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生物信息学分析鉴定用于预测肝细胞癌转移的多信使 RNA 标志物。

Bioinformatic Analysis to Identify a Multi-mRNA Signature for the Prediction of Metastasis in Hepatocellular Carcinoma.

机构信息

Institute of Hepatology, The Third People's Hospital of Changzhou, Jiangsu, P.R. China.

Department of Tumor Interventional Oncology, Renji South Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, P.R. China.

出版信息

DNA Cell Biol. 2020 Nov;39(11):2028-2039. doi: 10.1089/dna.2020.5513. Epub 2020 Sep 10.

Abstract

Hepatocellular carcinoma (HCC) with metastasis indicates worse prognosis for patients. However, the current methods are insufficient to accurately predict HCC metastasis at early stage. Based on the expression profiles of three Gene Expression Omnibus datasets, the differentially expressed genes associated with HCC metastasis were screened by online analytical tool GEO2R and weighted gene co-expression network analysis. Second, a risk score model including 27-mRNA was established by univariate Cox regression analyses, time-dependent ROC curves and least absolute shrinkage and selection operator Cox regression analysis. Then, we validated the model in cohort The Cancer Genome Atlas-liver hepatocellular carcinoma and analyzed the functions and key signaling pathways of the genes associated with the risk score model. According to the risk score model, patients were divided into two subgroups (high risk and low risk groups). The metastasis rate between two subgroups was significantly different in training cohort ( < 0.0001, hazard ratio [HR]: 10.3, confidence interval [95% CI]: 6.827-15.55) and external validation cohort ( = 0.0008, HR: 1.768, 95% CI: 1.267-2.467). Multivariable analysis showed that the risk score model was superior to and independent of other clinical factors (such as tumor stage, tumor size, and other parameters) in predicting early HCC metastasis. Moreover, the risk score model could predict the overall survival of patients with HCC. Finally, most of 27-mRNA were enriched in exosome and membrane bounded organelle, and these were involved in transportation and metabolic biological process. Protein-protein interaction network analysis showed most of these genes might be key genes affecting the progression of HCC. In addition, 3 genes of 27-mRNA were also differentially expressed in peripheral blood mononuclear cell. In conclusion, by using two combined methods and a broader of HCC datasets, our study provided reliable and superior predictive model for HCC metastases, which will facilitate individual medical management for these high metastatic risk HCC patients.

摘要

肝细胞癌(HCC)转移表明患者预后更差。然而,目前的方法不足以在早期准确预测 HCC 转移。基于三个基因表达谱数据集的表达谱,通过在线分析工具 GEO2R 和加权基因共表达网络分析筛选与 HCC 转移相关的差异表达基因。其次,通过单因素 Cox 回归分析、时间依赖性 ROC 曲线和最小绝对收缩和选择算子 Cox 回归分析建立包括 27-mRNA 的风险评分模型。然后,我们在队列癌症基因组图谱-肝肝细胞癌中验证了该模型,并分析了与风险评分模型相关的基因的功能和关键信号通路。根据风险评分模型,患者被分为两个亚组(高风险组和低风险组)。在训练队列中,两个亚组之间的转移率存在显著差异(<0.0001,风险比[HR]:10.3,95%置信区间[95%CI]:6.827-15.55)和外部验证队列(=0.0008,HR:1.768,95%CI:1.267-2.467)。多变量分析表明,风险评分模型在预测 HCC 早期转移方面优于并独立于其他临床因素(如肿瘤分期、肿瘤大小和其他参数)。此外,风险评分模型可预测 HCC 患者的总生存期。最后,27-mRNA 中的大多数都富集在外泌体和膜结合细胞器中,这些参与了运输和代谢的生物过程。蛋白质-蛋白质相互作用网络分析表明,这些基因中的大多数可能是影响 HCC 进展的关键基因。此外,27-mRNA 中的 3 个基因在外周血单核细胞中也有差异表达。总之,通过使用两种联合方法和更广泛的 HCC 数据集,我们的研究为 HCC 转移提供了可靠且优越的预测模型,这将有助于对这些高转移风险 HCC 患者进行个体化医疗管理。

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