Nie Zhi, Pu Tong, Han Zhaojie, Wang Chenyang, Pan Chenglong, Li Ping, Ma Xiaoling, Yao Yanfei, Zhao Youmei, Wang Chunyan, Jiang Xiulin, Ding Jianyang
Department of Neurology, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Department of Neurology, Yunnan Province Clinical Research Center for Neurological Diseases, Kunming, China.
Front Oncol. 2022 Jun 22;12:930647. doi: 10.3389/fonc.2022.930647. eCollection 2022.
Extra spindle pole bodies-like 1 (ESPL1), a cysteine endopeptidase, plays a vital role in chromosome inheritance. However, the association of ESPL1 with prognosis and immune infiltration in lung adenocarcinoma (LUAD) has not yet been explored. Here, we analyzed the expression level, prognostic values, diagnostic value, and immune infiltration level in LUAD using various databases. Immunohistochemistry (IHC) and quantitative real-time PCR (qRT-PCR) assays were used to detect the expression of ESPL1 in LUAD tissues and cell lines. In this study, we found that ESPL1 was upregulated in LUAD and a higher expression of ESPL1 was correlated with unfavorable prognosis in LUAD. Meanwhile, Cox hazard regression analysis results suggested that ESPL1 may be an independent prognostic factor for LUAD. Moreover, we demonstrated that ESPL1 expression was significantly correlated with immune infiltration of Th2 and dendritic cells in LUAD. We also confirmed that DNA copy number amplification and DNA hypo-methylation were positively correlated with ESPL1 expression in LUAD. Additionally, DNA copy number amplification was significantly associated with adverse clinical outcomes in LUAD. Kyoto Encyclopedia of Genes and Genomes (KEGG) and gene set enrichment analysis (GSEA) confirmed that ESPL1 was mainly involved in the DNA replication and glycolysis signaling pathway. Finally, we revealed that ESPL1 was highly expressed in LUAD tissues and cell lines. Knockdown of ESPL1 significantly inhibited cell migration and the invasion abilities of LUAD. Our study comprehensively confirmed that ESPL1 expression may serve as a novel prognostic biomarker for both the clinical outcome and immune cell infiltration in LUAD.
类额外纺锤极体蛋白1(ESPL1)是一种半胱氨酸内肽酶,在染色体遗传中起着至关重要的作用。然而,ESPL1与肺腺癌(LUAD)预后及免疫浸润的相关性尚未得到研究。在此,我们利用各种数据库分析了LUAD中的表达水平、预后价值、诊断价值及免疫浸润水平。采用免疫组织化学(IHC)和定量实时PCR(qRT-PCR)检测LUAD组织和细胞系中ESPL1的表达。在本研究中,我们发现ESPL1在LUAD中上调,且ESPL1的高表达与LUAD的不良预后相关。同时,Cox风险回归分析结果表明ESPL1可能是LUAD的一个独立预后因素。此外,我们证明ESPL1表达与LUAD中Th2和树突状细胞的免疫浸润显著相关。我们还证实DNA拷贝数扩增和DNA低甲基化与LUAD中ESPL1表达呈正相关。此外,DNA拷贝数扩增与LUAD的不良临床结局显著相关。京都基因与基因组百科全书(KEGG)和基因集富集分析(GSEA)证实ESPL1主要参与DNA复制和糖酵解信号通路。最后,我们发现ESPL1在LUAD组织和细胞系中高表达。敲低ESPL1可显著抑制LUAD的细胞迁移和侵袭能力。我们的研究全面证实ESPL1表达可能作为LUAD临床结局和免疫细胞浸润的一种新型预后生物标志物。