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基于共表达分析鉴定与肝细胞癌进展相关的三个关键基因

Identification of Three Key Genes Associated with Hepatocellular Carcinoma Progression Based on Co-expression Analysis.

作者信息

Lin Jinhui, Zhang Fangfang

机构信息

The Department of Oncology Intervention, Taizhou Municipal Hospital, Taizhou, 318000, Zhejiang Province, China.

The Department of Pathology, Taizhou Municipal Hospital, Taizhou, 318000, Zhejiang Province, China.

出版信息

Cell Biochem Biophys. 2022 Jun;80(2):301-309. doi: 10.1007/s12013-021-01028-2. Epub 2021 Aug 18.

Abstract

Hepatocellular carcinoma (HCC) is the fifth most common cancer and one of the leading causes of cancer-related death in the world. Due to the recurrence of HCC, its survival rate is still low. Therefore, it is vital to seek prognostic biomarkers for HCC. In this study, differential analysis was conducted on gene expression data in The Cancer Genome Atlas -LIHC, and 4482 differentially expressed genes in tumor tissue were selected. Then, weighted gene co-expression network analysis was used to analyze the co-expression of the gained differential genes. By module-trait correlation analysis, the turquoise gene module that was significantly related to tumor grade, pathologic_T stage, and clinical stage was identified. Thereafter, enrichment analysis of genes in this module uncovered that the genes were mainly enriched in the signaling pathways involved in spliceosome and cell cycle. After that, through correlation analysis, 18 hub genes highly correlated with tumor grade, clinical stage, pathologic_T stage, and the turquoise module were selected. Meanwhile, protein-protein interaction (PPI) network was constructed by using genes in the module. Finally, three key genes, heterogeneous nuclear ribonucleoprotein L, serrate RNA effector molecule, and cyclin B2, were identified by intersecting the top 30 genes with the highest connectivity in PPI network and the previously obtained 18 hub genes in the turquoise module. Further survival analysis revealed that high expression of the three key genes predicted poor prognosis of HCC. These results indicated the direction for further research on clinical diagnosis and prognostic biomarkers of HCC.

摘要

肝细胞癌(HCC)是全球第五大常见癌症,也是癌症相关死亡的主要原因之一。由于HCC会复发,其生存率仍然很低。因此,寻找HCC的预后生物标志物至关重要。在本研究中,对癌症基因组图谱-LIHC中的基因表达数据进行了差异分析,筛选出肿瘤组织中4482个差异表达基因。然后,使用加权基因共表达网络分析来分析获得的差异基因的共表达情况。通过模块-性状相关性分析,确定了与肿瘤分级、病理T分期和临床分期显著相关的蓝绿色基因模块。此后,对该模块中的基因进行富集分析发现,这些基因主要富集在与剪接体和细胞周期相关的信号通路中。之后,通过相关性分析,筛选出与肿瘤分级、临床分期、病理T分期以及蓝绿色模块高度相关的18个核心基因。同时,利用该模块中的基因构建了蛋白质-蛋白质相互作用(PPI)网络。最后,通过将PPI网络中连接性最高的前30个基因与之前在蓝绿色模块中获得的18个核心基因进行交叉,确定了三个关键基因,即不均一核核糖核蛋白L、锯齿状RNA效应分子和细胞周期蛋白B2。进一步的生存分析表明,这三个关键基因的高表达预示着HCC患者预后不良。这些结果为HCC临床诊断和预后生物标志物的进一步研究指明了方向。

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