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Urinary human polyomavirus and papillomavirus infection and bladder cancer risk

BACKGROUND: The association of transitional cell carcinomas of the bladder (TCB) with Schistosoma haematobium suggested a possible role of infections in the aetiology of TCB. METHODS: In all, 114 TCB cases and 140 hospital controls from Pordenone Province were enrolled within an Italian multi-centri...

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Autores principales: Polesel, J, Gheit, T, Talamini, R, Shahzad, N, Lenardon, O, Sylla, B, La Vecchia, C, Serraino, D, Tommasino, M, Franceschi, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251864/
https://www.ncbi.nlm.nih.gov/pubmed/22116302
http://dx.doi.org/10.1038/bjc.2011.519
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author Polesel, J
Gheit, T
Talamini, R
Shahzad, N
Lenardon, O
Sylla, B
La Vecchia, C
Serraino, D
Tommasino, M
Franceschi, S
author_facet Polesel, J
Gheit, T
Talamini, R
Shahzad, N
Lenardon, O
Sylla, B
La Vecchia, C
Serraino, D
Tommasino, M
Franceschi, S
author_sort Polesel, J
collection PubMed
description BACKGROUND: The association of transitional cell carcinomas of the bladder (TCB) with Schistosoma haematobium suggested a possible role of infections in the aetiology of TCB. METHODS: In all, 114 TCB cases and 140 hospital controls from Pordenone Province were enrolled within an Italian multi-centric case–control study. Urine samples were screened for DNA from five human polyomaviruses (HPyV) (JCV, BKV, MCV, WUV, and KIV); SV40; and 22 mucosal human papillomaviruses (HPV) using highly sensitive PCR assays. Odds ratios (ORs) and corresponding confidence intervals (CIs) were computed for risk of TCB by HPyV- or HPV-positivity using unconditional logistic regression. RESULTS: Human polyomavirus prevalence was similar in TCB cases (71.7%) and controls (77.7%) (OR for TCB=0.85; 95% CI: 0.45–1.61). JCV was the most frequently detected HPyV type. No individual HPyV showed a significant association. Among cases, HPyV-positivity was not associated with tumour characteristics, but it was significantly lower in women than men and among current and former smokers than never smokers. Human papillomavirus was detected in seven cases and five controls (OR=1.52; 95% CI: 0.42–5.45). CONCLUSION: The present small study does not support an involvement of HPyV or HPV infection in TCB aetiology in immunocompetent individuals. Differences in HPyV-positivity by sex and smoking may derive from differences in either acquisition or persistence of the infection.
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spelling pubmed-32518642013-01-03 Urinary human polyomavirus and papillomavirus infection and bladder cancer risk Polesel, J Gheit, T Talamini, R Shahzad, N Lenardon, O Sylla, B La Vecchia, C Serraino, D Tommasino, M Franceschi, S Br J Cancer Epidemiology BACKGROUND: The association of transitional cell carcinomas of the bladder (TCB) with Schistosoma haematobium suggested a possible role of infections in the aetiology of TCB. METHODS: In all, 114 TCB cases and 140 hospital controls from Pordenone Province were enrolled within an Italian multi-centric case–control study. Urine samples were screened for DNA from five human polyomaviruses (HPyV) (JCV, BKV, MCV, WUV, and KIV); SV40; and 22 mucosal human papillomaviruses (HPV) using highly sensitive PCR assays. Odds ratios (ORs) and corresponding confidence intervals (CIs) were computed for risk of TCB by HPyV- or HPV-positivity using unconditional logistic regression. RESULTS: Human polyomavirus prevalence was similar in TCB cases (71.7%) and controls (77.7%) (OR for TCB=0.85; 95% CI: 0.45–1.61). JCV was the most frequently detected HPyV type. No individual HPyV showed a significant association. Among cases, HPyV-positivity was not associated with tumour characteristics, but it was significantly lower in women than men and among current and former smokers than never smokers. Human papillomavirus was detected in seven cases and five controls (OR=1.52; 95% CI: 0.42–5.45). CONCLUSION: The present small study does not support an involvement of HPyV or HPV infection in TCB aetiology in immunocompetent individuals. Differences in HPyV-positivity by sex and smoking may derive from differences in either acquisition or persistence of the infection. Nature Publishing Group 2012-01-03 2011-11-24 /pmc/articles/PMC3251864/ /pubmed/22116302 http://dx.doi.org/10.1038/bjc.2011.519 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Epidemiology
Polesel, J
Gheit, T
Talamini, R
Shahzad, N
Lenardon, O
Sylla, B
La Vecchia, C
Serraino, D
Tommasino, M
Franceschi, S
Urinary human polyomavirus and papillomavirus infection and bladder cancer risk
title Urinary human polyomavirus and papillomavirus infection and bladder cancer risk
title_full Urinary human polyomavirus and papillomavirus infection and bladder cancer risk
title_fullStr Urinary human polyomavirus and papillomavirus infection and bladder cancer risk
title_full_unstemmed Urinary human polyomavirus and papillomavirus infection and bladder cancer risk
title_short Urinary human polyomavirus and papillomavirus infection and bladder cancer risk
title_sort urinary human polyomavirus and papillomavirus infection and bladder cancer risk
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251864/
https://www.ncbi.nlm.nih.gov/pubmed/22116302
http://dx.doi.org/10.1038/bjc.2011.519
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