Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer

Expression of MCAM is observed in a variety of human malignancies. We aimed to determine the rate of MCAM expression in our non‐small cell lung cancer (NSCLC) collection and to clarify its correlation with clinicopathological parameters and patient survival. 85 NSCLC were analysed immunohistochemica...

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Main Authors: Glen Kristiansen, Yongwei Yu, Karsten Schlüns, Christine Sers, Manfred Dietel, Iver Petersen
Format: Article
Language:English
Published: Hindawi Limited 2003-01-01
Series:Analytical Cellular Pathology
Online Access:http://dx.doi.org/10.1155/2003/574829
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spelling doaj-a67762c7d8e1420597c2164e711b91892020-11-25T01:11:39ZengHindawi LimitedAnalytical Cellular Pathology0921-89121878-36512003-01-01252778110.1155/2003/574829Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung CancerGlen Kristiansen0Yongwei Yu1Karsten Schlüns2Christine Sers3Manfred Dietel4Iver Petersen5Institute of Pathology, Charité University Hospital, 10117 Berlin, GermanyInstitute of Pathology, Charité University Hospital, 10117 Berlin, GermanyInstitute of Pathology, Charité University Hospital, 10117 Berlin, GermanyInstitute of Pathology, Charité University Hospital, 10117 Berlin, GermanyInstitute of Pathology, Charité University Hospital, 10117 Berlin, GermanyInstitute of Pathology, Charité University Hospital, 10117 Berlin, GermanyExpression of MCAM is observed in a variety of human malignancies. We aimed to determine the rate of MCAM expression in our non‐small cell lung cancer (NSCLC) collection and to clarify its correlation with clinicopathological parameters and patient survival. 85 NSCLC were analysed immunohistochemically using a monoclonal MCAM antibody (clone N1238) on an NSCLC tissue micro array. The staining was semiquantitatively scored. We found MCAM expression in 51% of NSCLC, preferentially squamous cell carcinomas (p=0.004). No other correlations to tumour size, grade, or stage were found. Univariate survival analysis showed no significant differences of MCAM positive and negative tumours. In adenocarcinomas however, MCAM positivity was significantly associated with shorter patient survival (p=0.016). We conclude, that MCAM is expressed in a high proportion of NSCLC and might be predictive of shortened patient survival in adenocarcinomas of the lung. Colour figure can be viewed on http://www.esacp.org/acp/2003/25-2/kristiansen.htm.http://dx.doi.org/10.1155/2003/574829
collection DOAJ
language English
format Article
sources DOAJ
author Glen Kristiansen
Yongwei Yu
Karsten Schlüns
Christine Sers
Manfred Dietel
Iver Petersen
spellingShingle Glen Kristiansen
Yongwei Yu
Karsten Schlüns
Christine Sers
Manfred Dietel
Iver Petersen
Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer
Analytical Cellular Pathology
author_facet Glen Kristiansen
Yongwei Yu
Karsten Schlüns
Christine Sers
Manfred Dietel
Iver Petersen
author_sort Glen Kristiansen
title Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer
title_short Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer
title_full Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer
title_fullStr Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer
title_full_unstemmed Expression of the Cell Adhesion Molecule CD146/MCAM in Non-Small Cell Lung Cancer
title_sort expression of the cell adhesion molecule cd146/mcam in non-small cell lung cancer
publisher Hindawi Limited
series Analytical Cellular Pathology
issn 0921-8912
1878-3651
publishDate 2003-01-01
description Expression of MCAM is observed in a variety of human malignancies. We aimed to determine the rate of MCAM expression in our non‐small cell lung cancer (NSCLC) collection and to clarify its correlation with clinicopathological parameters and patient survival. 85 NSCLC were analysed immunohistochemically using a monoclonal MCAM antibody (clone N1238) on an NSCLC tissue micro array. The staining was semiquantitatively scored. We found MCAM expression in 51% of NSCLC, preferentially squamous cell carcinomas (p=0.004). No other correlations to tumour size, grade, or stage were found. Univariate survival analysis showed no significant differences of MCAM positive and negative tumours. In adenocarcinomas however, MCAM positivity was significantly associated with shorter patient survival (p=0.016). We conclude, that MCAM is expressed in a high proportion of NSCLC and might be predictive of shortened patient survival in adenocarcinomas of the lung. Colour figure can be viewed on http://www.esacp.org/acp/2003/25-2/kristiansen.htm.
url http://dx.doi.org/10.1155/2003/574829
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