells. The aim of this study is to examine the expression and function of the E-cadherin/catenin complex in gastric carcinoma cell lines. Expression of E-cadherin, alpha, beta and gamma-catenin and p120ctn, and of the adenomatous polyposis coli protein (APC), together with function of the cadherin-catenin complex was examined in a panel of gastric carcinoma cell lines, using immunocytochemistry, Western blotting and a cell-cell aggregation assay. Protein interactions were examined by sequential immunoprecipitation and immunoblotting with antibodies to E-cadherin, alpha, beta and gamma-catenin, p120ctn and APC. Abnormalities of E-cadherin, alpha- and beta-catenin expression, were associated with disturbance of E-cadherin-catenin complex composition, loss of membranous localization and loss of calcium-dependent aggregation in six gastric carcinoma cell lines. APC protein expression and interaction with beta-catenin was preserved in five cell lines. We demonstrate frequent abnormalities of expression and function of E-cadherin and catenins, and associated disturbance of E-cadherin-mediated intercellular adhesion in gastric carcinoma cell lines. These findings support the tumour suppressor role of the E-cadherin and its contribution to the development and progression of the neoplastic phenotype in gastric carcinoma.
AuthorsA U Jawhari, M Noda, M J Farthing, M Pignatelli
JournalBritish journal of cancer (Br J Cancer) Vol. 80 Issue 3-4 Pg. 322-30 (May 1999) ISSN: 0007-0920 [Print] England
PMID10408833 (Publication Type: Journal Article)
Chemical References
  • CTNNA1 protein, human
  • CTNNB1 protein, human
  • CTNNB1 protein, mouse
  • Cadherins
  • Ctnna1 protein, mouse
  • Cytoskeletal Proteins
  • Macromolecular Substances
  • Trans-Activators
  • alpha Catenin
  • beta Catenin
Topics
  • Animals
  • Cadherins (biosynthesis, metabolism, physiology)
  • Carcinoma (metabolism, pathology)
  • Cell Adhesion (physiology)
  • Cell Aggregation (physiology)
  • Cell Communication (physiology)
  • Cytoskeletal Proteins (biosynthesis, metabolism, physiology)
  • Humans
  • Macromolecular Substances
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Stomach Neoplasms (metabolism, pathology)
  • Trans-Activators
  • Tumor Cells, Cultured
  • alpha Catenin
  • beta Catenin

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