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Interaction analysis of miR-1275/IGF2BP1/IGF2BP3 with the susceptibility to hepatocellular carcinoma

机译:miR-1275 / IGF2BP1 / IGF2BP3与肝细胞癌敏感性的相互作用分析

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摘要

Aim: The aim of this study was to investigate the association of miR-1275 rs16759, IGF2BP1 rs11079850 and IGF2BP3 rs34414305 with hepatocellular carcinoma (HCC) risk. Materialsandmethods: Genotyping of the rs16759 and rs11079850 was performed using a Taqman assay and genotyping of the rs34414305 was performed using PCR. Relative expression of miR-1275, IGF2BP1 and IGF2BP3 was examined using quantitative PCR. Results: Comparison of the rs16759GG, CG/GG and CC genotype showed an increased risk of HCC. When comparing G with C allele, a significantly increased risk of HCC was also found. The rs16759, rs11079850 and rs34414305 had combined the interactive effects on the carcinogenesis of HCC. Moreover, the rs34414305 Del/ATT-Del/Del carriers displayed lower levels of IGF2BP3. Conclusion: The rs16759, rs11079850 and rs34414305 may singly and interactively contribute to carcinogenesis of HCC.
机译:目的:本研究的目的是调查MIR-1275 RS16759,IGF2BP1 RS11079850和IGF2BP3 RS34414305的肝细胞癌(HCC)风险的关联。 MaterserAddMethods:使用Taqman测定进行RS16759和RS11079850的基因分型,使用PCR进行RS34414305的基因分型。 使用定量PCR检查miR-1275,IGF2BP1和IGF2BP3的相对表达。 结果:RS16759GG,CG / GG和CC基因型的比较显示出HCC的风险增加。 在用C等位基因比较G时,还发现了HCC的显着增加。 RS16759,RS11079850和RS34414305综合了对HCC致癌作用的互动影响。 此外,RS34414305 Del / Att-Del / Del载波显示了较低的IGF2BP3。 结论:RS16759,RS11079850和RS34414305可以单独和互动地促进HCC的致癌作用。

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