Zhang Dongdong, Wang Wenyan, Zhou Huandi, Su Linlin, Han Xuetao, Zhang Xinyuan, Han Wei, Wang Yu, Xue Xiaoying
Department of Radiotherapy, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Department of Central Laboratory, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Front Genet. 2022 May 31;13:851505. doi: 10.3389/fgene.2022.851505. eCollection 2022.
The expression, prognosis, and related mechanisms of ANXA1 are investigated in glioma, with the objective to find potential therapeutic molecular targets for glioma. We analyzed the gene expression of ANXA1 using glioma-related databases, including the Chinese Glioma Genome Atlas (CGGA) database, The Cancer Genome Atlas (TCGA) database, and the Gene Expression Omnibus (GEO) database. Moreover, we collected the sample tissues and corresponding paracancerous tissues of 23 glioma patients and then conducted a Western blot experiment to verify the expression and correlate survival of ANXA1. Moreover, we generated survival ROC curves, performing univariate and multivariate Cox analyses and the construction of the nomogram. Differential expression analysis was conducted by high and low grouping based on the median of the ANXA1 gene expression values. We conducted Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis and Gene Set Enrichment Analysis (GSEA) to explore possible mechanisms, and gene co-expression analysis was also performed. The results showed that the ANXA1 expression level was higher in gliomas than in normal tissues, and a high expression level of ANXA1 in gliomas was associated with poorer prognosis. The independent prognosis analysis showed that the ANXA1 gene was an independent prognostic factor of glioma. In the analysis of KEGG and Gene Set Enrichment Analysis (GSEA), it is shown that ANXA1 may play an important role in glioma patients by affecting extracellular matrix (ECM)-receptor interaction and the focal adhesion signal pathway. The core genes, including COL1A1, COL1A2, FN1, ITGA1, and ITGB1, were screened for gene correlation and prognosis analysis. The expression level of the five genes was verified by qPCR in glioma. We concluded that these five core genes and ANXA1 could play a synergistic role in gliomas. The results indicated that a high expression level of ANXA1 leads to worse prognosis and ANXA1 is an independent prognostic factor and a potentially important target for the treatment of gliomas.
研究了膜联蛋白A1(ANXA1)在胶质瘤中的表达、预后及相关机制,旨在寻找胶质瘤潜在的治疗分子靶点。我们利用胶质瘤相关数据库分析了ANXA1的基因表达,包括中国胶质瘤基因组图谱(CGGA)数据库、癌症基因组图谱(TCGA)数据库和基因表达综合数据库(GEO)。此外,我们收集了23例胶质瘤患者的样本组织及相应癌旁组织,然后进行蛋白质免疫印迹实验以验证ANXA1的表达并关联其生存情况。此外,我们生成了生存ROC曲线,进行单因素和多因素Cox分析并构建列线图。基于ANXA1基因表达值的中位数进行高低分组,进行差异表达分析。我们进行了京都基因与基因组百科全书(KEGG)富集分析和基因集富集分析(GSEA)以探索可能的机制,还进行了基因共表达分析。结果显示,胶质瘤中ANXA1的表达水平高于正常组织,且胶质瘤中ANXA1的高表达与较差的预后相关。独立预后分析表明,ANXA1基因是胶质瘤的独立预后因素。在KEGG和基因集富集分析(GSEA)中显示,ANXA1可能通过影响细胞外基质(ECM)-受体相互作用和粘着斑信号通路在胶质瘤患者中发挥重要作用。筛选了包括COL1A1、COL1A2、FN1、ITGA1和ITGB1在内的核心基因进行基因相关性和预后分析。通过qPCR在胶质瘤中验证了这五个基因的表达水平。我们得出结论,这五个核心基因与ANXA1可能在胶质瘤中发挥协同作用。结果表明,ANXA1的高表达导致预后较差,且ANXA1是独立的预后因素及治疗胶质瘤潜在的重要靶点。