M. Hashemi, F. Bizhani, H. Danesh, B. Narouie, M. Sotoudeh, M. Radfar, M. Ramezani, G. Bahari, M. Taheri, S. Ghavami
{"title":"MiR-608 rs4919510 C > G polymorphism increased the risk of bladder cancer in an Iranian population","authors":"M. Hashemi, F. Bizhani, H. Danesh, B. Narouie, M. Sotoudeh, M. Radfar, M. Ramezani, G. Bahari, M. Taheri, S. Ghavami","doi":"10.3934/genet.2016.4.212","DOIUrl":null,"url":null,"abstract":"Abstract\n MicroRNAs (miRNAs) participate in diverse biological pathways and may act as oncogenes or tumor suppressors. The single nucleotide polymorphisms (SNPs) in miRNAs potentially can alter miRNA-binding sites on target genes as well as affecting miRNAs expression. The present study aimed to evaluate the impact of miR-608 rs4919510 C > G variant on bladder cancer risk. This case-control study conducted on 233 bladder cancer patients and 252 healthy subjects. Genotyping of miR-608 rs4919510 was done using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Our findings showed that CG as well as CG + GG genotypes significantly increased the risk of bladder cancer (OR = 1.94, 95% CI = 1.28–2.94, p = 0.002, and OR = 1.90, 95% CI = 1.26–2.86, p = 0.002, respectively) compared to CC genotype. The G allele significantly increased the risk of bladder cancer compared to C allele (OR = 1.69, 95% CI = 1.17–2.45, p = 0.005). Our findings proposed that miR-608 polymorphism might be associated with increased risk of bladder cancer in a sample of Iranian population. Further large-scale studies with different ethnicities are needed to verify our findings.","PeriodicalId":43477,"journal":{"name":"AIMS Genetics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2016-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIMS Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3934/genet.2016.4.212","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
Abstract
MicroRNAs (miRNAs) participate in diverse biological pathways and may act as oncogenes or tumor suppressors. The single nucleotide polymorphisms (SNPs) in miRNAs potentially can alter miRNA-binding sites on target genes as well as affecting miRNAs expression. The present study aimed to evaluate the impact of miR-608 rs4919510 C > G variant on bladder cancer risk. This case-control study conducted on 233 bladder cancer patients and 252 healthy subjects. Genotyping of miR-608 rs4919510 was done using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Our findings showed that CG as well as CG + GG genotypes significantly increased the risk of bladder cancer (OR = 1.94, 95% CI = 1.28–2.94, p = 0.002, and OR = 1.90, 95% CI = 1.26–2.86, p = 0.002, respectively) compared to CC genotype. The G allele significantly increased the risk of bladder cancer compared to C allele (OR = 1.69, 95% CI = 1.17–2.45, p = 0.005). Our findings proposed that miR-608 polymorphism might be associated with increased risk of bladder cancer in a sample of Iranian population. Further large-scale studies with different ethnicities are needed to verify our findings.
MicroRNAs (miRNAs)参与多种生物学途径,可能作为致癌基因或肿瘤抑制因子。mirna中的单核苷酸多态性(snp)可能改变靶基因上的mirna结合位点,并影响mirna的表达。本研究旨在评估miR-608 rs4919510 C > G变异对膀胱癌风险的影响。本研究对233例膀胱癌患者和252名健康受试者进行了病例对照研究。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对miR-608 rs4919510进行基因分型。我们的研究结果显示,与CC基因型相比,CG和CG + GG基因型显著增加膀胱癌的风险(OR = 1.94, 95% CI = 1.28-2.94, p = 0.002; OR = 1.90, 95% CI = 1.26-2.86, p = 0.002)。与C等位基因相比,G等位基因显著增加膀胱癌的风险(OR = 1.69, 95% CI = 1.17-2.45, p = 0.005)。我们的研究结果表明,miR-608多态性可能与伊朗人群样本中膀胱癌风险增加有关。需要对不同种族进行进一步的大规模研究来验证我们的发现。