Q. Lan et al., Glutathione S-transferase genotypes and stomach cancer in a population-based case-control study in Warsaw, Poland, PHARMACOGEN, 11(8), 2001, pp. 655-661
Glutathione S-transferases are important in the detoxification of a wide ra
nge of human carcinogens. Previous studies have shown inconsistent associat
ions between the GSTT1 and GSTM1 null genotypes and stomach cancer risk. We
investigated the relationship between these and related genotypes and stom
ach cancer risk in a population-based case-control study in Warsaw, Poland,
where stomach cancer incidence and mortality rates are among the highest i
n Europe. DNA from blood samples was available for 304 stomach cancer patie
nts and 427 control subjects. We observed a 1.48-fold increased risk for st
omach cancer (95% confidence interval 0.97-2.25) in patients with the GSTT1
null genotype but no evidence of increased risk associated with the GSTM1,
GSTM3 or GSTP1 genotypes. Furthermore, the stomach cancer risk associated
with the GSTT1 null genotype varied by age at diagnosis, with odds ratios o
f 3.85, 1.91, 1.78 and 0.59 for those diagnosed at ages less than 50, 50-59
, 60-69 and 70 years or older, respectively (P trend = 0.01). This was due
to a shift in the GSTT1 genotype distribution across age groups among stoma
ch cancer patients only. These results suggest that the GSTT1 null genotype
may be associated with increased risk of stomach cancer. Pharmacogenetics
11:655-661 (C) 2001 Lippincott Williams & Wilkins.