Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/61613

TitleBreast carcinomas that co-express E- and P-cadherin are associated with p120-catenin cytoplasmic localisation and poor patient survival
Author(s)Paredes, Joana
Correia, Ana Luisa
Ribeiro, Ana Sofia
Milanezi, Maria Fernanda Grillo
Cameselle-Teijeiro, J.
Schmitt, F. C.
KeywordsAdult
Aged
Aged, 80 and over
Biomarkers, Tumor
Breast Neoplasms
Cadherins
Catenins
Cytoplasm
Female
Humans
Membrane Proteins
Middle Aged
Neoplasm Invasiveness
Neoplasm Proteins
Survival Analysis
Issue dateJul-2008
PublisherBMJ Publishing Group
JournalJournal of Clinical Pathology
Abstract(s)Background: Changes in junctional catenin expression may compromise cadherin-mediated adhesion, increasing cell malignant properties such as invasive and metastatic abilities. Altered expression of alpha-, beta-, gamma- and p120-catenin has been reported to be associated with E-cadherin loss or decreased expression, in both breast carcinomas and breast cancer cell lines. Aims and Methods: To investigate the expression and subcellular localisation of p120- and beta-catenin in a series of human invasive breast carcinomas, and correlate it with biological markers and clinicopathological parameters. Results: Both catenins frequently exhibited a reduced membranous or cytoplasmic staining pattern. These alterations were significantly correlated with lack of both E-cadherin and oestrogen receptor-alpha expression. It was possible to associate the expression of beta-catenin with histological grade, tumour size and nodal status, suggesting a relevant role for this catenin as a prognostic factor. The majority of E- and P-cadherin co-expressing tumours were related to cytoplasmic expression of p120-catenin; in this group of breast carcinomas, patient survival was poor. Conclusion: Results indicate that p120-catenin cytoplasmic accumulation may play an important role in mediating the oncogenic effects derived from P-cadherin aberrant expression, including enhanced motility and invasion, particularly in tumours which maintain E-cadherin expression.
TypeArticle
URIhttp://hdl.handle.net/1822/61613
DOI10.1136/jcp.2007.052704
ISSN0021-9746
e-ISSN1472-4146
Peer-Reviewedyes
AccessRestricted access (Author)
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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