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锰超氧化物歧化酶和谷胱甘肽过氧化物酶1单基因多态性与前列腺癌及血清前列腺特异性抗原水平相关性的一项初步研究。

A pilot study of the association of manganese superoxide dismutase and glutathione peroxidase 1 single gene polymorphisms with prostate cancer and serum prostate specific antigen levels.

作者信息

Parlaktas Bekir Suha, Atilgan Dogan, Gencten Yusuf, Benli Ismail, Ozyurt Huseyin, Uluocak Nihat, Erdemir Fikret

机构信息

Department of Urology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey.

Department of Biochemistry, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey.

出版信息

Arch Med Sci. 2015 Oct 12;11(5):994-1000. doi: 10.5114/aoms.2015.54853.

Abstract

INTRODUCTION

The aim of the study was to evaluate the potential association of single gene polymorphisms of the antioxidant enzymes manganese superoxide dismutase (MnSOD) and glutathione peroxidase (GPX1) with prostate cancer (PCa).

MATERIAL AND METHODS

Manganese superoxide dismutase and glutathione peroxidase 1 genotypes and allele frequencies in 49 prostate cancer cases (PCa group) and 98 control subjects were determined. Analysis of genotypes in control group individuals were performed in two subgroups according to serum prostate-specific antigen levels: the control group (n = 49), with prostate specific antigen (PSA) level < 4 ng/ml; and the nonPCa-high PSA control group (n = 49), with serum PSA > 4 ng/ml. Determination of MnSOD Ala-9Val and GPX1 Pro198Leu polymorphisms was performed using real-time polymerase chain reaction amplification.

RESULTS

No association was found between GPX1 polymorphisms and PCa in all groups (p > 0.05). In the PCa group, the frequency of homozygote Val allele carriers was significantly higher in comparison to nonPCa-high PSA control cases. Therefore, Val/Val genotype was found significantly suspicious for PCa risk (OR = 2.48; 95% CI: 1.37-4.48; p = 0.002). Furthermore, an overall protective effect of the Ala allele of the MnSOD polymorphism on PCa risk was detected. These findings in this small Turkish population suggested that individual risk of PCa may be modulated by MnSOD polymorphism especially in patients with high PSA, but GPX1 polymorphism seemed to have no effect on PCa risk.

CONCLUSIONS

The presence of genetic variants of antioxidant enzymes could have a potential influence on genesis of prostatic malignancy.

摘要

引言

本研究旨在评估抗氧化酶锰超氧化物歧化酶(MnSOD)和谷胱甘肽过氧化物酶(GPX1)的单基因多态性与前列腺癌(PCa)之间的潜在关联。

材料与方法

测定了49例前列腺癌患者(PCa组)和98例对照者中锰超氧化物歧化酶和谷胱甘肽过氧化物酶1的基因型及等位基因频率。根据血清前列腺特异性抗原水平,将对照组个体的基因型分析分为两个亚组:对照组(n = 49),前列腺特异性抗原(PSA)水平<4 ng/ml;非PCa高PSA对照组(n = 49),血清PSA>4 ng/ml。采用实时聚合酶链反应扩增法测定MnSOD Ala-9Val和GPX1 Pro198Leu多态性。

结果

在所有组中均未发现GPX1多态性与PCa之间存在关联(p>0.05)。在PCa组中,纯合子Val等位基因携带者的频率显著高于非PCa高PSA对照病例。因此,发现Val/Val基因型对PCa风险具有显著可疑性(OR = 2.48;95%CI:1.37 - 4.48;p = 0.002)。此外,检测到MnSOD多态性的Ala等位基因对PCa风险具有总体保护作用。在这个小的土耳其人群中的这些发现表明,PCa的个体风险可能受MnSOD多态性调节,尤其是在PSA高的患者中,但GPX1多态性似乎对PCa风险没有影响。

结论

抗氧化酶基因变异的存在可能对前列腺恶性肿瘤的发生有潜在影响。

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Glutathione peroxidases as oncotargets.谷胱甘肽过氧化物酶作为肿瘤靶点。
Oncotarget. 2017 Aug 16;8(45):80093-80102. doi: 10.18632/oncotarget.20278. eCollection 2017 Oct 3.

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