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PMID: 9522220 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of E-cadherin, alpha-catenin and beta-catenin in normal ovarian surface epithelium and epithelial ovarian cancers.

Histopathology ·Vol. 32 ·No. 1 ·1998-01-00 ·Pages 69-80

Davies BR, Worsley SD, Ponder BA

Abstract

To study the expression of the epithelial adhesion molecule E-cadherin and its associated proteins alpha and beta catenin in paraffin sections of normal ovaries, benign cystadenomas and ovarian carcinomas, and in immortalized normal ovarian surface epithelial cells and ovarian carcinoma cells in culture. Immunocytochemistry was used to study expression of the proteins in paraffin sections and western blotting was used to determine levels of expression of the proteins in cell extracts. E-cadherin expression was found to be absent in ovarian surface epithelial cells in culture and infrequently expressed in normal ovarian surface epithelial cells in vivo, although apical punctate staining was occasionally seen. Seven of nine benign cystadenomas and 29/34 epithelial ovarian carcinomas showed some expression of E-cadherin, but expression was absent in poorly differentiated tumours. Expression of alpha and beta catenin was consistently detected on the lateral membranes of normal ovarian epithelium and benign cystadenomas. alpha and beta catenin expression was lost in 18% and 21% of ovarian carcinomas, respectively: other ovarian carcinomas expressed these proteins at a reduced level. A small number of these tumours showed a diffuse cytoplasmic rather than membranous staining. Reduced staining for alpha and beta catenin appeared to correlate with a more spindly, less adhesive morphology and increased invasive potential in matrigel. The results suggest that E-cadherin expression is generally induced in well differentiated ovarian cancers. In contrast, alpha and beta catenins are consistently expressed in the normal ovarian surface epithelium and benign tumours, but are sometimes reduced or absent in ovarian carcinomas. It is likely that the catenins associate with membrane proteins other than E-cadherin in ovarian epithelium, and they may possibly function as tumour suppressors in this epithelium.

MeSH Terms
Animals Cadherins/metabolism Cell Adhesion Molecules/metabolism Cell Line Cytoskeletal Proteins/metabolism Epithelium/chemistry,metabolism,pathology Female Humans Immunohistochemistry Neoplasm Invasiveness Ovarian Neoplasms/chemistry,metabolism Ovary/chemistry,metabolism Trans-Activators Tumor Cells, Cultured alpha Catenin beta Catenin
Chemicals
CTNNA1 protein, human CTNNB1 protein, human Cadherins Cell Adhesion Molecules Cytoskeletal Proteins Trans-Activators alpha Catenin beta Catenin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Davies B R
WellBeing Ovarian Cancer Research Centre, University of Cambridge, Addenbrookes Hospital, UK.
Worsley S D
Ponder B A
Article Info
Journal
Histopathology
Abbr.
Histopathology
ISSN
0309-0167
Published
1998-01-00
Pages
69-80
Language
English
Region
England
NLM ID
7704136
Subset
IM
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