GSTM1 and GSTT1 Polymorphisms and Susceptibility to Acute Myeloid Leukemia: A Case-control Study of the Sudanese Population

Ebtihal Ahmed Babekir, N. Abdelateif, Saadia Osman Adelrahim, R. Hassan, I. Ibrahim
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引用次数: 3

Abstract

Background: Glutathione S-transferase (GST) enzyme levels are associated with risk of many types of cancers, including hematological malignancies. In this study we here aimed to investigate the relationship between GSTM1 and GSTT1 polymorphisms and the risk of AML. Conflicts in the published results and the absence of similar in-depth studies in Sudan prompted us to perform the present case-control study to determine the frequency of GSTM1 and GSTT1 polymorphisms in AML patients and their possible association with AML in a Sudanese population.Materials and Methods: A total of 40 patients with AML and 40 control subjects were enrolled in this study. Blood samples were collected from all patients in EDTA containing tubes. Genomic DNA was extracted from all blood samples using salting out method. Genotyping for detection of GSTM1, and GSTT1 polymorphisms was performed for both patients and controls using a multiplex PCR. Results: We reported that there is an association between the GSTM1 null genotype and AML risk (OR= 2.7, 95% CI= 1.2-6.04; P.value = 0.012), the GSTT1 null genotype appeared also to have an influence in the development of AML (OR= 4.93, 95% CI= 1.6-15.07; P.value = 0.005).Conclusion: These findings indicate that genetic variants of GSTM1 and GSTT1 genes may increase individual susceptibility to AML.
GSTM1和GSTT1多态性与急性髓性白血病易感性:苏丹人群的病例对照研究
背景:谷胱甘肽s -转移酶(GST)酶水平与多种癌症的风险相关,包括血液系统恶性肿瘤。在这项研究中,我们旨在研究GSTM1和GSTT1多态性与AML风险之间的关系。已发表结果的冲突和苏丹缺乏类似的深入研究促使我们进行本病例对照研究,以确定AML患者中GSTM1和GSTT1多态性的频率及其与苏丹人群中AML的可能关联。材料与方法:本研究共纳入40例AML患者和40例对照组。所有患者的血样均在含有EDTA的试管中采集。采用盐析法提取所有血样的基因组DNA。采用多重PCR对患者和对照组进行基因分型,检测GSTM1和GSTT1多态性。结果:我们报道了GSTM1零基因型与AML风险之间存在关联(OR= 2.7, 95% CI= 1.2-6.04;p值= 0.012),GSTT1零基因型似乎也对AML的发展有影响(OR= 4.93, 95% CI= 1.6-15.07;p值= 0.005)。结论:这些发现提示GSTM1和GSTT1基因的遗传变异可能增加个体对AML的易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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