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烯醇化酶1与多种癌症类型的癌症进展和免疫浸润相关:一项泛癌分析

Enolase 1 Correlated With Cancer Progression and Immune-Infiltrating in Multiple Cancer Types: A Pan-Cancer Analysis.

作者信息

Xu Wenhua, Yang Wenna, Wu Chunfeng, Ma Xiaocong, Li Haoyu, Zheng Jinghui

机构信息

Department of Cardiology, Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, China.

Graduate School, Guangxi University of Chinese Medicine, Nanning City, China.

出版信息

Front Oncol. 2021 Feb 10;10:593706. doi: 10.3389/fonc.2020.593706. eCollection 2020.

DOI:10.3389/fonc.2020.593706
PMID:33643901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7902799/
Abstract

Enolase 1 (ENO1) is an oxidative stress protein expressed in endothelial cells. This study aimed to investigate the correlation of ENO1 with prognosis, tumor stage, and levels of tumor-infiltrating immune cells in multiple cancers. ENO1 expression and its influence on tumor stage and clinical prognosis were analyzed by UCSC Xena browser, Gene Expression Profiling Interactive Analysis (GEPIA), The Cancer Genome Atlas (TCGA), and GTEx Portal. The ENO1 mutation analysis was performed by cBio Portal, and demonstrated ENO1 mutation (1.8%) did not impact on tumor prognosis. The relationship between ENO1 expression and tumor immunity was analyzed by Tumor Immune Estimation Resource (TIMER) and GEPIA. The potential functions of ENO1 in pathways were investigated by Gene Set Enrichment Analysis. ENO1 expression was significantly different in tumor and corresponding normal tissues. ENO1 expression in multiple tumor tissues correlated with prognosis and stage. ENO1 showed correlation with immune infiltrates including B cells, CD8 and CD4 T cells, macrophages, neutrophils, and dendritic cells, and tumor purity. ENO1 was proved to be involved in DNA replication, cell cycle, apoptosis, glycolysis process, and other processes. These findings indicate that ENO1 is a potential prognostic biomarker that correlates with cancer progression immune infiltration.

摘要

烯醇化酶1(ENO1)是一种在内皮细胞中表达的氧化应激蛋白。本研究旨在探讨ENO1与多种癌症的预后、肿瘤分期及肿瘤浸润免疫细胞水平之间的相关性。通过UCSC Xena浏览器、基因表达谱交互式分析(GEPIA)、癌症基因组图谱(TCGA)和GTEx数据库分析ENO1的表达及其对肿瘤分期和临床预后的影响。通过cBio数据库进行ENO1突变分析,结果显示ENO1突变(1.8%)对肿瘤预后无影响。通过肿瘤免疫评估资源(TIMER)和GEPIA分析ENO1表达与肿瘤免疫的关系。通过基因集富集分析研究ENO1在各通路中的潜在功能。ENO1在肿瘤组织和相应正常组织中的表达存在显著差异。多种肿瘤组织中ENO1的表达与预后和分期相关。ENO1与包括B细胞、CD8和CD4 T细胞、巨噬细胞、中性粒细胞和树突状细胞在内的免疫浸润以及肿瘤纯度相关。ENO1被证明参与DNA复制、细胞周期、凋亡、糖酵解过程等。这些发现表明,ENO1是一种与癌症进展免疫浸润相关的潜在预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/7b2885fd2d63/fonc-10-593706-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/9df7269aea8f/fonc-10-593706-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/63490889ff15/fonc-10-593706-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/cc81aaaf2a2f/fonc-10-593706-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/7b2885fd2d63/fonc-10-593706-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/9df7269aea8f/fonc-10-593706-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/68acc76dc9b7/fonc-10-593706-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/ddf534c6922e/fonc-10-593706-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/ac6a79de193a/fonc-10-593706-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/63490889ff15/fonc-10-593706-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/cc81aaaf2a2f/fonc-10-593706-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5788/7902799/7b2885fd2d63/fonc-10-593706-g009.jpg

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ENO1 Acts as a Prognostic Biomarker Candidate and Promotes Tumor Growth and Migration Ability Through the Regulation of Rab1A in Colorectal Cancer.
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ENO1 as a Biomarker of Breast Cancer Progression and Metastasis: A Bioinformatic Approach Using Available Databases.ENO1作为乳腺癌进展和转移的生物标志物:一种利用现有数据库的生物信息学方法
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