The Journal of Pathology · 1998 · 118 citations · 22 references
MedicineDermatologyPathologyCell AdhesionHistologyHistopathologyHistopathology Of Skin TumorsMelanocytic LesionsMelanocytic TumorsNeoplastic Skin LesionsSkin TumorsTumor HistopathologyBenign Melanocytic LesionsBenign Melanocytic TumorsCalcium-dependent Cell AdhesionE-cadherin LossE-cadherin-mediated AdhesionHistopathological LesionsMalignant Melanocytic LesionsMalignant Melanocytic Tumors
E-cadherin is a calcium-dependent cell-cell adhesion molecule expressed by melanocytes and responsible for their adhesion to keratinocytes in vitro. In this study, the expression of E-cadherin and its associated cytoplasmic proteins alpha-, beta-, and gamma-catenin was evaluated in melanocytic lesions by immunohistochemistry. E-cadherin expression was evaluated in 70 malignant melanomas and the catenins in 35 of these specimens. Twenty benign melanocytic naevi were also evaluated for E-cadherin and catenin expression. In normal epidermis, E-cadherin/catenin immunostaining was localized at the intercellular borders. In melanomas, a differential loss of E-cadherin expression was observed. Membranous E-cadherin staining was absent in dermal nests of melanomas in their radial growth phase and in Clark level II and III lesions, whereas it was present in a high proportion of melanomas in their vertical growth phase, in Clark level IV and V lesions and in metastasizing melanomas. In contrast, superficial compartments of naevi showed membranous E-cadherin immunoreactivity and junctional naevus cell nests displayed heterogeneous or diffuse cytoplasmic staining. Cytoplasmic alpha- and beta-catenin, but not gamma-catenin staining were detected in all benign and malignant lesions. These findings indicate that qualitative changes in the expression and cellular localization of E-cadherin and of alpha-, beta-, and gamma-catenin occur in melanocytic lesions and may reflect different stages in their progression.
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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
Stabilization of β-Catenin by Genetic Defects in Melanoma Cell Lines
Bonnee Rubinfeld, Paul F. Robbins, Mona El‐Gamil et al. · Science · 1997 · 1.2K citations