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A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer

BACKGROUND: Treatment decisions in colorectal cancer subsequent to surgery are based mainly on the TNM system. There is a need to establish novel prognostic markers based on the molecular characterization of tumor cells. Evidence exists that sialyl Le(X) expression is correlated with an unfavorable...

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Autores principales: Schiffmann, Leif, Schwarz, Fabian, Linnebacher, Michael, Prall, Friedrich, Pahnke, Jens, Krentz, Helga, Vollmar, Brigitte, Klar, Ernst
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407720/
https://www.ncbi.nlm.nih.gov/pubmed/22621806
http://dx.doi.org/10.1186/1477-7819-10-95
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author Schiffmann, Leif
Schwarz, Fabian
Linnebacher, Michael
Prall, Friedrich
Pahnke, Jens
Krentz, Helga
Vollmar, Brigitte
Klar, Ernst
author_facet Schiffmann, Leif
Schwarz, Fabian
Linnebacher, Michael
Prall, Friedrich
Pahnke, Jens
Krentz, Helga
Vollmar, Brigitte
Klar, Ernst
author_sort Schiffmann, Leif
collection PubMed
description BACKGROUND: Treatment decisions in colorectal cancer subsequent to surgery are based mainly on the TNM system. There is a need to establish novel prognostic markers based on the molecular characterization of tumor cells. Evidence exists that sialyl Le(X) expression is correlated with an unfavorable outcome in colorectal cancer. The aim of this study was to establish a simple sialyl Le(X) staining score and to determine a potential correlation with the prognosis in a series of advanced colorectal carcinoma patients. METHODS: In order to implement routine use of sialyl Le(X) immunohistology, we established a new, easily reproducible score and defined a cutoff which discriminated groups with better or worse outcome, respectively. We then correlated sialyl Le(X) expression of 215 UICC stage III and IV patients with disease-free and cancer-related survival. RESULTS: A five-stage score could be established based on automated immunohistochemical stainings. Using a statistical model, we calculated a cutoff to discriminate between weak and strong staining positivity of sialyl Le(X). Patients with strong positive specimens had a worse cancer-related survival (P = 0.004) but no difference was observed for disease-free survival (P = 0.352). CONCLUSIONS: These results demonstrate a strong correlation between high sialyl Le(X)-expression in colorectal carcinomas and cancer-related survival. Our highly standardized and easy-to-use staining score is suitable for routine use and hence it could be recommended to evaluate sialyl Le(X)-expression as part of the standard histopathological analysis of colorectal carcinomas and to validate the score prospectively based on a larger population.
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spelling pubmed-34077202012-07-30 A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer Schiffmann, Leif Schwarz, Fabian Linnebacher, Michael Prall, Friedrich Pahnke, Jens Krentz, Helga Vollmar, Brigitte Klar, Ernst World J Surg Oncol Research BACKGROUND: Treatment decisions in colorectal cancer subsequent to surgery are based mainly on the TNM system. There is a need to establish novel prognostic markers based on the molecular characterization of tumor cells. Evidence exists that sialyl Le(X) expression is correlated with an unfavorable outcome in colorectal cancer. The aim of this study was to establish a simple sialyl Le(X) staining score and to determine a potential correlation with the prognosis in a series of advanced colorectal carcinoma patients. METHODS: In order to implement routine use of sialyl Le(X) immunohistology, we established a new, easily reproducible score and defined a cutoff which discriminated groups with better or worse outcome, respectively. We then correlated sialyl Le(X) expression of 215 UICC stage III and IV patients with disease-free and cancer-related survival. RESULTS: A five-stage score could be established based on automated immunohistochemical stainings. Using a statistical model, we calculated a cutoff to discriminate between weak and strong staining positivity of sialyl Le(X). Patients with strong positive specimens had a worse cancer-related survival (P = 0.004) but no difference was observed for disease-free survival (P = 0.352). CONCLUSIONS: These results demonstrate a strong correlation between high sialyl Le(X)-expression in colorectal carcinomas and cancer-related survival. Our highly standardized and easy-to-use staining score is suitable for routine use and hence it could be recommended to evaluate sialyl Le(X)-expression as part of the standard histopathological analysis of colorectal carcinomas and to validate the score prospectively based on a larger population. BioMed Central 2012-05-23 /pmc/articles/PMC3407720/ /pubmed/22621806 http://dx.doi.org/10.1186/1477-7819-10-95 Text en Copyright ©2012 Schiffmann 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
Schiffmann, Leif
Schwarz, Fabian
Linnebacher, Michael
Prall, Friedrich
Pahnke, Jens
Krentz, Helga
Vollmar, Brigitte
Klar, Ernst
A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer
title A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer
title_full A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer
title_fullStr A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer
title_full_unstemmed A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer
title_short A novel sialyl Le(X) expression score as a potential prognostic tool in colorectal cancer
title_sort novel sialyl le(x) expression score as a potential prognostic tool in colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407720/
https://www.ncbi.nlm.nih.gov/pubmed/22621806
http://dx.doi.org/10.1186/1477-7819-10-95
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