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真核生物翻译起始因子3亚基B在肝癌中的表达及其预后意义。

Expression of eukaryotic translation initiation factor 3 subunit B in liver cancer and its prognostic significance.

作者信息

Yue Qing, Meng Lingyu, Jia Baoxing, Han Wei

机构信息

Department of Oncology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

Department of Hepatobiliary and Pancreatic Surgery, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

出版信息

Exp Ther Med. 2020 Jul;20(1):436-446. doi: 10.3892/etm.2020.8726. Epub 2020 May 7.

Abstract

Liver cancer is one of the major malignancies with the worst prognosis among all solid tumor types. It is therefore ponderable to explore prognostic biomarkers and therapeutic targets for liver cancer. Eukaryotic translation initiation factor 3 subunit B (EIF3B) is closely linked to the transcription initiation of cancer-associated genes. In the present study, EIF3B was indicated to be a potential prognostic biomarker of liver cancer. The mRNA expression level of EIF3B in liver cancer was assessed by analyzing the Cancer Genome Atlas dataset. χ and Fisher's exact tests were used to assess the association of EIF3B expression with clinical parameters. Receiver-operating characteristic curve analysis was used for evaluating the diagnostic value of EIF3B. Overall and relapse-free survival were assessed using Kaplan-Meier curves to determine the association between EIF3B expression and survival. Univariate and multivariate Cox regression analysis were performed to identify the factors affecting overall/relapse-free survival. Gene set enrichment analysis (GSEA) was used to identify signaling pathways associated with EIF3B in liver cancer. It was revealed that EIF3B was highly expressed in liver cancer tissues and it had a promising diagnostic ability. Furthermore, the survival analysis indicated that patients with high EIF3B expression generally had shorter overall as well as relapse-free survival. Univariate and multivariate Cox analysis suggested that high EIF3B mRNA expression may serve as an independent biomarker for the prognostication of patients with liver cancer. GSEA suggested that MYC-V1 (HALLMARK_MYC_TARGETS_V1 geneset; P=0.009), MYC-V2 (HALLMARK_MYC_TARGETS_V2 geneset; P=0.004) and DNA repair pathways (HALLMARK_DNA_REPAIR geneset; P<0.001) were differentially enriched in high EIF3B expression and low EIF3B expression groups. In conclusion, high EIF3B expression was indicated to be an independent prognostic biomarker for patients with liver cancer.

摘要

肝癌是所有实体瘤类型中预后最差的主要恶性肿瘤之一。因此,探索肝癌的预后生物标志物和治疗靶点是值得思考的。真核翻译起始因子3亚基B(EIF3B)与癌症相关基因的转录起始密切相关。在本研究中,EIF3B被表明是肝癌的一种潜在预后生物标志物。通过分析癌症基因组图谱数据集评估肝癌中EIF3B的mRNA表达水平。采用χ检验和Fisher精确检验评估EIF3B表达与临床参数的相关性。采用受试者工作特征曲线分析评估EIF3B的诊断价值。使用Kaplan-Meier曲线评估总生存期和无复发生存期,以确定EIF3B表达与生存之间的关联。进行单因素和多因素Cox回归分析,以确定影响总生存期/无复发生存期的因素。基因集富集分析(GSEA)用于确定肝癌中与EIF3B相关的信号通路。结果显示,EIF3B在肝癌组织中高表达,具有良好的诊断能力。此外,生存分析表明,EIF3B高表达的患者总体生存期和无复发生存期通常较短。单因素和多因素Cox分析表明,EIF3B mRNA高表达可能作为肝癌患者预后的独立生物标志物。GSEA表明,MYC-V1(HALLMARK_MYC_TARGETS_V1基因集;P=0.009)、MYC-V2(HALLMARK_MYC_TARGETS_V2基因集;P=0.004)和DNA修复通路(HALLMARK_DNA_REPAIR基因集;P<0.001)在EIF3B高表达组和低表达组中差异富集。总之,EIF3B高表达被表明是肝癌患者的独立预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f180/7282191/0fa7d2c4db26/etm-20-01-0436-g00.jpg

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