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首页> 外文期刊>European journal of cancer prevention: The official journal of the European Cancer Prevention Organisation (ECP) >Genetic polymorphisms of metabolic enzymes CYP1A1, CYP2D6, GSTM1 and GSTT1 and leukemia susceptibility.
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Genetic polymorphisms of metabolic enzymes CYP1A1, CYP2D6, GSTM1 and GSTT1 and leukemia susceptibility.

机译:代谢酶CYP1A1,CYP2D6,GSTM1和GSTT1的遗传多态性与白血病易感性。

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摘要

The genetic polymorphisms of biotransformation phase I enzymes, cytochrome P450 (CYP1A1 and CYP2D6), and phase II enzymes, glutathione S-transferase (GSTM1 and GSTT1), were analyzed in 204 healthy persons and 348 leukemia patients, who suffered from also acute lymphoblastic leukemia (ALL), acute nonlymphoblastic leukemia (ANLL) chronic myelogenous leukemia (CML), from the Han ethnic group in Changsha City of Hunan Province of China. Our results showed that the frequencies of polymorphisms of CYP1A1, CYP2D6 and GSTT1 among the groups including acute lymphoblastic leukemia, ANLL, chronic myelogenous leukemia and healthy control have no significant differences. The variation of GSTM1-null genotype alone correlated with the development of ANLL. The combined genotypes of GSTM1-null with GSTT1-null, or GSTM1-null with CYP1A1 heterozygous mutant, or GSTM1-null with CYP1A1 heterozygous mutant and CYP2D6 heterozygous mutant, or GSTM1-null with CYP1A1 heterozygous mutant, CYP2D6 heterozygous mutant and GSTT1-null were found in individuals with high risk of ANLL. All these findings suggest that GSTM1-null genotype alone or in coordination with the relevant genotypes of other metabolic enzymes might be susceptibility factors in the etiology of ANLL.
机译:在204名健康人和348名患有急性淋巴细胞白血病的患者中分析了生物转化I期酶细胞色素P450(CYP1A1和CYP2D6)和II期酶谷胱甘肽S-转移酶(GSTM1和GSTT1)的遗传多态性。 (ALL),来自中国湖南省长沙市汉族的急性非淋巴细胞性白血病(ANLL)慢性粒细胞性白血病(CML)。我们的研究结果表明,CYP1A1,CYP2D6和GSTT1基因多态性的频率在急性淋巴细胞白血病,ANLL,慢性粒细胞性白血病和健康对照人群之间没有显着差异。单独的GSTM1无效基因型的变异与ANLL的发展有关。 GSTM1-null与GSTT1-null或GSTM1-null与CYP1A1杂合突变体,GSTM1-null与CYP1A1杂合突变体和CYP2D6杂合突变体或GSTM1-null与CYP1A1杂合突变体,CYP2Dn被发现在ANLL高危人群中。所有这些发现表明,单独或与其他代谢酶的相关基因型配合使用的GSTM1空基因型可能是ANLL病因的易感性因素。

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