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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2003-01-01
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Series: | Analytical Cellular Pathology |
Online Access: | http://dx.doi.org/10.1155/2003/574829 |
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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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