Yang Lingpeng, He Yang, Zhang Zifei, Wang Wentao
Department of Liver Surgery & Liver Transplantation Center, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
PeerJ. 2019 Dec 9;7:e8245. doi: 10.7717/peerj.8245. eCollection 2019.
Growing evidence showed that alternative splicing (AS) event is significantly related to tumor occurrence and progress. This study was performed to make a systematic analysis of AS events and constructed a robust prediction model of hepatocellular carcinoma (HCC). The clinical information and the genes expression profile data of 335 HCC patients were collected from The Cancer Genome Atlas (TCGA). Information of seven types AS events were collected from the TCGA SpliceSeq database. Overall survival (OS) related AS events and splicing factors (SFs) were identified using univariate Cox regression analysis. The corresponding genes of OS-related AS events were sent for gene network analysis and functional enrichment analysis. Optimal OS-related AS events were selected by LASSO regression to construct prediction model using multivariate Cox regression analysis. Prognostic value of the prediction models were assessed by receiver operating characteristic (ROC) curve and KaplanMeir survival analysis. The relationship between the Percent Spliced In (PSI) value of OS-related AS events and SFs expression were analyzed using Spearman correlation analysis. And the regulation network was generated by Cytoscape. A total of 34,163 AS events were identified, which consist of 3,482 OS-related AS events. UBB, UBE2D3, SF3A1 were the hub genes in the gene network of the top 800 OS-related AS events. The area under the curve (AUC) of the final prediction model based on seven types OS-related AS events was 0.878, 0.843, 0.821 in 1, 3, 5 years, respectively. Upon multivariate analysis, risk score (All) served as the risk factor to independently predict OS for HCC patients. SFs HNRNPH3 and HNRNPL were overexpressed in tumor samples and were signifcantly associated with the OS of HCC patients. The regulation network showed prominent correlation between the expression of SFs and OS-related AS events in HCC patients. The final prediction model performs well in predicting the prognosis of HCC patients. And the findings in this study improve our understanding of the association between AS events and HCC.
越来越多的证据表明,可变剪接(AS)事件与肿瘤的发生和进展密切相关。本研究旨在对AS事件进行系统分析,并构建一个强大的肝细胞癌(HCC)预测模型。从癌症基因组图谱(TCGA)收集了335例HCC患者的临床信息和基因表达谱数据。从TCGA SpliceSeq数据库收集了七种类型AS事件的信息。使用单变量Cox回归分析确定总生存期(OS)相关的AS事件和剪接因子(SFs)。将OS相关AS事件的相应基因送去进行基因网络分析和功能富集分析。通过LASSO回归选择最佳的OS相关AS事件,使用多变量Cox回归分析构建预测模型。通过受试者工作特征(ROC)曲线和Kaplan-Meir生存分析评估预测模型的预后价值。使用Spearman相关分析分析OS相关AS事件的剪接百分率(PSI)值与SFs表达之间的关系。并通过Cytoscape生成调控网络。共鉴定出34163个AS事件,其中包括3482个OS相关AS事件。UBB、UBE2D3、SF3A1是前800个OS相关AS事件的基因网络中的枢纽基因。基于七种类型OS相关AS事件的最终预测模型在1年、3年、5年的曲线下面积(AUC)分别为0.878、0.843、0.821。多变量分析显示,风险评分(All)作为独立预测HCC患者OS的危险因素。SFs HNRNPH3和HNRNPL在肿瘤样本中过表达,且与HCC患者的OS显著相关。调控网络显示HCC患者中SFs的表达与OS相关AS事件之间存在显著相关性。最终预测模型在预测HCC患者预后方面表现良好。本研究结果提高了我们对AS事件与HCC之间关联的理解。