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Expression of microRNA-122 and microRNA-22 in HBV-related liver cancer and the correlation with clinical features

机译:MicroRNA-122和MicroRNA-22在HBV相关肝癌中的表达及与临床特征的相关性

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OBJECTIVE: MicroRNAs (miR) participate in cell proliferation, apoptosis and transformation, as they can regulate gene expression and intracellular signal transduction for various physiological processes. MiR-122 and miR-22 are known to be related with occurrence and progression of hepatitis B virus (HBV)-related hepatocellular cancer (HCC). This study recruited HBV-related HCC patients, whose expression levels of miR-122 and miR-22 were determined to analyze the correlation with clinical and pathological indexes. PATIENTS AND METHODS: HBV-related HCC patients were enrolled, in parallel with patients suffering from benign liver disease and non-HBV-related HCC. Real-time PCR was employed to measure miR-122 and miR-22 expression levels. RESULTS: The relative expression levels of miR-122 and miR-22 in HBV-related HCC patients were 1.26 ± 2.73 and 5.49 ± 3.91, respectively, which were significantly lower than that in benign liver disease or non-HBV-related HCC patients (p 0.05). The miR-122 and miR-22 levels were negatively correlated with tumor size, lymph node metastasis, TNM stage, pathological type, differentiation grade, liver cirrhosis, AFP and HBV DNA, all of which were independent risk factors (p < 0.05). CONCLUSIONS: MiR-122 and miR-22 were downregulated in HBV-related HCC patients, and were related with tumor size, lymph node metastasis, TNM stage, pathological type, differentiation grade, liver cirrhosis, AFP and HBV DNA.
机译:目的:Micrornas(MIR)参与细胞增殖,细胞凋亡和转化,因为它们可以调节各种生理过程的基因表达和细胞内信号转导。已知miR-122和miR-22与乙型肝炎病毒(HBV)的肝细胞癌(HCC)的发生和进展有关。本研究招募了HBV相关的HCC患者,其表达水平的miR-122和miR-22的表达水平分析与临床和病理指标的相关性。患者及方法:与患有良性肝病和非HBV相关的HCC的患者并行注册了HBV相关的HCC患者。使用实时PCR测量miR-122和miR-22表达水平。结果:HBV相关的HCC患者MIR-122和MIR-22的相对表达水平分别为1.26±2.73和5.49±3.91,其显着低于良性肝病或非HBV相关的HCC患者( P 0.05)。 MiR-122和MiR-22水平与肿瘤大小,淋巴结转移,TNM阶段,病理型,分化等级,肝硬化,AFP和HBV DNA负相关,所有这些都是独立的危险因素(P <0.05)。结论:MIR-122和MIR-22在HBV相关的HCC患者中下调,与肿瘤大小,淋巴结转移,TNM阶段,病理型,分化等级,肝硬化,AFP和HBV DNA有关。

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