首页> 外文期刊>Cellular and molecular biology >The association between 1349T > G polymorphism of ApE1 gene and the risk of prostate cancer in northern Iran
【24h】

The association between 1349T > G polymorphism of ApE1 gene and the risk of prostate cancer in northern Iran

机译:伊朗北部ApE1基因1349T> G多态性与前列腺癌风险的关系

获取原文
获取原文并翻译 | 示例
           

摘要

Prostate cancer (PCa) is the most common malignancy in men and the fourth most common cause of death based on cancer all over the world. Many genes has been shown to be involved in the progress of the prostate cancer. Human apurinic/apyrimidinic endonuclease 1 (APE1) is a multifunctional protein that has an important role in the base excision repair (BER) pathway. The aim of this study was to evaluate the association of ApE1 1349T> G polymorphism and the susceptibility to prostate cancer in northern Iran population. Samples were collected from 100 patients diagnosed with prostate cancer patients and 100 controls subjects and genotyped by PCR-RFLP (Polymerase Chain Reaction-Restriction Fragment Length Polymorphism). We observed a significant difference in genotype distributions of ApE1 1349T> G polymorphism between patients and controls (P= 0.039). Our findings revealed individuals with the variant TG and GG had a significant increased risk of prostate cancer (GG: OR= 2.50, 95% CI= 1.063-5.874, P= 0.035. TG: OR= 2.40, 95% CI= 1.16-4.95, P= 0.017). Also, more analyses were showed that G allele were associated with increased risk of prostate cancer (OR= 1.493, 95% CI= 1.007-2.21, P= 0.045). The data from this study indicates that the ApE1 1349T> G polymorphism is associated with increased risk of prostate cancer. Although more studies should be considered with larger number of patients and control subjects to confirm our results.
机译:前列腺癌(PCa)是男性最常见的恶性肿瘤,也是全世界第四大最常见的死因。已显示许多基因参与前列腺癌的进展。人嘌呤/嘧啶核糖核酸内切酶1(APE1)是一种多功能蛋白,在碱基切除修复(BER)途径中具有重要作用。这项研究的目的是评估伊朗北部人群中ApE1 1349T> G多态性与对前列腺癌的敏感性之间的关系。从100名诊断为前列腺癌的患者和100名对照受试者中收集样本,并通过PCR-RFLP(聚合酶链反应-限制性片段长度多态性)进行基因分型。我们观察到患者和对照之间ApE1 1349T> G多态性的基因型分布存在显着差异(P = 0.039)。我们的发现显示,具有TG和GG变异的个体患前列腺癌的风险显着增加(GG:OR = 2.50,95%CI = 1.063-5.874,P = 0.035。TG:OR= 2.40,95%CI = 1.16-4.95 ,P = 0.017)。此外,更多的分析表明,G等位基因与前列腺癌的风险增加相关(OR = 1.493,95%CI = 1.007-2.21,P = 0.045)。该研究的数据表明,ApE1 1349T> G多态性与前列腺癌风险增加相关。尽管应考虑对更多的患者和对照组进行更多的研究,以证实我们的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号