Comprehensive Analysis of the Prognostic Values of the TRIM Family in Hepatocellular Carcinoma

肝细胞癌 接收机工作特性 比例危险模型 列线图 修剪 医学 肿瘤科 肝癌 生存分析 基因 癌症研究 内科学 生物 遗传学 计算机科学 操作系统
作者
Weiyu Dai,Jing Wang,Wang Zhi,Yizhi Xiao,Jiaying Li,Linjie Hong,Miaomiao Pei,Jieming Zhang,Ping Yang,Xiaosheng Wu,Weimei Tang,Xiaoling Jiang,Ping Jiang,Xiang Li,Aimin Li,Jing Lin,Side Liu
出处
期刊:Frontiers in Oncology [Frontiers Media SA]
卷期号:11 被引量:10
标识
DOI:10.3389/fonc.2021.767644
摘要

Background Accumulating studies have demonstrated the abnormal expressions and prognostic values of certain members of the tripartite motif (TRIM) family in diverse cancers. However, comprehensive prognostic values of the TRIM family in hepatocellular carcinoma (HCC) are yet to be clearly defined. Methods The prognostic values of the TRIM family were evaluated by survival analysis and univariate Cox regression analysis based on gene expression data and clinical data of HCC from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. The expression profiles, protein–protein interaction among the TRIM family, prediction of transcription factors (TFs) or miRNAs, genetic alterations, correlations with the hallmarks of cancer and immune infiltrates, and pathway enrichment analysis were explored by multiple public databases. Further, a TRIM family gene-based signature for predicting overall survival (OS) in HCC was built by using the least absolute shrinkage and selection operator (LASSO) regression. TCGA–Liver Hepatocellular Carcinoma (LIHC) cohort was used as the training set, and GSE76427 was used for external validation. Time-dependent receiver operating characteristic (ROC) and survival analysis were used to estimate the signature. Finally, a nomogram combining the TRIM family risk score and clinical parameters was established. Results High expressions of TRIM family members including TRIM3, TRIM5, MID1, TRIM21, TRIM27, TRIM32, TRIM44, TRIM47, and TRIM72 were significantly associated with HCC patients’ poor OS. A novel TRIM family gene-based signature (including TRIM5, MID1, TRIM21, TRIM32, TRIM44, and TRIM47) was built for OS prediction in HCC. ROC curves suggested the signature’s good performance in OS prediction. HCC patients in the high-risk group had poorer OS than the low-risk patients based on the signature. A nomogram integrating the TRIM family risk score, age, and TNM stage was established. The ROC curves suggested that the signature presented better discrimination than the similar model without the TRIM family risk score. Conclusion Our study identified the potential application values of the TRIM family for outcome prediction in HCC.
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