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N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction
Genetic polymorphism of the carcinogen metabolizing enzyme N -acetyl transferase 2 (NAT2) may influence susceptibility to bladder cancers related to smoking or to occupational exposure to arylamine carcinogens. This article reviews the results of 21 published case–control studies of NAT2 polymorphis...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374558/ https://www.ncbi.nlm.nih.gov/pubmed/10917561 http://dx.doi.org/10.1054/bjoc.2000.1265 |
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author | Green, J Banks, E Berrington, A Darby, S Deo, H Newton, R |
author_facet | Green, J Banks, E Berrington, A Darby, S Deo, H Newton, R |
author_sort | Green, J |
collection | PubMed |
description | Genetic polymorphism of the carcinogen metabolizing enzyme N -acetyl transferase 2 (NAT2) may influence susceptibility to bladder cancers related to smoking or to occupational exposure to arylamine carcinogens. This article reviews the results of 21 published case–control studies of NAT2 polymorphism and bladder-cancer risk, with a total of 2700 cases and 3426 controls. The published evidence suggests that NAT2 slow acetylator phenotype or genotype may be associated with a small increase in bladder cancer risk. However, given the possibility of selective publication of results from studies that found an excess risk, the current evidence is not sufficient to conclude that there is a real increase in risk. Only five of the 21 studies reported results separately for the effect of NAT2 on bladder cancer risk in smokers and non-smokers. Although the results suggest that the effect may be greater in smokers than in non-smokers, the possibility of publication bias makes these results difficult to interpret. There was insufficient evidence to assess the joint effect of NAT2 and occupational exposure to arylamines on bladder cancer risk. Even if estimates of the effect of NAT2 from published data are correct, studies with around 3000–5000 cases will be needed to confirm them. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23745582009-09-10 N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction Green, J Banks, E Berrington, A Darby, S Deo, H Newton, R Br J Cancer Regular Article Genetic polymorphism of the carcinogen metabolizing enzyme N -acetyl transferase 2 (NAT2) may influence susceptibility to bladder cancers related to smoking or to occupational exposure to arylamine carcinogens. This article reviews the results of 21 published case–control studies of NAT2 polymorphism and bladder-cancer risk, with a total of 2700 cases and 3426 controls. The published evidence suggests that NAT2 slow acetylator phenotype or genotype may be associated with a small increase in bladder cancer risk. However, given the possibility of selective publication of results from studies that found an excess risk, the current evidence is not sufficient to conclude that there is a real increase in risk. Only five of the 21 studies reported results separately for the effect of NAT2 on bladder cancer risk in smokers and non-smokers. Although the results suggest that the effect may be greater in smokers than in non-smokers, the possibility of publication bias makes these results difficult to interpret. There was insufficient evidence to assess the joint effect of NAT2 and occupational exposure to arylamines on bladder cancer risk. Even if estimates of the effect of NAT2 from published data are correct, studies with around 3000–5000 cases will be needed to confirm them. © 2000 Cancer Research Campaign Nature Publishing Group 2000-07 2000-07-03 /pmc/articles/PMC2374558/ /pubmed/10917561 http://dx.doi.org/10.1054/bjoc.2000.1265 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Green, J Banks, E Berrington, A Darby, S Deo, H Newton, R N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
title | N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
title_full | N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
title_fullStr | N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
title_full_unstemmed | N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
title_short | N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
title_sort | n-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene–environment interaction |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374558/ https://www.ncbi.nlm.nih.gov/pubmed/10917561 http://dx.doi.org/10.1054/bjoc.2000.1265 |
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