ZEB2在COAD转移和免疫学中的双重作用

Jingjing Wang, Bin Lu, Simin Zeng, Liqing Li, Huiyan Zhuo, Youqiang Li
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摘要

目的:锌指E-box binding homeobox (ZEB2)被广泛认为是一种致癌基因,它可以通过诱导上游转录启动子的激活来加速细胞核DNA的复制。最近的研究发现,在肝细胞癌中,过表达ZEB2与较好的预后相关。然而,在COAD中,其在肿瘤生长、转移和免疫学中的作用尚未阐明。方法:泛癌测序数据来源于The Cancer Genome Atlas (TCGA)-Pan Cancer cohort,正常人组织数据来源于gene - type-tissue expression (GTEx)数据库,Broad Institute Cancer Cell Line Encyclopedia (CCLE)来源于UCSC Xena。我们使用cBioPortal网络工具分析和可视化ZEB2泛癌基因组变化率。GEO表达数据集用于探索COAD患者中ZEB2的表达水平。使用UCSC Xena数据库下载COAD患者的预后信息。采用Cox回归和Kaplan-Meier分析评估ZEB2在COAD中的预后作用。使用京都基因与基因组百科全书(KEGG)来确定生物学途径。进行基因本体(GO)富集分析,以确定COAD中以zeb2依赖方式改变的生物过程、分子功能和细胞成分。利用Cytoscape软件的MCODE工具对PPI相互作用网络进行模块分析,利用cytohHubba工具筛选特征分子。利用CIBERSORTx数据库分析22种免疫浸润细胞存在时ZEB2的表达。结果:本研究发现ZEB2在大多数癌症类型中表达异常,与正常组织相比,ZEB2在COAD中显著下调。此外,我们的研究结果还表明,ZEB2过表达与COAD患者更好的预后相关。机制分析显示,ZEB2的过表达与COAD中中性粒细胞胞外陷阱的形成有关。结果表明,ZEB2表达与多种免疫细胞浸润有显著相关性。结论:本研究表明,ZEB2过表达与COAD患者预后较好相关。ZEB2与ACTB关系密切,而ACTB与NETs高度相关。这些发现表明ZEB2在COAD生长、转移和免疫中的双重作用。
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The Dual Role of ZEB2 in COAD Metastasis and Immunology
Objective: The zinc finger E-box binding homeobox (ZEB2), which can accelerate the nuclear DNA replication by inducing the activation of upstream transcription promoters, was widely considered as an oncogene. Recent study has found that the overexpression of ZEB2 is associated with a better prognosis in hepatocellular carcinoma. However, its roles in tumor growth, metastasis, and immunology are yet to be elucidated in COAD. Methods: The pan-cancer sequencing data was acquired from The Cancer Genome Atlas (TCGA)-Pan cancer cohort, normal human tissue data was acquired from the Genotype-tissue expression (GTEx) database, and Broad Institute Cancer Cell Line Encyclopedia (CCLE) were downloaded from UCSC Xena. We used the cBioPortal webtool to analyze and visualize the ZEB2 pan-cancer genomic alteration rate. GEO Expression Datasets were used to explore ZEB2 expression levels in COAD patients. UCSC Xena database was used to download prognostic information of COAD patients. The Cox regression and Kaplan–Meier analyses were used to assess the prognostic role of ZEB2 in COAD. Kyoto Encyclopedia of Genes and Genomes (KEGG) was performed to determine the biological pathways. Gene Ontology (GO) enrichment analysis was performed to determine the biological processes, molecular functions, and cellular components that were altered in a ZEB2-dependent manner in COAD. The module analysis of PPI interaction network was performed using the MCODE tool of Cytoscape software, and the characteristic molecules were selected by cytohHubba tool. CIBERSORTx database was used to analyze the ZEB2 expression in the presence of 22 types of immune infiltrating cells. Results: This study found that ZEB2 was aberrantly expressed in most cancer types, and it was significantly downregulated in COAD compared with normal tissue. In addition, our findings also show that overexpression of ZEB2 was associated with a better prognosis in COAD. Mechanistic analysis revealed that overexpression of ZEB2 was associated with the neutrophil extracellular trap formation in COAD. And the results show that ZEB2 expression was significantly correlated with several kinds of immune cell infiltration. Conclusion: This study demonstrates that overexpression of ZEB2 was associated with better prognoses in patients with COAD. ZEB2 has close relationship with ACTB, which was highly related to NETs. These findings suggest a dual role of ZEB2 in COAD growth, metastasis, and immunology.
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