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Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies
In 66 breast cancer biopsies, the expression of the Ca(2+)-binding protein S100A4, E-cadherin, α- and β-catenin was examined by immunohistochemistry, and the results were related to clinical and pathological parameters. High levels of S100A4 were found to significantly correlate with histological gr...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408909/ https://www.ncbi.nlm.nih.gov/pubmed/12439718 http://dx.doi.org/10.1038/sj.bjc.6600624 |
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author | Pedersen, K B Nesland, J M Fodstad, Ø Mælandsmo, G M |
author_facet | Pedersen, K B Nesland, J M Fodstad, Ø Mælandsmo, G M |
author_sort | Pedersen, K B |
collection | PubMed |
description | In 66 breast cancer biopsies, the expression of the Ca(2+)-binding protein S100A4, E-cadherin, α- and β-catenin was examined by immunohistochemistry, and the results were related to clinical and pathological parameters. High levels of S100A4 were found to significantly correlate with histological grade (P=0.030) and loss of oestrogen receptor (P=0.046), but not to the time interval between surgery and development of distant metastasis (P=0.51) or to patient survival (P=0.89). Loss of E-cadherin expression, associated with altered cell–cell adhesion, showed a highly significant association to overall survival (P=0.020) and metastasis-free period (P=0.0052). In multivariate analysis, only lymph node involvement was a more significant predictor of patient demise. No association was found between expression of S100A4 and any single member of the cadherin–catenin complex, but a trend (P=0.053) towards reduced expression of one or several of these proteins and S100A4 immunoreactivity was observed. In conclusion, although our results suggest an association between S100A4 expression and an aggressive tumour phenotype, no relationship to overall survival was found. Deregulation of E-cadherin expression, however, was of high prognostic significance. British Journal of Cancer (2002) 87, 1281–1286. doi:10.1038/sj.bjc.6600624 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2408909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24089092009-09-10 Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies Pedersen, K B Nesland, J M Fodstad, Ø Mælandsmo, G M Br J Cancer Molecular and Cellular Pathology In 66 breast cancer biopsies, the expression of the Ca(2+)-binding protein S100A4, E-cadherin, α- and β-catenin was examined by immunohistochemistry, and the results were related to clinical and pathological parameters. High levels of S100A4 were found to significantly correlate with histological grade (P=0.030) and loss of oestrogen receptor (P=0.046), but not to the time interval between surgery and development of distant metastasis (P=0.51) or to patient survival (P=0.89). Loss of E-cadherin expression, associated with altered cell–cell adhesion, showed a highly significant association to overall survival (P=0.020) and metastasis-free period (P=0.0052). In multivariate analysis, only lymph node involvement was a more significant predictor of patient demise. No association was found between expression of S100A4 and any single member of the cadherin–catenin complex, but a trend (P=0.053) towards reduced expression of one or several of these proteins and S100A4 immunoreactivity was observed. In conclusion, although our results suggest an association between S100A4 expression and an aggressive tumour phenotype, no relationship to overall survival was found. Deregulation of E-cadherin expression, however, was of high prognostic significance. British Journal of Cancer (2002) 87, 1281–1286. doi:10.1038/sj.bjc.6600624 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-11-18 2002-11-12 /pmc/articles/PMC2408909/ /pubmed/12439718 http://dx.doi.org/10.1038/sj.bjc.6600624 Text en Copyright © 2002 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular and Cellular Pathology Pedersen, K B Nesland, J M Fodstad, Ø Mælandsmo, G M Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies |
title | Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies |
title_full | Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies |
title_fullStr | Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies |
title_full_unstemmed | Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies |
title_short | Expression of S100A4, E-cadherin, α- and β-catenin in breast cancer biopsies |
title_sort | expression of s100a4, e-cadherin, α- and β-catenin in breast cancer biopsies |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408909/ https://www.ncbi.nlm.nih.gov/pubmed/12439718 http://dx.doi.org/10.1038/sj.bjc.6600624 |
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