TY - JOUR
T1 - N-acetyltransferase 2 and bladder cancer
T2 - An overview and consideration of the evidence for gene-environment interaction
AU - Green, J.
AU - Banks, E.
AU - Berrington, A.
AU - Darby, S.
AU - Deo, H.
AU - Newton, R.
PY - 2000
Y1 - 2000
N2 - 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. (C) 2000 Cancer Research Campaign.
AB - 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. (C) 2000 Cancer Research Campaign.
KW - Arylamines
KW - Bladder cancer
KW - Gene-environment interaction
KW - Genetic polymorphism
KW - NAT2
KW - Smoking
UR - http://www.scopus.com/inward/record.url?scp=0033938764&partnerID=8YFLogxK
U2 - 10.1054/bjoc.2000.1265
DO - 10.1054/bjoc.2000.1265
M3 - Article
SN - 0007-0920
VL - 83
SP - 412
EP - 417
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 3
ER -