Back to Search Start Over

Data from N-acetyltransferase 2 Phenotype, Occupation, and Bladder Cancer Risk: Results from the EPIC Cohort

Authors :
Paolo Vineis
Thomas Brüning
Elio Riboli
Isabelle Romieu
Pietro Ferrari
Timothy J. Key
Nick Wareham
Kay-Tee Khaw
Roy Ehrnström
David Ulmert
Mattias Johansson
Börje Ljungberg
Aurelio Barricarte
Carmen Navarro
Miren Dorronsoro
Mariá José Sánchez
Carlos González
José Ramón Quirós
Salvatore Panico
Rosario Tumino
Sabina Sieri
Domenico Palli
Dimitrios Trichopoulos
Steffen Weikert
Heiner Boeing
Laure Dossus
Marie-Christine Boutron-Ruault
Françoise Clavel-Chapelon
Kim Overvad
Anne Tjønneland
Nina Roswall
Jenny Chang-Claude
Rudolf Kaaks
Martine M. Ros
Bas Bueno-de-Mesquita
Norman Klopp
Thomas Illig
Jürgen Angerer
Hui Ding
Hans-Peter Rihs
Swaantje Casjens
Tobias Weiss
Sylvia Rabstein
Katarzyna Gawrych
Beate Pesch
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

Abstract

Background: An association between N-acetyltransferase 2 (NAT2) slow acetylation and bladder cancer has been consistently observed in epidemiologic studies. However, evidence has been mainly derived from case–control studies and was sparse from cohort studies. We evaluated the association between NAT2 slow acetylation and bladder cancer in a case–control study nested in the European Prospective Investigation into Cancer and Nutrition.Methods: Exposure to aromatic amines and polycyclic aromatic hydrocarbons (PAH) could be assessed for 754 cases and 833 controls for whom occupational information was documented. A semiquantitative job-exposure matrix was applied to at-risk occupations to estimate the exposure as low, medium, or high based on tertiles of the distribution of the exposure score in controls. Using a comprehensive genotyping, NAT2 acetylation status could be categorized from 6-single-nucleotide polymorphism genotypes as slow or fast in 607 cases and 695 controls with DNA from archived blood samples.Results: Occupational exposure to aromatic amines and PAH was associated with an increased bladder cancer risk [upper tertile of the distribution of the exposure score: OR = 1.37; 95% confidence interval (CI), 1.02–1.84, and OR = 1.50; 95% CI, 1.09–2.05, respectively]. NAT2 slow acetylation did not modify these risk estimates and was not itself associated with bladder cancer risk (OR = 1.02; 95% CI, 0.81–1.29).Conclusions: These findings confirm established or suspected occupational risk factors but not the anticipated role of NAT2 slow acetylation in bladder cancer. No interaction was detected between NAT2 and any exposure of interest, including smoking.Impact: Genetic testing for NAT2 would be inappropriate in occupational settings. Cancer Epidemiol Biomarkers Prev; 22(11); 2055–65. ©2013 AACR.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....7cd0f9059d7b3c40a93c869c092e3ad6