首页> 美国卫生研究院文献>Molecular and Clinical Oncology >Evaluation of a 3-base pair indel polymorphism within pre-microRNA-3131 in patients with prostate cancer using mismatch polymerase chain reaction-restriction fragment length polymorphism
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Evaluation of a 3-base pair indel polymorphism within pre-microRNA-3131 in patients with prostate cancer using mismatch polymerase chain reaction-restriction fragment length polymorphism

机译:使用错配聚合酶链反应-限制性片段长度多态性评估前列腺癌患者pre-microRNA-3131中3碱基对插入/缺失多态性

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摘要

The present study aimed to examine the impact of a 3-bp indel (rs57408770) polymorphism within the pre-microRNA (miR)-3131 polymorphism on prostate cancer (PCa) risk in a sample of an Iranian population. In total, 340 subjects, including 177 patients with PCa and 170 patients with benign prostatic hyperplasia, were enrolled in the present case-control study. A mismatch polymerase chain reaction-restriction fragment length polymorphism method was designed for genotyping the 3-bp indel (rs57408770) polymorphism. The present findings demonstrated that the indel variant significantly increased the risk of PCa in codominant [odds ratio (OR)=2.23, 95% confidence interval (CI)=1.13–4.37; P=0.021, insertion (ins)/ins vs. deletion (del)/del] and recessive (OR=2.33, 95% CI=1.25–4.36; P=0.009, ins/ins vs. del/del + del/ins). In conclusion, to the best of our knowledge, the present findings for the first time proposed that a 3-bp indel variant of miR-3131 may be a risk factor for susceptibility to PCa in a sample of an Iranian population. Further studies with different ethnicities and larger sample sizes are required to validate the present findings.
机译:本研究旨在检查伊朗人群样本中pre-microRNA(miR)-3131多态性内3 bp indel(rs57408770)多态性对前列腺癌(PCa)风险的影响。本病例对照研究共招募了340名受试者,其中包括177名PCa患者和170名前列腺增生患者。设计了错配聚合酶链反应-限制性片段长度多态性方法,用于对3-bp indel(rs57408770)多态性进行基因分型。目前的发现表明,插入缺失变异体显着增加了PCa风险[优势比(OR)= 2.23,95%置信区间(CI)= 1.13-4.37; P = 0.021,插入(ins)/ ins与删除(del)/ del]和隐性(OR = 2.33,95%CI = 1.25-4.36; P = 0.009,ins / ins与del / del + del / ins )。总之,据我们所知,本研究结果首次提出,miR-3131的3 bp indel变异体可能是伊朗人群样本中PCa易感性的危险因素。需要进一步的研究,以不同的种族和更大的样本量来验证目前的发现。

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