Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis

Objectives. The inescapable relationship between chronic inflammation and carcinogenesis has long been established. Our objective was to investigate COX-2 and NF-𝜅B immunohistochemical expression in a large series of normal epithelium and bladder carcinomas. Methods. Immunohistochemical methodology...

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Main Authors: Stylianos Kontos, Georgia Sotiropoulou-Bonikou, Athina Kominea, Maria Melachrinou, Eleni Balampani, Dionysis Bonikos
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Advances in Urology
Online Access:http://dx.doi.org/10.1155/2010/871356
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author Stylianos Kontos
Georgia Sotiropoulou-Bonikou
Athina Kominea
Maria Melachrinou
Eleni Balampani
Dionysis Bonikos
author_facet Stylianos Kontos
Georgia Sotiropoulou-Bonikou
Athina Kominea
Maria Melachrinou
Eleni Balampani
Dionysis Bonikos
author_sort Stylianos Kontos
collection DOAJ
description Objectives. The inescapable relationship between chronic inflammation and carcinogenesis has long been established. Our objective was to investigate COX-2 and NF-𝜅B immunohistochemical expression in a large series of normal epithelium and bladder carcinomas. Methods. Immunohistochemical methodology was performed on formalin-fixed, paraffin-embedded sections from urinary bladder carcinomas of 140 patients (94 males and 46 females with bladder carcinomas). Results. COX-2 expression is increased in the cytoplasm of bladder cells, during loss of cell differentiation (𝑟s=0.61, 𝑃-value<.001) and in muscle invasive carcinomas (𝑃-value<.001). A strong positive association between tumor grade and nuclear expression of NF𝜅B has been established. A positive correlation between COX-2 and nuclear NF𝜅B immunoreactivity was observed. Conclusions. The possible coordinated upregulation of NF𝜅B and COX-2, during bladder carcinogenesis, indicates that agents inhibitors of these two molecules may represent a possible new treatment strategy, by virtue of their role in bladder carcinogenesis.
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institution Kabale University
issn 1687-6369
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language English
publishDate 2010-01-01
publisher Wiley
record_format Article
series Advances in Urology
spelling doaj-art-7a580ac4dc044b5eb7e00e2c81885d972025-02-03T06:08:27ZengWileyAdvances in Urology1687-63691687-63772010-01-01201010.1155/2010/871356871356Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder CarcinogenesisStylianos Kontos0Georgia Sotiropoulou-Bonikou1Athina Kominea2Maria Melachrinou3Eleni Balampani4Dionysis Bonikos5Department of Pathology, Medical School, University of Patras, 26504 Rion, GreeceDepartment of Anatomy and Histology-Embryology, Medical School, University of Patras, 26504 Rion, GreeceDepartment of Pathology, Aegion General Hospital, 25100 Aegion, GreeceDepartment of Pathology, Medical School, University of Patras, 26504 Rion, GreeceDepartment of Microbiology, General Hospital of Nikaia, 18543 Peiraeus, GreeceDepartment of Pathology, Medical School, University of Patras, 26504 Rion, GreeceObjectives. The inescapable relationship between chronic inflammation and carcinogenesis has long been established. Our objective was to investigate COX-2 and NF-𝜅B immunohistochemical expression in a large series of normal epithelium and bladder carcinomas. Methods. Immunohistochemical methodology was performed on formalin-fixed, paraffin-embedded sections from urinary bladder carcinomas of 140 patients (94 males and 46 females with bladder carcinomas). Results. COX-2 expression is increased in the cytoplasm of bladder cells, during loss of cell differentiation (𝑟s=0.61, 𝑃-value<.001) and in muscle invasive carcinomas (𝑃-value<.001). A strong positive association between tumor grade and nuclear expression of NF𝜅B has been established. A positive correlation between COX-2 and nuclear NF𝜅B immunoreactivity was observed. Conclusions. The possible coordinated upregulation of NF𝜅B and COX-2, during bladder carcinogenesis, indicates that agents inhibitors of these two molecules may represent a possible new treatment strategy, by virtue of their role in bladder carcinogenesis.http://dx.doi.org/10.1155/2010/871356
spellingShingle Stylianos Kontos
Georgia Sotiropoulou-Bonikou
Athina Kominea
Maria Melachrinou
Eleni Balampani
Dionysis Bonikos
Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis
Advances in Urology
title Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis
title_full Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis
title_fullStr Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis
title_full_unstemmed Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis
title_short Coordinated Increased Expression of Cyclooxygenase2 and Nuclear Factor 𝜅B Is a Steady Feature of Urinary Bladder Carcinogenesis
title_sort coordinated increased expression of cyclooxygenase2 and nuclear factor 𝜅b is a steady feature of urinary bladder carcinogenesis
url http://dx.doi.org/10.1155/2010/871356
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AT georgiasotiropouloubonikou coordinatedincreasedexpressionofcyclooxygenase2andnuclearfactorκbisasteadyfeatureofurinarybladdercarcinogenesis
AT athinakominea coordinatedincreasedexpressionofcyclooxygenase2andnuclearfactorκbisasteadyfeatureofurinarybladdercarcinogenesis
AT mariamelachrinou coordinatedincreasedexpressionofcyclooxygenase2andnuclearfactorκbisasteadyfeatureofurinarybladdercarcinogenesis
AT elenibalampani coordinatedincreasedexpressionofcyclooxygenase2andnuclearfactorκbisasteadyfeatureofurinarybladdercarcinogenesis
AT dionysisbonikos coordinatedincreasedexpressionofcyclooxygenase2andnuclearfactorκbisasteadyfeatureofurinarybladdercarcinogenesis