GSTT1 and GSTM1 Deletions, NQO1 C609T Polymorphism and Risk of Chronic Myelogenous Leukemia in Japanese

Abstract

We conducted a prevalent case-control study with 51 chronic myelogenous leukemia (CML) cases and 476 controls ‍to investigate the associations between glutathione S-transferase T1 (GSTT1), glutathione S-transferase M1 (GSTM1) ‍deletions, and the NAD(P)H:quinone oxidoreductase 1 (NQO1) C609T polymorphism with risk of chronic myelocytic ‍leukemia in Japanese. For the GSTT1 deletion, when the GSTT1 positive genotype was defined as the reference, the ‍OR for the GSTT1 deletion genotype was 1.32 (95%CI; 0.74-2.36). For the GSTM1 deletion, when the GSTM1 ‍positive genotype was defined as the reference, the OR for the GSTM1 deletion genotype was 0.95 (95%CI; 0.53- ‍1.69). For NQO1 C609T polymorphism, when the NQO1 609CC genotype was defined as the reference, the ORs for ‍the CT genotype, TT genotype, and CT and TT genotypes combined together were 2.37 (95%CI, 1.21-4.67, P=0.012), ‍1.44 (0.55-3.74, P=0.012) and 2.12 (1.10-4.08, P=0.025), respectively. The present study revealed that the risk of CML ‍was modulated little by GSTT1 and GSTM1 deletions, but a statistically significant association between NQO1 C609T ‍polymorphism and CML was observed for Japanese. Incidence case-control studies with a larger statistical power ‍are now required to confirm our findings.