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Significance of EpCAM and TROP2 expression in non-small cell lung cancer

BACKGROUND: The tumor-associated calcium signal transducer (TACSTD) genes, originally designated epithelial cell adhesion molecule (EpCAM) and TROP2, represent true oncogenes. Little is known about EpCAM and TROP2 gene expression in non-small cell lung carcinoma (NSCLC). This study evaluated EpCAM a...

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Autores principales: Pak, Min Gyoung, Shin, Dong Hoon, Lee, Chang Hun, Lee, Min Ki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342122/
https://www.ncbi.nlm.nih.gov/pubmed/22482828
http://dx.doi.org/10.1186/1477-7819-10-53
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author Pak, Min Gyoung
Shin, Dong Hoon
Lee, Chang Hun
Lee, Min Ki
author_facet Pak, Min Gyoung
Shin, Dong Hoon
Lee, Chang Hun
Lee, Min Ki
author_sort Pak, Min Gyoung
collection PubMed
description BACKGROUND: The tumor-associated calcium signal transducer (TACSTD) genes, originally designated epithelial cell adhesion molecule (EpCAM) and TROP2, represent true oncogenes. Little is known about EpCAM and TROP2 gene expression in non-small cell lung carcinoma (NSCLC). This study evaluated EpCAM and TROP2 protein expression and clinicopathologic significance in cases of NSCLC. METHODS: Tissue microarray blocks acquired from 164 cases of NSCLC, including 100 cases of adenocarcinoma (AdC) and 64 of squamous cell carcinoma (SCC), were examined by immunohistochemical staining for EpCAM, and TROP2. The results were correlated with clinicopathologic data. RESULTS: EpCAM and TROP2 were significantly overexpressed in SCC than in AdC (P < 0.01). In AdC, EpCAM overexpression was closely related to sex, histologic grade, pathologic T stage, pathologic N stage, and TNM stage, and TROP2 overexpression was only related to histologic grade (P < 0.05, respectively). In SCC, correlations were evident between EpCAM overexpression and TNM stage (P = 0.01), and between TROP2 overexpression and pathologic T stage (P = 0.02). EpCAM overexpression showed no significance with overall survival in AdC and SCC patients. However, TROP2 overexpression in AdC had a positive influence on overall survival (P = 0.02) and disease-free survival (P = 0.03). In particular, AdC patients with stage II or III showed better overall survival (P = 0.05) and disease-free survival (P = 0.04). CONCLUSIONS: While EpCAM and TROP2 show weak and non-complete membranous staining in normal bronchial epithelium and pneumocyte, their complete membranous expression in carcinoma suggests their role in carcinogenesis. EpCAM and TROP2 were more frequently overexpressed in SCC. EpCAM overexpression had no prognostic value in this study, but TROP2 overexpression showed better survival in AdC patients and might be a better prognostic marker in advanced stage AdC.
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spelling pubmed-33421222012-05-03 Significance of EpCAM and TROP2 expression in non-small cell lung cancer Pak, Min Gyoung Shin, Dong Hoon Lee, Chang Hun Lee, Min Ki World J Surg Oncol Research BACKGROUND: The tumor-associated calcium signal transducer (TACSTD) genes, originally designated epithelial cell adhesion molecule (EpCAM) and TROP2, represent true oncogenes. Little is known about EpCAM and TROP2 gene expression in non-small cell lung carcinoma (NSCLC). This study evaluated EpCAM and TROP2 protein expression and clinicopathologic significance in cases of NSCLC. METHODS: Tissue microarray blocks acquired from 164 cases of NSCLC, including 100 cases of adenocarcinoma (AdC) and 64 of squamous cell carcinoma (SCC), were examined by immunohistochemical staining for EpCAM, and TROP2. The results were correlated with clinicopathologic data. RESULTS: EpCAM and TROP2 were significantly overexpressed in SCC than in AdC (P < 0.01). In AdC, EpCAM overexpression was closely related to sex, histologic grade, pathologic T stage, pathologic N stage, and TNM stage, and TROP2 overexpression was only related to histologic grade (P < 0.05, respectively). In SCC, correlations were evident between EpCAM overexpression and TNM stage (P = 0.01), and between TROP2 overexpression and pathologic T stage (P = 0.02). EpCAM overexpression showed no significance with overall survival in AdC and SCC patients. However, TROP2 overexpression in AdC had a positive influence on overall survival (P = 0.02) and disease-free survival (P = 0.03). In particular, AdC patients with stage II or III showed better overall survival (P = 0.05) and disease-free survival (P = 0.04). CONCLUSIONS: While EpCAM and TROP2 show weak and non-complete membranous staining in normal bronchial epithelium and pneumocyte, their complete membranous expression in carcinoma suggests their role in carcinogenesis. EpCAM and TROP2 were more frequently overexpressed in SCC. EpCAM overexpression had no prognostic value in this study, but TROP2 overexpression showed better survival in AdC patients and might be a better prognostic marker in advanced stage AdC. BioMed Central 2012-04-06 /pmc/articles/PMC3342122/ /pubmed/22482828 http://dx.doi.org/10.1186/1477-7819-10-53 Text en Copyright ©2012 Pak et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Pak, Min Gyoung
Shin, Dong Hoon
Lee, Chang Hun
Lee, Min Ki
Significance of EpCAM and TROP2 expression in non-small cell lung cancer
title Significance of EpCAM and TROP2 expression in non-small cell lung cancer
title_full Significance of EpCAM and TROP2 expression in non-small cell lung cancer
title_fullStr Significance of EpCAM and TROP2 expression in non-small cell lung cancer
title_full_unstemmed Significance of EpCAM and TROP2 expression in non-small cell lung cancer
title_short Significance of EpCAM and TROP2 expression in non-small cell lung cancer
title_sort significance of epcam and trop2 expression in non-small cell lung cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342122/
https://www.ncbi.nlm.nih.gov/pubmed/22482828
http://dx.doi.org/10.1186/1477-7819-10-53
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