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High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression

BACKGROUND: Egr-1 (early growth response-1 transcription factor) has been proposed to be involved in invasion and metastasis processes of human bladder cancer, but Egr-1 protein expression levels in human bladder cancer have not been investigated. In the present study we investigated the expression...

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Autores principales: Egerod, Frederikke Lihme, Bartels, Annette, Fristrup, Niels, Borre, Michael, Ørntoft, Torben F, Oleksiewicz, Martin B, Brünner, Nils, Dyrskjøt, Lars
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774864/
https://www.ncbi.nlm.nih.gov/pubmed/19878561
http://dx.doi.org/10.1186/1471-2407-9-385
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author Egerod, Frederikke Lihme
Bartels, Annette
Fristrup, Niels
Borre, Michael
Ørntoft, Torben F
Oleksiewicz, Martin B
Brünner, Nils
Dyrskjøt, Lars
author_facet Egerod, Frederikke Lihme
Bartels, Annette
Fristrup, Niels
Borre, Michael
Ørntoft, Torben F
Oleksiewicz, Martin B
Brünner, Nils
Dyrskjøt, Lars
author_sort Egerod, Frederikke Lihme
collection PubMed
description BACKGROUND: Egr-1 (early growth response-1 transcription factor) has been proposed to be involved in invasion and metastasis processes of human bladder cancer, but Egr-1 protein expression levels in human bladder cancer have not been investigated. In the present study we investigated the expression levels of Egr-1 protein in early stages of human bladder cancer and correlated it to later progression. METHODS: Expression of Egr-1 protein in human bladder cancer was examined by immunohistochemistry, on a tissue microarray constructed from tumors from 289 patients with non-muscle invasive urothelial bladder cancer. RESULTS: The frequency of tumor cells with nuclear Egr-1 immunolabelling correlated to bladder cancer stage, grade and to later progression to muscle-invasive bladder cancer (T2-4). Stage T1 tumors exhibited significantly higher frequencies of tumor cells with nuclear Egr-1 immunolabelling than Ta tumors (P = 0.001). Furthermore, Kaplan-Meier survival analysis showed that a high frequency of tumor cells with nuclear Egr-1 immunolabelling was significantly associated with a higher risk of progression to stage T2-4 (log-rank test, P = 0.035). Tumor cells with nuclear Egr-1 immunolabelling were found to localize at the tumor front in some of the tumor biopsies. CONCLUSION: The results from this study support a potential involvement of Egr-1 in the progression from non-muscle invasive bladder cancers to muscle invasive bladder cancer.
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spelling pubmed-27748642009-11-10 High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression Egerod, Frederikke Lihme Bartels, Annette Fristrup, Niels Borre, Michael Ørntoft, Torben F Oleksiewicz, Martin B Brünner, Nils Dyrskjøt, Lars BMC Cancer Research Article BACKGROUND: Egr-1 (early growth response-1 transcription factor) has been proposed to be involved in invasion and metastasis processes of human bladder cancer, but Egr-1 protein expression levels in human bladder cancer have not been investigated. In the present study we investigated the expression levels of Egr-1 protein in early stages of human bladder cancer and correlated it to later progression. METHODS: Expression of Egr-1 protein in human bladder cancer was examined by immunohistochemistry, on a tissue microarray constructed from tumors from 289 patients with non-muscle invasive urothelial bladder cancer. RESULTS: The frequency of tumor cells with nuclear Egr-1 immunolabelling correlated to bladder cancer stage, grade and to later progression to muscle-invasive bladder cancer (T2-4). Stage T1 tumors exhibited significantly higher frequencies of tumor cells with nuclear Egr-1 immunolabelling than Ta tumors (P = 0.001). Furthermore, Kaplan-Meier survival analysis showed that a high frequency of tumor cells with nuclear Egr-1 immunolabelling was significantly associated with a higher risk of progression to stage T2-4 (log-rank test, P = 0.035). Tumor cells with nuclear Egr-1 immunolabelling were found to localize at the tumor front in some of the tumor biopsies. CONCLUSION: The results from this study support a potential involvement of Egr-1 in the progression from non-muscle invasive bladder cancers to muscle invasive bladder cancer. BioMed Central 2009-10-30 /pmc/articles/PMC2774864/ /pubmed/19878561 http://dx.doi.org/10.1186/1471-2407-9-385 Text en Copyright ©2009 Egerod 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 Article
Egerod, Frederikke Lihme
Bartels, Annette
Fristrup, Niels
Borre, Michael
Ørntoft, Torben F
Oleksiewicz, Martin B
Brünner, Nils
Dyrskjøt, Lars
High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression
title High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression
title_full High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression
title_fullStr High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression
title_full_unstemmed High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression
title_short High frequency of tumor cells with nuclear Egr-1 protein expression in human bladder cancer is associated with disease progression
title_sort high frequency of tumor cells with nuclear egr-1 protein expression in human bladder cancer is associated with disease progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774864/
https://www.ncbi.nlm.nih.gov/pubmed/19878561
http://dx.doi.org/10.1186/1471-2407-9-385
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