Kang Seong-Ho, Kim Tae Young, Kim Ho Young, Yoon Jong-Hyun, Cho Han-Ik, Yoon Sung Soo, Kang Dae Hee, Suh Cheol Won, Lee Jae Hoon, Lee Dong Soon
Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Acta Haematol. 2008;119(1):60-4. doi: 10.1159/000117572. Epub 2008 Feb 20.
We had previously reported the association of the NQO1*2/2 polymorphism with a decreased risk for multiple myeloma (MM) in Koreans (odds ratio, OR, 0.24; 95% confidence interval, CI, 0.01-0.68). The associations of polymorphisms of other metabolizing enzymes (CYP1A1, GSTM1 and GSTT1) with the MM risk were investigated in 116 Korean MM patients and 176 Korean controls using TaqMan allelic discrimination and multiplex polymerase chain reaction. The ORs for CYP1A11/2A and CYP1A11/2B genotypes were 0.43 (95% CI, 0.19-0.98) and 0.51 (95% CI, 0.26-0.98), respectively, which was significantly associated with a decreased MM risk. With regard to CYP1A1 alleles, the OR for the CYP1A12A allele was 0.57 (95% CI, 0.326-0.995), which was also significantly associated with a decreased MM risk. However, null types of GSTM1 and GSTT1 polymorphisms were not associated with the MM risk. These results were different from those of a previous report on Caucasians which suggested the association of the GSTT1 polymorphism with an increased MM risk and no association of CYP1A1 with the MM risk. The associations of polymorphisms of metabolizing enzymes with the risk for MM differed between Koreans and Caucasians, suggesting an ethnic variation in the susceptibility to MM.
我们之前曾报道,在韩国人中,NQO1*2/2多态性与多发性骨髓瘤(MM)风险降低相关(优势比,OR,0.24;95%置信区间,CI,0.01 - 0.68)。我们使用TaqMan等位基因鉴别和多重聚合酶链反应,在116例韩国MM患者和176例韩国对照中,研究了其他代谢酶(CYP1A1、GSTM1和GSTT1)的多态性与MM风险的关联。CYP1A11/2A和CYP1A11/2B基因型的OR分别为0.43(95%CI,0.19 - 0.98)和0.51(95%CI,0.26 - 0.98),这与MM风险降低显著相关。关于CYP1A1等位基因,CYP1A12A等位基因的OR为0.57(95%CI,0.326 - 0.995),这也与MM风险降低显著相关。然而,GSTM1和GSTT1多态性的无效类型与MM风险无关。这些结果与之前关于高加索人的报告不同,之前的报告表明GSTT1多态性与MM风险增加相关,而CYP1A1与MM风险无关。韩国人和高加索人之间,代谢酶多态性与MM风险的关联不同,这表明在MM易感性方面存在种族差异。