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Gene Polymorphism of Xenobiotic Biotransformation Enzymes in Patients with Classical Ph-Negative Myeloproliferative Neoplasms

机译:古典pH阴性髓原肿瘤患者异黄生物转化酶的基因多态性

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摘要

The correlation of gene polymorphisms rs4025935 (large deletion), rs1695 (313A>G), rs71748309 (large deletion), and rs1800566 (609C>T) of GSTM1, GSTT1, and NQO1 genes encoding glutathione-S-transferases (GST) M1, P1, and T1 and NADPH-quinone oxidoreductase with the risk of development of classical Ph-negative myeloproliferative neoplasms (polycythemia vera, essential thrombocythemia, and primary myelofibrosis) was studied in the Caucasian ethnicity population of Vyatka region of the Russian Federation. It was found that NQO1*609T allele, NQO1*609T genotypes, and homozygous carriage of a deletion (null) allele of GSTT1 gene are associated with the risk of development of myeloproliferative neoplasms (OR=1.29, 95%CI=1.02-1.64, p=0.04; OR=1.39, 95%CI=1.04-1.85, p=0.03; and OR=1.48, 95%CI=1.03-2.12, p=0.03, respectively). However, no influence of GSTM1 and GSTP1 gene polymorphisms on the risk of development of myeloproliferative disorders was registered.
机译:基因多态性RS4025935(大缺失),RS1695(313A> G),RS71748309(大缺失)和GSTM1,GSTT1和NQO1基因的RS1800566(609C> T)的相关性,所述GSTM1,GSTT1和NQO1基因编码(GST)M1, 在俄罗斯联邦的Vyatka地区的白种人种群中,研究了具有古典pH阴性肌酚瘤的风险(多胆血症Vera,基本血小伤症和原发性骨髓纤维化)的风险的P1和NADPH-醌氧化还原酶。 发现NQO1 * 609T等位基因,NQO1 * 609T基因型和GSTT1基因的缺失等位基因的纯合的载体与Myeloproiferative肿瘤的发育风险有关(或= 1.29,95%CI = 1.02-1.64, P = 0.04;或= 1.39,95%CI = 1.04-1.85,P = 0.03;和= 1.48,95%CI = 1.03-2.12,P = 0.03)。 然而,没有对Mencoproiferative障碍发育风险的GSTM1和GSTP1基因多态性的影响是未注册的。

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