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- and ß-Catenin Genes in Human Gastric and Breast Carcinomas
GSF-Forschungszentrum für Umwelt und Gesundheit, Institut für Pathologie, Neuherberg, Postfach 11 29, D-85758 Oberschleissheim [S. C., P. B., K-F. B., H. H.], and Institut für Pathologie der Technischen Universität, Klinikum rechts der Isar, Ismaningerstrasse 22, D-81675 München [H. H.], Germany
Disturbed function of E-cadherin and/or of one of its anchoring proteins, the catenins, is thought to destabilize E-cadherin-mediated cell-cell adhesion, which may enhance the invasiveness of epithelial cells and thus favor carcinoma progression. Reduced expression of E-cadherin and
-catenin, as well as mutations in the E-cadherin gene, have been found in various carcinomas, whereas mutations in the
- and ß-catenin genes have been described only in carcinoma cell lines. Using reverse transcription-PCR, followed by agarose gel electrophoresis and single-strand conformational polymorphism, we examined 16 diffuse- and 5 intestinal-type gastric carcinomas, as well as 9 lobular and 2 ductal breast carcinomas, for mutations of
- and ß-catenin cDNA. All of the investigated tumors were analyzed previously for E-cadherin mutations. Comparing tumorous and nontumorous samples, we detected neither deletions nor aberrant single-strand conformational polymorphism patterns. At nucleotide 2220 of the
-catenin gene, we identified one frequent polymorphism. Our findings suggest that, in contrast to E-cadherin, mutations of
- and ß-catenin do not contribute to the pathogenesis or the diffuse growth patterns of gastric or breast carcinomas.
1 To whom requests for reprints should be addressed.
Received 9/18/95. Accepted 11/14/95.
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