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E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.

Reduced expression of E-cadherin, a Ca(2+)-dependent cell adhesion molecule present in normal epithelium, has been associated with invasive and metastatic cancer. Immunohistochemistry was used in examining the relationship between E-cadherin expression and stage in 59 oesophageal and 52 lung cancers...

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Autores principales: Bongiorno, P. F., al-Kasspooles, M., Lee, S. W., Rachwal, W. J., Moore, J. H., Whyte, R. I., Orringer, M. B., Beer, D. G.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033452/
https://www.ncbi.nlm.nih.gov/pubmed/7819034
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author Bongiorno, P. F.
al-Kasspooles, M.
Lee, S. W.
Rachwal, W. J.
Moore, J. H.
Whyte, R. I.
Orringer, M. B.
Beer, D. G.
author_facet Bongiorno, P. F.
al-Kasspooles, M.
Lee, S. W.
Rachwal, W. J.
Moore, J. H.
Whyte, R. I.
Orringer, M. B.
Beer, D. G.
author_sort Bongiorno, P. F.
collection PubMed
description Reduced expression of E-cadherin, a Ca(2+)-dependent cell adhesion molecule present in normal epithelium, has been associated with invasive and metastatic cancer. Immunohistochemistry was used in examining the relationship between E-cadherin expression and stage in 59 oesophageal and 52 lung cancers. Advanced-stage oesophageal cancers were associated with both reduced and disorganised E-cadherin expression (P < 0.01). Advanced-stage lung adenocarcinomas generally exhibited disorganised or reduced E-cadherin expression, but no statistical association between expression pattern and stage was found (P > 0.05). No differences in stage were seen between tumours with reduced or disorganised E-cadherin expression. Altered E-cadherin expression was detected in dysplastic, non-invasive Barrett's oesophagus. Importantly, high-level E-cadherin expression was detected in 17 of 17 lymph nodes containing metastatic cancer. E-cadherin mRNA expression was decreased in tumours with reduced protein expression, but not in tumours with disorganised expression. Expression of alpha-catenin mRNA, an E-cadherin-associated protein, was detected in tissues with altered E-cadherin protein expression. Reduced and disorganised expression of E-cadherin appear to be related to transcriptional and post-translational events respectively, and both appear to represent altered cell adhesion associated with invasion and metastasis in thoracic neoplasms. IMAGES:
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spelling pubmed-20334522009-09-10 E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus. Bongiorno, P. F. al-Kasspooles, M. Lee, S. W. Rachwal, W. J. Moore, J. H. Whyte, R. I. Orringer, M. B. Beer, D. G. Br J Cancer Research Article Reduced expression of E-cadherin, a Ca(2+)-dependent cell adhesion molecule present in normal epithelium, has been associated with invasive and metastatic cancer. Immunohistochemistry was used in examining the relationship between E-cadherin expression and stage in 59 oesophageal and 52 lung cancers. Advanced-stage oesophageal cancers were associated with both reduced and disorganised E-cadherin expression (P < 0.01). Advanced-stage lung adenocarcinomas generally exhibited disorganised or reduced E-cadherin expression, but no statistical association between expression pattern and stage was found (P > 0.05). No differences in stage were seen between tumours with reduced or disorganised E-cadherin expression. Altered E-cadherin expression was detected in dysplastic, non-invasive Barrett's oesophagus. Importantly, high-level E-cadherin expression was detected in 17 of 17 lymph nodes containing metastatic cancer. E-cadherin mRNA expression was decreased in tumours with reduced protein expression, but not in tumours with disorganised expression. Expression of alpha-catenin mRNA, an E-cadherin-associated protein, was detected in tissues with altered E-cadherin protein expression. Reduced and disorganised expression of E-cadherin appear to be related to transcriptional and post-translational events respectively, and both appear to represent altered cell adhesion associated with invasion and metastasis in thoracic neoplasms. IMAGES: Nature Publishing Group 1995-01 /pmc/articles/PMC2033452/ /pubmed/7819034 Text en 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 Research Article
Bongiorno, P. F.
al-Kasspooles, M.
Lee, S. W.
Rachwal, W. J.
Moore, J. H.
Whyte, R. I.
Orringer, M. B.
Beer, D. G.
E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.
title E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.
title_full E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.
title_fullStr E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.
title_full_unstemmed E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.
title_short E-cadherin expression in primary and metastatic thoracic neoplasms and in Barrett's oesophagus.
title_sort e-cadherin expression in primary and metastatic thoracic neoplasms and in barrett's oesophagus.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033452/
https://www.ncbi.nlm.nih.gov/pubmed/7819034
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