Effects of Inflammation on the Immune Microenvironment in Gastric Cancer

BackgroundChronic inflammation and immune cell dysfunction in the tumor microenvironment are key factors in the development and progression of gastric tumors. However, inflammation-related genes associated with gastric cancer prognosis and their relationship with the expression of immune genes are n...

Full description

Bibliographic Details
Main Authors: Weidan Zhao, Mingqing Liu, Mingyue Zhang, Yachen Wang, Yingli Zhang, Shiji Wang, Nan Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.690298/full
_version_ 1818917926929956864
author Weidan Zhao
Mingqing Liu
Mingyue Zhang
Yachen Wang
Yingli Zhang
Shiji Wang
Nan Zhang
author_facet Weidan Zhao
Mingqing Liu
Mingyue Zhang
Yachen Wang
Yingli Zhang
Shiji Wang
Nan Zhang
author_sort Weidan Zhao
collection DOAJ
description BackgroundChronic inflammation and immune cell dysfunction in the tumor microenvironment are key factors in the development and progression of gastric tumors. However, inflammation-related genes associated with gastric cancer prognosis and their relationship with the expression of immune genes are not fully understood.MethodIn this study, we established an inflammatory response model score called “Riskscore”, based on differentially expressed genes in gastric cancer. We used Survival and Survminer packages in R to analyze patient survival and prognosis in risk groups. The survival curve was plotted using the Kaplan–Meier method, and the log-rank test was used to assess statistical significance, and we performed the ROC analysis using the R language package to analyze the 1-, 3-, and 5-year survival of patients in the GEO and TCGA databases. Single-factor and multi-factor prognostic analyses were carried out for age, sex, T, N, M, and risk score. Pathway enrichment analysis indicated immune factor-related pathway enrichment in both patient groups. Next, we screened for important genes that are involved in immune cell regulation. Finally, we created a correlation curve to explore the correlation between Riskscore and the expression of these genes.ResultsThe prognosis was significantly different between high- and low-risk groups, and the survival rate and survival time of the high-risk group were lower than those of the low-risk group. we found that the pathways related to apoptosis, hypoxia, and immunity were most enriched in the risk groups. we found two common tumor-infiltrating immune cell types (i.e., follicular helper T cells and resting dendritic cells) between the two risk groups and identified 10 genes that regulate these cells. Additionally, we found that these 10 genes are positively associated with the two risk groups.ConclusionFinally, a risk model of the inflammatory response in gastric cancer was established, and the inflammation-related genes used to construct the model were found to be directly related to immune infiltration. This model can improve the gastric cancer prognosis prediction. Our findings contribute to the development of immunotherapy for the treatment of gastric cancer patients.
first_indexed 2024-12-20T00:41:50Z
format Article
id doaj.art-7c6917d47247481db3827d7abac770d3
institution Directory Open Access Journal
issn 2234-943X
language English
last_indexed 2024-12-20T00:41:50Z
publishDate 2021-07-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Oncology
spelling doaj.art-7c6917d47247481db3827d7abac770d32022-12-21T19:59:32ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-07-011110.3389/fonc.2021.690298690298Effects of Inflammation on the Immune Microenvironment in Gastric CancerWeidan Zhao0Mingqing Liu1Mingyue Zhang2Yachen Wang3Yingli Zhang4Shiji Wang5Nan Zhang6Department of Gastroenterology, The First Hospital of Jilin University, Changchun, ChinaDepartment of Gastroenterology, The First Hospital of Jilin University, Changchun, ChinaDepartment of Gastroenterology, The First Hospital of Jilin University, Changchun, ChinaDepartment of Gastroenterology, The First Hospital of Jilin University, Changchun, ChinaDepartment of Gastroenterology, The First Hospital of Jilin University, Changchun, ChinaDepartment of Intensive Care Unit, The First Hospital of Jilin University, Changchun, ChinaDepartment of Gastroenterology, The First Hospital of Jilin University, Changchun, ChinaBackgroundChronic inflammation and immune cell dysfunction in the tumor microenvironment are key factors in the development and progression of gastric tumors. However, inflammation-related genes associated with gastric cancer prognosis and their relationship with the expression of immune genes are not fully understood.MethodIn this study, we established an inflammatory response model score called “Riskscore”, based on differentially expressed genes in gastric cancer. We used Survival and Survminer packages in R to analyze patient survival and prognosis in risk groups. The survival curve was plotted using the Kaplan–Meier method, and the log-rank test was used to assess statistical significance, and we performed the ROC analysis using the R language package to analyze the 1-, 3-, and 5-year survival of patients in the GEO and TCGA databases. Single-factor and multi-factor prognostic analyses were carried out for age, sex, T, N, M, and risk score. Pathway enrichment analysis indicated immune factor-related pathway enrichment in both patient groups. Next, we screened for important genes that are involved in immune cell regulation. Finally, we created a correlation curve to explore the correlation between Riskscore and the expression of these genes.ResultsThe prognosis was significantly different between high- and low-risk groups, and the survival rate and survival time of the high-risk group were lower than those of the low-risk group. we found that the pathways related to apoptosis, hypoxia, and immunity were most enriched in the risk groups. we found two common tumor-infiltrating immune cell types (i.e., follicular helper T cells and resting dendritic cells) between the two risk groups and identified 10 genes that regulate these cells. Additionally, we found that these 10 genes are positively associated with the two risk groups.ConclusionFinally, a risk model of the inflammatory response in gastric cancer was established, and the inflammation-related genes used to construct the model were found to be directly related to immune infiltration. This model can improve the gastric cancer prognosis prediction. Our findings contribute to the development of immunotherapy for the treatment of gastric cancer patients.https://www.frontiersin.org/articles/10.3389/fonc.2021.690298/fullinflammationtumor microenvironmentgastric cancerimmune cell infiltrationrisk score
spellingShingle Weidan Zhao
Mingqing Liu
Mingyue Zhang
Yachen Wang
Yingli Zhang
Shiji Wang
Nan Zhang
Effects of Inflammation on the Immune Microenvironment in Gastric Cancer
Frontiers in Oncology
inflammation
tumor microenvironment
gastric cancer
immune cell infiltration
risk score
title Effects of Inflammation on the Immune Microenvironment in Gastric Cancer
title_full Effects of Inflammation on the Immune Microenvironment in Gastric Cancer
title_fullStr Effects of Inflammation on the Immune Microenvironment in Gastric Cancer
title_full_unstemmed Effects of Inflammation on the Immune Microenvironment in Gastric Cancer
title_short Effects of Inflammation on the Immune Microenvironment in Gastric Cancer
title_sort effects of inflammation on the immune microenvironment in gastric cancer
topic inflammation
tumor microenvironment
gastric cancer
immune cell infiltration
risk score
url https://www.frontiersin.org/articles/10.3389/fonc.2021.690298/full
work_keys_str_mv AT weidanzhao effectsofinflammationontheimmunemicroenvironmentingastriccancer
AT mingqingliu effectsofinflammationontheimmunemicroenvironmentingastriccancer
AT mingyuezhang effectsofinflammationontheimmunemicroenvironmentingastriccancer
AT yachenwang effectsofinflammationontheimmunemicroenvironmentingastriccancer
AT yinglizhang effectsofinflammationontheimmunemicroenvironmentingastriccancer
AT shijiwang effectsofinflammationontheimmunemicroenvironmentingastriccancer
AT nanzhang effectsofinflammationontheimmunemicroenvironmentingastriccancer