M. Hashemi, F. Bizhani, H. Danesh, B. Narouie, M. Sotoudeh, M. Radfar, M. Ramezani, G. Bahari, M. Taheri, S. Ghavami
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引用次数: 7
摘要
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。
MiR-608 rs4919510 C > G polymorphism increased the risk of bladder cancer in an Iranian population
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.