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Título

E-cadherin missense mutations, associated with hereditary diffuse gastric cancer (HDGC) syndrome, display distinct invasive behaviors and genetic interactions with the Wnt and Notch pathways in Drosophila epithelia

AutorPereira, Paulo S.; Teixeira, Alexandra; Pinho, Sofia; Ferreira, Paulo; Fernández, Joana; Seruca, Raquel; Suriano, Gianpaolo; Casares, Fernando
Palabras claveArmadillo domain proteins
Cadherins
Drosophila
Epithelium
Neoplastic syndromes
Stomach neoplasms
Wnt proteins
Beta catenin
Fecha de publicación16-abr-2006
EditorOxford University Press
CitaciónHuman Molecular Genetics 15(10): 1704-1712 (2006)
ResumenGermline mutations in the human E-cadherin (hEcad) gene, CDH1, are initiating events in cases of human hereditary diffuse gastric cancer (HDGC) indicating that hEcad is a tumor suppressor. Among the hEcad mutations identified so far, some are missense, but the pathological relevance of these missense mutants is still unclear. In vitro assays show that missense mutations result in full-length hEcad molecules that retain some distinct biological activity, but in vivo functional studies in animal models are still lacking. Here we verify the potential of a Drosophila model to in vivo characterize the functional consequences of HDGC-associated germline missense mutations and to identify signaling pathways affected by these mutations. To this end, we have generated transgenic fly strains expressing the wild-type hEcad gene or its missense mutations. Similar to the fly Ecad, expression of wild-type hEcad and missense forms in fly epithelia resulted in their localization to the subapical region. In addition, we verify a genotype-phenotype correlation associated to the specific domain affected by the mutations, because cells expressing normal or missense mutant hEcad display different migratory and invasive behaviors in fly epithelia. We show that some of these effects might be mediated through hEcad interacting with the endogenous fly ss-catenin, Armadillo, thus interfering with the Wnt signaling pathway. Therefore, the use of this simple in vivo system will contribute to characterize the effects that missense hEcad have on cell behavior in a tissue environment, and might help to understand their significance in gastric cancer onset.
Descripción9 páginas, 6 figuras.
Versión del editorhttp://dx.doi.org/10.1093/hmg/ddl093
URIhttp://hdl.handle.net/10261/41364
DOI10.1093/hmg/ddl093
ISSN0964-6906
E-ISSN1460-2083
ReferenciasPMID: 16600987
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