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Association between donor and recipient smoothened gene polymorphisms and the risk of hepatocellular carcinoma recurrence following orthotopic liver transplantation in a Han Chinese population

机译:汉族人群原位肝移植后供体和受体平滑基因多态性与肝细胞癌复发风险之间的关联

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Hepatocellular carcinoma (HCC) recurrence after orthotopic liver transplantation (OLT) is potential cause for the poor outcome. Smoothened (SMO) gene has been considered associating with HCC and HCC recurrence, but its association with HCC recurrence after OLT is not clear yet. In this study, we aim at evaluating the association between donor and recipient SMO gene polymorphisms and HCC recurrence after OLT. A total of 76 patients with HCC who had undergone OLT from July 2007 to August 2012 were included. A single nucleotide polymorphism (SNP), SMO rs3824, located at the 3'UTR region, was genotyped and analyzed in both donor and recipient. We demonstrated that recipient rs3824 polymorphism was significantly associated with HCC recurrence following OLT. In multivariate logistic regression analysis, TNM stage (p = 0.001), recipient SMO rs3824 genotype (CG vs. CC/GG p = 0.001), and histologic grade (p = 0.019) were identified as independent risk factors of HCC recurrence. Recurrence-free survival (RFS) and overall survival (OS) were significantly higher in the recipient CC/GG group than in the CG group (p = 0.003 and p = 0.011, respectively). Cox proportional hazards modeling revealed that TNM stage, recipient SMO rs3824 genotype, pre-OLT serum AFP level, and histologic grade were independent factors (p < 0.05) for patients' clinical outcomes. In conclusion, recipient SMO rs3824 polymorphism is associated with an increased risk of HCC recurrence following OLT and has a potential clinical value for the prognosis of HCC patients treated with OLT.
机译:原位肝移植(OLT)后肝细胞癌(HCC)复发是不良预后的潜在原因。人们认为平滑化(SMO)基因与HCC和HCC复发相关,但尚不清楚它与OLT后HCC复发的相关性。在这项研究中,我们旨在评估供体和受体SMO基因多态性与OLT后HCC复发之间的关联。从2007年7月至2012年8月,共76例接受过OLT的HCC患者入选。对位于3'UTR区的单核苷酸多态性(SNP)SMO rs3824进行基因分型并在供体和受体中进行分析。我们证明了受体rs3824多态性与OLT后HCC复发显着相关。在多元逻辑回归分析中,TNM分期(p = 0.001),受者SMO rs3824基因型(CG vs. CC / GG p = 0.001)和组织学分级(p = 0.019)被确定为HCC复发的独立危险因素。接受CC / GG组的无复发生存期(RFS)和总生存期(OS)明显高于CG组(分别为p = 0.003和p = 0.011)。 Cox比例风险建模显示,TNM分期,受体SMO rs3824基因型,OLT前血清AFP水平和组织学分级是影响患者临床结局的独立因素(p <0.05)。总之,受体SMO rs3824多态性与OLT术后HCC复发的风险增加有关,对于用OLT治疗的HCC患者的预后具有潜在的临床价值。

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