首页> 美国卫生研究院文献>Oncotarget >Variations within 3′-UTR of MDM4 gene contribute to clinical outcomes of advanced non-small cell lung cancer patients following platinum-based chemotherapy
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Variations within 3′-UTR of MDM4 gene contribute to clinical outcomes of advanced non-small cell lung cancer patients following platinum-based chemotherapy

机译:铂类化疗后MDM4基因3-UTR内的变异有助于晚期非小细胞肺癌患者的临床结局

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摘要

Single-nucleotide polymorphism (SNPs) in microRNA (miRNA)-binding sites may modulate the posttranscriptional regulation of gene expression and explain individual sensitivity to platinum agents. This study aimed to investigate the impact of SNPs located at 3′-untranslated region (UTR) of MDM4 gene, on clinical outcomes of advanced non-small cell lung cancer (NSCLC) patients. Four SNPs were genotyped by using DNA from blood samples of advanced NSCLC patients (642 in the Discovery set and 330 in the Replication set) and were analyzed the relationships with clinical outcomes. Carriers with rs10900598 CC genotype and rs4245739 AC genotype showed increased overall survival (OS) than those with AA genotype (P = 0.017 and P = 0.037, respectively) in the Discovery set and after pooling results from the Replication set. A combined effect on survival of variant alleles was also concluded and validated. Stratification analysis revealed that the effect of MDM4 SNPs was more pronounced in lung adenocarcinoma (LAC) subgroups. A reduced expression of the reporter gene for the C allele of rs4245739 was observed in NSCLC cells using luciferase reporter gene assays. Taken together, our results demonstrate that genetic variations in 3′-UTR of MDM4 gene may influence outcomes of advanced NSCLC by miRNAs-mediated regulation.
机译:microRNA(miRNA)结合位点中的单核苷酸多态性(SNP)可能会调节基因表达的转录后调控,并解释个体对铂试剂的敏感性。这项研究旨在调查位于MDM4基因3'-非翻译区(UTR)的SNP对晚期非小细胞肺癌(NSCLC)患者临床结局的影响。使用晚期NSCLC患者血液样本中的DNA(发现组中的642个,复制组中的330个)对四个SNP进行基因分型,并分析其与临床结局的关系。在发现组中以及从复制组合并结果后,具有rs10900598 CC基因型和rs4245739 AC基因型的载体显示的总体生存期(OS)比具有AA基因型的载体(分别为P = 0.017和P = 0.037)高。还总结并验证了对变异等位基因存活的综合影响。分层分析显示,MDM4 SNP在肺腺癌(LAC)亚组中的作用更为明显。使用萤光素酶报告基因检测,在NSCLC细胞中观察到rs4245739 C等位基因报告基因的表达降低。两者合计,我们的结果表明,MDM4基因3'-UTR的遗传变异可能通过miRNA介导的调控影响晚期NSCLC的预后。

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