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Prognostic values of long non-coding RNA MIR22HG for patients with hepatocellular carcinoma after hepatectomy

机译:长非编码RNA MIR22HG对肝切除术后肝细胞癌患者的预后价值

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摘要

Hepatocellular carcinoma (HCC) is the fifth most frequently diagnosed cancer worldwide and the second most frequent cause of cancer death. The aim of this study is to identify the association between the expression of long non-coding RNA (lncRNA) MIR22HG and the clinical and tumor characteristics of patients with HCC, and to explore the prognostic significance of lncRNA MIR22HG on patients with HCC. We retrospectively reviewed 127 patients with HCC(42 female, 85 male) who were managed in our hospital between May 1st 2010 and June 30th 2016. The expressions of lncRNA MIR22HG were detected by real-time PCR. Prognostic factors were evaluated using Kaplan-Meier curves and Cox proportional hazards models. For the entire cohort of 127 patients, the normalized real-time PCR showed that the expression of lncRNA MIR22HG was lower in HCC tissues compared with corresponding nontumorous tissues. MTT assay showed that si-MIR22HG remarkably inhibited the proliferation tumor cells in three HCC cell lines including SMMC-7721, Huh-7 and Hep3B. Moreover, under-expression of MIR22HG was closely related to tumor encapsulation, microvascular invasion (MVI), and TNM stage. Cox proportional hazards analysis demonstrated that lncRNA MIR22HG under-expression was an independent risk factor associated with the prognosis of patients with HCC. In conclusion, we found that lncRNA MIR22HG expressed significantly lower in HCC tissues compared with non-tumorous tissues. Under-expression of lncRNAMIR22HG was an independent risk factor associated with the prognosis of patients with HCC.
机译:肝细胞癌(HCC)是全球第五大最常被诊断出的癌症,也是第二大最常导致癌症死亡的原因。这项研究的目的是确定长非编码RNA(lncRNA)MIR22HG的表达与肝癌患者的临床和肿瘤特征之间的关联,并探讨lncRNA MIR22HG对肝癌患者的预后意义。我们回顾性分析了2010年5月1日至2016年6月30日在我院接受治疗的127例HCC患者(女性42例,男性85例)。lncRNA MIR22HG的表达通过实时PCR检测。使用Kaplan-Meier曲线和Cox比例风险模型评估预后因素。对于127名患者的整个队列,归一化实时PCR显示,与相应的非肿瘤组织相比,HCC组织中lncRNA MIR22HG的表达更低。 MTT分析表明,si-MIR22HG显着抑制了包括SMMC-7721,Huh-7和Hep3B在内的三种HCC细胞系中的肿瘤细胞增殖。此外,MIR22HG的表达不足与肿瘤包囊,微血管浸润和TNM分期密切相关。 Cox比例风险分析表明,lncRNA MIR22HG表达不足是与HCC患者预后相关的独立危险因素。总之,我们发现与非肿瘤组织相比,lncRNA MIR22HG在HCC组织中表达明显降低。 lncRNAMIR22HG的表达不足是与HCC患者预后相关的独立危险因素。

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