Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer

Background: Hypoxia is a crucial factor in the development of esophageal cancer. The relationship between hypoxia and immune status in the esophageal cancer microenvironment is becoming increasingly important in clinical practice. This study aims to clarify and investigate the possible connection b...

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Auteurs principaux: Linlin Tan, Dingzhuo Cheng, Jianbo Wen, Kefeng Huang, Qin Zhang
Format: article
Langue:EN
Publié: AIMS Press 2021
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spelling oai:doaj.org-article:b0508df6e5c943aa9e9431a3e6ec1c022021-11-23T02:39:15ZIdentification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer10.3934/mbe.20213841551-0018https://doaj.org/article/b0508df6e5c943aa9e9431a3e6ec1c022021-09-01T00:00:00Zhttps://www.aimspress.com/article/doi/10.3934/mbe.2021384https://www.aimspress.com/article/doi/10.3934/mbe.2021384https://doaj.org/toc/1551-0018Background: Hypoxia is a crucial factor in the development of esophageal cancer. The relationship between hypoxia and immune status in the esophageal cancer microenvironment is becoming increasingly important in clinical practice. This study aims to clarify and investigate the possible connection between immunotherapy and hypoxia in esophageal cancer. Methods: The Cancer Genome Atlas databases are used to find two types of esophageal cancer cases. Cox regressions analyses are used to screen genes for hypoxia-related traits. After that, the genetic signature is validated by survival analysis and the construction of ROC curves. GSEA is used to compare differences in enrichment in the two groups and is followed by the CIBERSORT tool to investigate a potentially relevant correlation between immune cells and gene signatures. Results: We found that the esophageal adenocarcinoma hypoxia model contains 3 genes (PGK1, PGM1, SLC2A3), and the esophageal squamous cell carcinoma hypoxia model contains 2 genes (EGFR, ATF3). The findings demonstrated that the survival rate of patients in the high-risk group is lower than in the lower-risk group. Furthermore, we find that three kinds of immune cells (memory activated CD4+ T cells, activated mast cells, and M2 macrophages) have a marked infiltration in the tissues of patients in the high-risk group. Moreover, we find that PD-L1 and CD244 are highly expressed in high-risk groups. Conclusions: Our data demonstrate that oxygen deprivation is correlated with prognosis and the incidence of immune cell infiltration in patients with both types of esophageal cancer, which provides an immunological perspective for the development of personalized therapy.Linlin TanDingzhuo Cheng Jianbo WenKefeng Huang Qin Zhang AIMS Pressarticlehypoxiaesophageal cancertumor microenvironmentimmune cell infiltrationgene set enrichment analysisBiotechnologyTP248.13-248.65MathematicsQA1-939ENMathematical Biosciences and Engineering, Vol 18, Iss 6, Pp 7743-7758 (2021)
institution DOAJ
collection DOAJ
language EN
topic hypoxia
esophageal cancer
tumor microenvironment
immune cell infiltration
gene set enrichment analysis
Biotechnology
TP248.13-248.65
Mathematics
QA1-939
spellingShingle hypoxia
esophageal cancer
tumor microenvironment
immune cell infiltration
gene set enrichment analysis
Biotechnology
TP248.13-248.65
Mathematics
QA1-939
Linlin Tan
Dingzhuo Cheng
Jianbo Wen
Kefeng Huang
Qin Zhang
Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
description Background: Hypoxia is a crucial factor in the development of esophageal cancer. The relationship between hypoxia and immune status in the esophageal cancer microenvironment is becoming increasingly important in clinical practice. This study aims to clarify and investigate the possible connection between immunotherapy and hypoxia in esophageal cancer. Methods: The Cancer Genome Atlas databases are used to find two types of esophageal cancer cases. Cox regressions analyses are used to screen genes for hypoxia-related traits. After that, the genetic signature is validated by survival analysis and the construction of ROC curves. GSEA is used to compare differences in enrichment in the two groups and is followed by the CIBERSORT tool to investigate a potentially relevant correlation between immune cells and gene signatures. Results: We found that the esophageal adenocarcinoma hypoxia model contains 3 genes (PGK1, PGM1, SLC2A3), and the esophageal squamous cell carcinoma hypoxia model contains 2 genes (EGFR, ATF3). The findings demonstrated that the survival rate of patients in the high-risk group is lower than in the lower-risk group. Furthermore, we find that three kinds of immune cells (memory activated CD4+ T cells, activated mast cells, and M2 macrophages) have a marked infiltration in the tissues of patients in the high-risk group. Moreover, we find that PD-L1 and CD244 are highly expressed in high-risk groups. Conclusions: Our data demonstrate that oxygen deprivation is correlated with prognosis and the incidence of immune cell infiltration in patients with both types of esophageal cancer, which provides an immunological perspective for the development of personalized therapy.
format article
author Linlin Tan
Dingzhuo Cheng
Jianbo Wen
Kefeng Huang
Qin Zhang
author_facet Linlin Tan
Dingzhuo Cheng
Jianbo Wen
Kefeng Huang
Qin Zhang
author_sort Linlin Tan
title Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
title_short Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
title_full Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
title_fullStr Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
title_full_unstemmed Identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
title_sort identification of prognostic hypoxia-related genes signature on the tumor microenvironment in esophageal cancer
publisher AIMS Press
publishDate 2021
url https://doaj.org/article/b0508df6e5c943aa9e9431a3e6ec1c02
work_keys_str_mv AT linlintan identificationofprognostichypoxiarelatedgenessignatureonthetumormicroenvironmentinesophagealcancer
AT dingzhuocheng identificationofprognostichypoxiarelatedgenessignatureonthetumormicroenvironmentinesophagealcancer
AT jianbowen identificationofprognostichypoxiarelatedgenessignatureonthetumormicroenvironmentinesophagealcancer
AT kefenghuang identificationofprognostichypoxiarelatedgenessignatureonthetumormicroenvironmentinesophagealcancer
AT qinzhang identificationofprognostichypoxiarelatedgenessignatureonthetumormicroenvironmentinesophagealcancer
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