PubMed · 2010 · 30 citations · 27 references
MedicineGynecologyPathologyCarcinogenesisCell AdhesionNeoplasiaEndometrial BiopsyEndometrial CancerEpithelial TumorsNeoplastic PathophysiologyUterine PathologyAtrophic EndometriumAtypical Endometrial HyperplasiaE-cadherin-mediated AdhesionEndometrial ProliferationNeoplastic DiseaseNeoplastic ProgressionRepresentative Samples
UNLABELLED: The aim of this study was to determine whether modulation of expression of cell adhesion molecules may occur in neoplastic transformation of endometrial epithelium. MATERIALS AND METHODS: E-Cadherin and α-catenin protein expression were evaluated by immunohistochemistry in 124 biopsies representative of normal, hyperplastic and neoplastic endometrium. RESULTS: In normal endometrium (proliferative, secretive and atrophic endometrium) strong homogeneous, E-cadherin and α-catenin reactivity was found; 58.3% and 66.6% of biopsies representative of simple hyperplastic endometrium were homogeneously positive for E-cadherin and α-catenin, respectively, whereas no samples representative of atypical hyperplasia showed evidence of homogeneous E-cadherin or α-catenin expression. No expression of homogeneous E-cadherin was seen in endometrial adenocarcinomas; α-catenin homogeneous immunostaining was observed in 2 G1 and 2 G2 out of 22 adenocarcinoma samples (18.2%). A homogeneous co-expression of both molecules was seen only in normal (70%) and simple hyperplastic (46%) endometrium. CONCLUSION: These results suggest that E-cadherin and α-catenin down-regulation might be associated with neoplastic transformation of endometrial tissues.
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E-cadherin-mediated cell-cell adhesion prevents invasiveness of human carcinoma cells.
U. Frixen, Jürgen Behrens, Matthew S. Sachs et al. · The Journal of Cell Biology · 1991 · 1.6K citations · Full text
Medicine, Cell Biology, Oncology +17
R. W. Noyes, Arthur T. Hertig, John A. Rock · American Journal of Obstetrics and Gynecology · 1975 · 953 citations
Medicine, Gynecology, Pathology +7