首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Association of MDR1 Gene Polymorphisms with Susceptibilityto Hepatocellular Carcinoma in the Chinese PopulationAssociation of MDR1 GenePolymorphisms with Susceptibility to Hepatocellular Carcinoma in the Chinese Population
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Association of MDR1 Gene Polymorphisms with Susceptibilityto Hepatocellular Carcinoma in the Chinese PopulationAssociation of MDR1 GenePolymorphisms with Susceptibility to Hepatocellular Carcinoma in the Chinese Population

机译:中国人群中MDR1基因多态性与肝细胞癌易感性的关联中国人群中MDR1基因多态性与肝细胞癌易感性的关联

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Objective: The objective of this study was to evaluate the association of MDR1 gene polymorphisms withsusceptibility to hepatocellular carcinoma (HCC). Methods: A total of 689 HCC patients and 680 cancer-freesubjects were enrolled. Human MDR1 gene polymorphisms were investigated by created restriction sitepolymerasechain reaction (CRS-PCR) and DNA sequencing methods. Multiple logistic regression models wereapplied to estimate the association between MDR1 gene polymorphisms and susceptibility to HCC. Results:We detected a novel c.4125A>C polymorphism and our findings suggested that this variant was significantlyassociated with susceptibility to HCC. A significantly increased susceptibility to HCC was noted in the homozygotecomparison (CC versus AA: OR=1.621, 95% CI 1.143-2.300, χ2=7.4095, P=0.0065), recessive model (CC versusAC+AA: OR=1.625, 95% CI 1.167-2.264, χ2=8.3544, P=0.0039) and allele contrast (C versus A: OR=1.185, 95% CI1.011-1.389, χ2=4.4046, P=0.0358). However, no significant increase was observed in the heterozygote comparison(AC versus AA: OR=0.995, 95% CI 0.794-1.248, χ2=0.0017, P=0.9672) and dominant model (CC+AC versus AA:OR=1.106, 95% CI 0.894-1.369, χ2=0.8560, P=0.3549). Conclusions: These findings suggest that the c.4125A>Cpolymorphism of the MDR1 gene might contribute to susceptibility to HCC in the Chinese population. Furtherwork will be necessary to clarify the relationship between the c.4125A>C polymorphism and susceptibility toHCC on larger populations of diverse ethnicity.
机译:目的:本研究的目的是评估MDR1基因多态性与肝细胞癌(HCC)敏感性的关系。方法:总共招募了689例HCC患者和680例无癌受试者。人类MDR1基因多态性通过建立限制性酶切位点聚合酶链反应(CRS-PCR)和DNA测序方法进行了研究。应用多个逻辑回归模型估计MDR1基因多态性与肝癌易感性之间的关系。结果:我们检测到一种新的c.4125A> C多态性,我们的发现表明该变异与肝癌易感性显着相关。在纯合子比较中(CC vs AA:OR = 1.621,95%CI 1.143-2.300,χ2= 7.4095,P = 0.0065),隐性模型(CC vs AC + AA:OR = 1.625,95%),HCC敏感性显着增加。 CI 1.167-2.264,χ2= 8.3544,P = 0.0039)和等位基因对比(C对A:OR = 1.185,95%CI1.011-1.389,χ2= 4.4046,P = 0.0358)。然而,杂合子比较(AC与AA:OR = 0.995,95%CI 0.794-1.248,χ2= 0.0017,P = 0.9672)和显性模型(CC + AC与AA:OR = 1.106,95)均未观察到显着增加。 %CI 0.894-1.369,χ2= 0.8560,P = 0.3549)。结论:这些发现表明,MDR1基因的c.4125A> C多态性可能有助于中国人群对HCC的易感性。有必要做进一步的工作来阐明c.4125A> C多态性与不同种族的更多人群对HCC的易感性之间的关系。

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