Hashemi Mohammad, Bahari Gholamreza, Sattarifard Hedieh, Narouie Behzad
Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan 98167-43181, Iran.
Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan 98167-43181, Iran.
Mol Clin Oncol. 2017 Oct;7(4):696-700. doi: 10.3892/mco.2017.1369. Epub 2017 Aug 8.
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.
本研究旨在检测前体微小RNA(miR)-3131的3个碱基对插入缺失(rs57408770)多态性对伊朗人群样本中前列腺癌(PCa)风险的影响。本病例对照研究共纳入340名受试者,包括177例PCa患者和170例良性前列腺增生患者。设计了错配聚合酶链反应-限制性片段长度多态性方法对3个碱基对插入缺失(rs57408770)多态性进行基因分型。本研究结果表明,该插入缺失变异在共显性模型中[比值比(OR)=2.23,95%置信区间(CI)=1.13 - 4.37;P = 0.021,插入(ins)/ins与缺失(del)/del相比]和隐性模型中(OR = 2.33,95% CI = 1.25 - 4.36;P = 0.009,ins/ins与del/del + del/ins相比)均显著增加PCa风险。总之,据我们所知,本研究结果首次提出miR-3131的3个碱基对插入缺失变异可能是伊朗人群样本中PCa易感性的一个风险因素。需要开展不同种族和更大样本量的进一步研究来验证本研究结果。