首页> 外文期刊>Leukemia and lymphoma >Polymorphisms of glutathione S-transferase Mu 1, glutathione S-transferase theta 1 and glutathione S-transferase Pi 1 genes in Hodgkin's lymphoma susceptibility and progression.
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Polymorphisms of glutathione S-transferase Mu 1, glutathione S-transferase theta 1 and glutathione S-transferase Pi 1 genes in Hodgkin's lymphoma susceptibility and progression.

机译:霍奇金淋巴瘤易感性和发展过程中谷胱甘肽S-转移酶Mu 1,谷胱甘肽S-转移酶θ1和谷胱甘肽S-转移酶Pi 1基因的多态性。

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摘要

We tested in this study whether the polymorphisms of the glutathione S-transferase Mu1 (GSTM1), glutathione S-transferase Theta 1 (GSTT1) and glutathione S-transferase Pi 1 (GSTP1), involved in metabolism of chemical agents, cell proliferation and cell survival, alter the risk for Hodgkin lymphoma (HL). Genomic DNA from 110 consecutive patients with HL and 226 controls was analysed by polymerase chain reaction and restriction digestion for the polymorphism analyses. Similar frequencies of the GSTM1 and GSTT1 genotypes were seen in patients and controls. In contrast, the frequency of the GSTP1 wild genotype (59.1%versus 36.3%, P = 0.004) was higher in patients than in controls. Individuals with the wild genotype had a 2.68 (95%CI: 1.38-5.21)-fold increased risk for the disease than others. An excess of the GSTP1 wild genotype was also observed in patients with tumors of stages III + IV when compared with those with tumors of stages I + II (39.1%versus 20.0%, P = 0.03). These results suggest that the wild allele of the GSTP1 gene is linked to an increased risk and high aggressiveness of the HL in our cases but they should be confirmed by further studies with larger cohorts of patients and controls.
机译:我们在这项研究中测试了谷胱甘肽S-转移酶Mu1(GSTM1),谷胱甘肽S-转移酶Theta 1(GSTT1)和谷胱甘肽S-转移酶Pi 1(GSTP1)的多态性是否参与化学物质的代谢,细胞增殖和细胞生存,改变霍奇金淋巴瘤(HL)的风险。通过聚合酶链反应和限制性消化分析110例连续HL患者和226例对照的基因组DNA,进行多态性分析。在患者和对照中发现了GSTM1和GSTT1基因型的相似频率。相比之下,患者中GSTP1野生基因型的频率(59.1%比36.3%,P = 0.004)高于对照组。具有野生基因型的个体罹患该疾病的风险比其他人增加了2.68倍(95%CI:1.38-5.21)。与患有I + II期肿瘤的患者相比,在III + IV期肿瘤的患者中也观察到了过量的GSTP1野生基因型(39.1%对20.0%,P = 0.03)。这些结果表明,在我们的病例中,GSTP1基因的野生等位基因与HL的风险增加和高侵袭性有关,但应通过对更大范围的患者和对照组进行进一步研究来证实。

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