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首页> 外文期刊>Toxicological Sciences >Joint Effects of XRCC1 Polymorphisms and Polycyclic Aromatic Hydrocarbons Exposure on Sperm DNA Damage and Male Infertility
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Joint Effects of XRCC1 Polymorphisms and Polycyclic Aromatic Hydrocarbons Exposure on Sperm DNA Damage and Male Infertility

机译:XRCC1基因多态性和多环芳烃暴露对精子DNA损伤和男性不育的联合影响

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摘要

X-ray repair cross-complementing group 1 (XRCC1) plays a role in repairing polycyclic aromatic hydrocarbons (PAHs)-induced DNA damage. We examined the effects of exposure to PAHs and XRCC1 polymorphism, alone or combined, on sperm DNA integrity and male fertility. A total of 620 idiopathic infertile subjects and 273 fertile controls were recruited in this study. PAHs exposure was indicated by urinary 1-hydroxypyrene level. Genotypes were determined by PCR-RFLP, and sperm DNA damage was detected by Tdt-mediated dUTP nick end labelling assay using flow cytometry. A positive correlation was found between PAHs exposure and sperm DNA damage (beta coefficients = 0.183, p 0.001), whereas there was no significant association between the XRCC1 polymorphisms and sperm DNA damage. However, when the patients were dichotomized for PAHs exposure, higher sperm DNA damage was found among 399Gln allele carriers compared with the wild-type homozygotes (p = 0.033). Further analysis based on a case-control study revealed the joint effect of XRCC1-399 polymorphism and PAHs exposure on the risk of male infertility (p interaction = 0.041). These findings provided the first evidence about potential joint effects of PAHs exposure and DNA repair gene polymorphisms on male reproductive system and may be helpful in improving our understanding of the etiology of male infertility.
机译:X射线修复交叉互补基团1(XRCC1)在修复多环芳烃(PAHs)诱导的DNA损伤中发挥作用。我们检查了单独或联合暴露于PAHs和XRCC1多态性对精子DNA完整性和雄性育性的影响。这项研究共招募了620名特发性不育受试者和273名可育对照。 PAHs暴露是通过尿中的1-羟基level水平指示的。通过PCR-RFLP确定基因型,并使用流式细胞术通过Tdt介导的dUTP缺口末端标记测定法检测精子DNA损伤。在PAHs暴露与精子DNA损伤之间发现正相关(β系数= 0.183,p <0.001),而XRCC1多态性与精子DNA损伤之间没有显着关联。但是,将患者按PAHs暴露二分法时,与野生型纯合子相比,在399Gln等位基因携带者中发现了更高的精子DNA损伤(p = 0.033)。基于病例对照研究的进一步分析揭示了XRCC1-399多态性和PAHs暴露对男性不育风险的联合影响(p相互作用= 0.041)。这些发现为PAHs暴露和DNA修复基因多态性对男性生殖系统的潜在联合作用提供了第一个证据,可能有助于增进我们对男性不育病因的理解。

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