Bănescu Claudia, Iancu Mihaela, Trifa Adrian P, Cândea Marcela, Benedek Lazar Erzsebet, Moldovan Valeriu G, Duicu Carmen, Tripon Florin, Crauciuc Andrei, Dobreanu Minodora
Department of Medical Genetics, University of Medicine and Pharmacy Targu Mures, 38 Gh Marinescu Street, 540139 Targu Mures, Romania.
Department of Medical Informatics and Biostatistics, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, 8 Victor Babes Street, 400012 Cluj-Napoca, Romania.
Oxid Med Cell Longev. 2016;2016:2536705. doi: 10.1155/2016/2536705. Epub 2015 Dec 28.
Oxidative stress might contribute to the occurrence of cancers, including the hematological ones. Various genetic polymorphisms were shown to increase the quantity of reactive oxygen species, a phenomenon that is able to induce mutations and thus promote cancers. The purpose of the study was to evaluate the association between CAT C262T, GPX1 Pro198Leu, MnSOD Ala16Val, GSTM1, GSTT1, and GSTP1 Ile105Val gene polymorphisms and acute myeloid leukemia risk, in a case-control study comprising 102 patients and 303 controls. No association was observed between AML and variant genotypes of CAT, MnSOD, GSTM1, and GSTT1 polymorphisms. Our data revealed a statistically significant difference regarding the frequencies of GPX1 Pro198Leu and GSTP1 Ile105Val variant genotypes between AML patients and controls (p < 0.001). Our results showed no association in the distribution of any of the CAT C262T, GPX1 Pro198Leu, GSTM1, GSTT1, and GSTP1 polymorphisms regarding age, gender, FAB subtype, cytogenetic risk groups, FLT3 and DNMT3 gene mutations, and overall survival. Our data suggests that the presence of variant allele and genotype of GPX1 Pro198Leu and GSTP1 Ile105Val gene polymorphisms may modulate the risk of developing AML.
氧化应激可能促使包括血液系统癌症在内的多种癌症发生。多种基因多态性被证实可增加活性氧的数量,这一现象能够诱发突变从而促进癌症发展。本研究旨在通过一项包含102例患者和303例对照的病例对照研究,评估CAT C262T、GPX1 Pro198Leu、MnSOD Ala16Val、GSTM1、GSTT1和GSTP1 Ile105Val基因多态性与急性髓系白血病风险之间的关联。未观察到急性髓系白血病与CAT、MnSOD、GSTM1和GSTT1多态性的变异基因型之间存在关联。我们的数据显示,急性髓系白血病患者与对照之间,GPX1 Pro198Leu和GSTP1 Ile105Val变异基因型的频率存在统计学显著差异(p < 0.001)。我们的结果表明,在年龄、性别、FAB亚型、细胞遗传学风险组、FLT3和DNMT3基因突变以及总生存方面,CAT C262T、GPX1 Pro198Leu、GSTM1、GSTT1和GSTP1多态性的任何一种分布均无关联。我们的数据表明,GPX1 Pro198Leu和GSTP1 Ile105Val基因多态性的变异等位基因和基因型的存在可能会调节患急性髓系白血病的风险。