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Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer

BACKGROUND: Tumor-specific biomarkers are a prerequisite for the development of targeted imaging and therapy in oral squamous cell carcinoma (OSCC). urokinase-type Plasminogen Activator Receptor (uPAR), Tissue Factor (TF) and Epidermal Growth Factor Receptor (EGFR) are three biomarkers that exhibit...

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Autores principales: Christensen, Anders, Kiss, Katalin, Lelkaitis, Giedrius, Juhl, Karina, Persson, Morten, Charabi, Birgitte Wittenborg, Mortensen, Jann, Forman, Julie Lyng, Sørensen, Anne Lyngholm, Jensen, David Hebbelstrup, Kjaer, Andreas, von Buchwald, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574145/
https://www.ncbi.nlm.nih.gov/pubmed/28841839
http://dx.doi.org/10.1186/s12885-017-3563-3
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author Christensen, Anders
Kiss, Katalin
Lelkaitis, Giedrius
Juhl, Karina
Persson, Morten
Charabi, Birgitte Wittenborg
Mortensen, Jann
Forman, Julie Lyng
Sørensen, Anne Lyngholm
Jensen, David Hebbelstrup
Kjaer, Andreas
von Buchwald, Christian
author_facet Christensen, Anders
Kiss, Katalin
Lelkaitis, Giedrius
Juhl, Karina
Persson, Morten
Charabi, Birgitte Wittenborg
Mortensen, Jann
Forman, Julie Lyng
Sørensen, Anne Lyngholm
Jensen, David Hebbelstrup
Kjaer, Andreas
von Buchwald, Christian
author_sort Christensen, Anders
collection PubMed
description BACKGROUND: Tumor-specific biomarkers are a prerequisite for the development of targeted imaging and therapy in oral squamous cell carcinoma (OSCC). urokinase-type Plasminogen Activator Receptor (uPAR), Tissue Factor (TF) and Epidermal Growth Factor Receptor (EGFR) are three biomarkers that exhibit enhanced expression in many types of cancers, and have been investigated as potential biomarkers for targeted strategies and prognostication. The aim of the study was to investigate the expression patterns of uPAR, TF and EGFR and their potential prognostic value in OSCC. METHODS: Immunohistochemical expression of uPAR, TF and EGFR in tumor resection specimens from 191 patients with primary OSCC was analyzed. Overall (OS) and disease-free survival (DFS) was calculated. Associations between biomarker expression, clinicopathological factors and patient survival was analyzed using the Cox proportional hazards model for univariate and multivariate analysis, log rank and Kaplan-Meier statistics. RESULTS: uPAR and TF exhibited a highly tumor-specific expression pattern while EGFR also showed expression in normal tissues outside the tumor compartment. The overall positive expression rate of uPAR, TF and EGFR was 95%, 58% and 98%, respectively. High uPAR expression across the entire cohort was negatively associated with OS (p = 0.031, HR = 1.595 (95%CI 1.044–2.439)) in univariate analysis. The 5-year OS for high and low uPAR expression was 39% and 56%, respectively. The expression of TF and EGFR was not associated with survival outcome. CONCLUSIONS: This study may suggest that uPAR and TF could potentially be attractive targets for molecular imaging and therapy in OSCC due to high positive expression rates and tumor-specific expression patterns. High uPAR expression was significantly associated with a reduced survival. uPAR seems to be a prognostic biomarker in oral cancer.
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spelling pubmed-55741452017-08-30 Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer Christensen, Anders Kiss, Katalin Lelkaitis, Giedrius Juhl, Karina Persson, Morten Charabi, Birgitte Wittenborg Mortensen, Jann Forman, Julie Lyng Sørensen, Anne Lyngholm Jensen, David Hebbelstrup Kjaer, Andreas von Buchwald, Christian BMC Cancer Research Article BACKGROUND: Tumor-specific biomarkers are a prerequisite for the development of targeted imaging and therapy in oral squamous cell carcinoma (OSCC). urokinase-type Plasminogen Activator Receptor (uPAR), Tissue Factor (TF) and Epidermal Growth Factor Receptor (EGFR) are three biomarkers that exhibit enhanced expression in many types of cancers, and have been investigated as potential biomarkers for targeted strategies and prognostication. The aim of the study was to investigate the expression patterns of uPAR, TF and EGFR and their potential prognostic value in OSCC. METHODS: Immunohistochemical expression of uPAR, TF and EGFR in tumor resection specimens from 191 patients with primary OSCC was analyzed. Overall (OS) and disease-free survival (DFS) was calculated. Associations between biomarker expression, clinicopathological factors and patient survival was analyzed using the Cox proportional hazards model for univariate and multivariate analysis, log rank and Kaplan-Meier statistics. RESULTS: uPAR and TF exhibited a highly tumor-specific expression pattern while EGFR also showed expression in normal tissues outside the tumor compartment. The overall positive expression rate of uPAR, TF and EGFR was 95%, 58% and 98%, respectively. High uPAR expression across the entire cohort was negatively associated with OS (p = 0.031, HR = 1.595 (95%CI 1.044–2.439)) in univariate analysis. The 5-year OS for high and low uPAR expression was 39% and 56%, respectively. The expression of TF and EGFR was not associated with survival outcome. CONCLUSIONS: This study may suggest that uPAR and TF could potentially be attractive targets for molecular imaging and therapy in OSCC due to high positive expression rates and tumor-specific expression patterns. High uPAR expression was significantly associated with a reduced survival. uPAR seems to be a prognostic biomarker in oral cancer. BioMed Central 2017-08-25 /pmc/articles/PMC5574145/ /pubmed/28841839 http://dx.doi.org/10.1186/s12885-017-3563-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Christensen, Anders
Kiss, Katalin
Lelkaitis, Giedrius
Juhl, Karina
Persson, Morten
Charabi, Birgitte Wittenborg
Mortensen, Jann
Forman, Julie Lyng
Sørensen, Anne Lyngholm
Jensen, David Hebbelstrup
Kjaer, Andreas
von Buchwald, Christian
Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer
title Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer
title_full Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer
title_fullStr Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer
title_full_unstemmed Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer
title_short Urokinase-type plasminogen activator receptor (uPAR), tissue factor (TF) and epidermal growth factor receptor (EGFR): tumor expression patterns and prognostic value in oral cancer
title_sort urokinase-type plasminogen activator receptor (upar), tissue factor (tf) and epidermal growth factor receptor (egfr): tumor expression patterns and prognostic value in oral cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574145/
https://www.ncbi.nlm.nih.gov/pubmed/28841839
http://dx.doi.org/10.1186/s12885-017-3563-3
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