GSTT1 and GSTM1 null genotypes and the risk of gastric cancer: A case-control study in a Chinese population

Citation
Vw. Setiawan et al., GSTT1 and GSTM1 null genotypes and the risk of gastric cancer: A case-control study in a Chinese population, CANC EPID B, 9(1), 2000, pp. 73-80
Citations number
41
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
ISSN journal
10559965 → ACNP
Volume
9
Issue
1
Year of publication
2000
Pages
73 - 80
Database
ISI
SICI code
1055-9965(200001)9:1<73:GAGNGA>2.0.ZU;2-4
Abstract
Glutathione S-tranferase (GST) enzymes are involved in detoxification of ma ny potentially carcinogenic compounds. The homozygous deletions or null gen otypes of GSTT1 (theta class) and GSTM1 (mu class) genes may be associated with an increased risk of cancer. Few studies have evaluated the relationsh ip between GSTT1, GSTM1 and the risk of gastric cancer, as well as the pote ntial interactions between these genetic markers and other risk factors of gastric cancer in the Chinese population. We conducted a case-control study with 143 cases with gastric cancer, 166 chronic gastritis (CG) cases and 4 33 cancer-free population controls from Yangzhong County, China, The epidem iological data were collected by a standard questionnaire for all of the su bjects, and blood samples were obtained from 91 gastric cancer cases, 146 C G cases, and 429 controls. GSTT1 and GSTM1 genotypes were assayed by the PC R method, and Helicobacter pylori infection was measured by the ELISA metho d. Using logistic regression model in SAS, we assessed the independent effe cts of GSTT1 and GSTM1 null genotypes on the risk of gastric cancer and the ir potential interactions with other factors, The prevalence of GSTM1 null genotype was 48% in gastric cancer cases, 60% in CG patients, and 51% in co ntrols, The prevalence of GSTT1 null genotype was 54% in gastric cancer cas es, 48% in CG patients, and 46% in controls. After controlling for age, gen der, education, pack-years of smoking, alcohol drinking, body mass index, H , pylori infection, and fruit and salt intake, the adjusted odds ratio (OR) for GSTT1 and gastric cancer was 2.50 (95% confidence interval (CI), 1.01- 6.22). When gastric cancer cases were compared with CG patients, the adjust ed OR for GSTT1 was 2.33 (95% CI, 0.75-7.25). However, GSTT1 null genotype was not associated with the risk of CG when using population controls. No o bvious association was found between GSTM1 and the risk of both gastric can cer and CG, Our results suggest that GSTT1 null genotype may be associated with an increased risk of gastric cancer in a Chinese population.