Modulation of urinary mutagenicity by genetically determined carcinogen metabolism in smokers.

Abstract:

:We examined the genotypes of two polymorphic genes involved in the detoxification of several mutagenic and carcinogenic compounds in relation to tobacco smoking-associated urinary mutagenicity. The genes studied were the glutathione S-transferase-encoding GSTM1 gene and acetyltransferase-encoding NAT2 gene. Smokers with no GSTM1 gene (n = 7) had urine that was several times more mutagenic than that of smokers with the gene (n = 10). The mean level of urinary mutagenicity in presence of metabolic activation was 2527 +/- 958 revertants/100 ml urine for GSTM1-smokers compared to 766 +/- 560 revertants/100 ml for GSTM1+ smokers (P < 0.001) using the bacterial strain YG1024. The corresponding values using the TA98 strain were 336 +/- 124 and 123 +/- 75 (P < 0.001). In contrast, we failed to show any difference in the level of urinary mutagenicity between slow-acetylator and fast-acetylator NAT2 genotypes among smokers (n = 17) or non-smokers (n = 35). Our results offer one explanation for the recent findings that GSTM1 polymorphism is a risk modifier in smoking-related cancers, especially bladder cancer.

journal_name

Carcinogenesis

journal_title

Carcinogenesis

authors

Hirvonen A,Nylund L,Kociba P,Husgafvel-Pursiainen K,Vainio H

doi

10.1093/carcin/15.5.813

subject

Has Abstract

pub_date

1994-05-01 00:00:00

pages

813-5

issue

5

eissn

0143-3334

issn

1460-2180

journal_volume

15

pub_type

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