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代谢酶CYP1A1、CYP2D6、GSTM1和GSTT1的基因多态性与白血病易感性

Genetic polymorphisms of metabolic enzymes CYP1A1, CYP2D6, GSTM1 and GSTT1 and leukemia susceptibility.

作者信息

Chen Han-Chun, Hu Wei-Xin, Liu Qing-Xia, Li Wen-Kai, Chen Fang-Zhi, Rao Zhou-Zhou, Liu Xin-Fa, Luo Ya-Ping, Cao Yan-Fei

机构信息

Department of Biochemistry, School of Biological Science and Technology, Central South University, Changsha, Hunan, China.

出版信息

Eur J Cancer Prev. 2008 Jun;17(3):251-8. doi: 10.1097/CEJ.0b013e3282b72093.

Abstract

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.

摘要

在中国湖南省长沙市汉族人群的204名健康人和348名白血病患者(包括急性淋巴细胞白血病(ALL)、急性非淋巴细胞白血病(ANLL)、慢性粒细胞白血病(CML))中,分析了生物转化I相酶细胞色素P450(CYP1A1和CYP2D6)和II相酶谷胱甘肽S-转移酶(GSTM1和GSTT1)的基因多态性。我们的结果显示,在急性淋巴细胞白血病、ANLL、慢性粒细胞白血病组和健康对照组中,CYP1A1、CYP2D6和GSTT1基因多态性的频率无显著差异。仅GSTM1基因缺失型的变异与ANLL的发生相关。在ANLL高危个体中发现了GSTM1基因缺失型与GSTT1基因缺失型的联合基因型,或GSTM1基因缺失型与CYP1A1杂合突变型的联合基因型,或GSTM1基因缺失型与CYP1A1杂合突变型和CYP2D6杂合突变型的联合基因型,或GSTM1基因缺失型与CYP1A1杂合突变型、CYP2D6杂合突变型和GSTT1基因缺失型的联合基因型。所有这些发现表明,单独的GSTM1基因缺失型或与其他代谢酶的相关基因型协同作用可能是ANLL病因学中的易感因素。

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