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Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus
Barrett's esophagus (BE) is a well-known precancerous condition of esophageal adenocarcinoma. However, the immune cells and immune related genes involved in BE development and progression are not fully understood. Therefore, our study attempted to investigate the roles of immune cells and immun...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163054/ https://www.ncbi.nlm.nih.gov/pubmed/35654816 http://dx.doi.org/10.1038/s41598-022-13200-6 |
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author | Shi, Lin Guo, Renwei Chen, Zhuo Jiao, Ruonan Zhang, Shuangshuang Xiong, Xuanxuan |
author_facet | Shi, Lin Guo, Renwei Chen, Zhuo Jiao, Ruonan Zhang, Shuangshuang Xiong, Xuanxuan |
author_sort | Shi, Lin |
collection | PubMed |
description | Barrett's esophagus (BE) is a well-known precancerous condition of esophageal adenocarcinoma. However, the immune cells and immune related genes involved in BE development and progression are not fully understood. Therefore, our study attempted to investigate the roles of immune cells and immune related genes in BE patients. The raw gene expression data were downloaded from the GEO database. The limma package in R was used to screen differentially expressed genes (DEGs). Then we performed the least absolute shrinkage and selection operator (LASSO) and random forest (RF) analyses to screen key genes. The proportion of infiltrated immune cells was evaluated using the CIBERSORT algorithm between BE and normal esophagus (NE) samples. The spearman index was used to show the correlations of immune genes and immune cells. Receiver operating characteristic (ROC) curves were used to assess the diagnostic value of key genes in BE. A total of 103 differentially expressed immune-related genes were identified between BE samples and normal samples. Then, 7 genes (CD1A, LTF, FABP4, PGC, TCF7L2, INSR,SEMA3C) were obtained after Lasso analysis and RF modeling. CIBERSORT analysis revealed that resting CD4 T memory cells and gamma delta T cells were present at significantly lower levels in BE samples. Moreover, plasma cell and regulatory T cells were present at significantly higher levels in BE samples than in NE samples. INSR had the highest AUC values in ROC analysis. We identified 7 immune related genes and 4 different immune cells in our study, that may play vital roles in the occurrence and development of BE. Our findings improve the understanding of the molecular mechanisms of BE. |
format | Online Article Text |
id | pubmed-9163054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91630542022-06-05 Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus Shi, Lin Guo, Renwei Chen, Zhuo Jiao, Ruonan Zhang, Shuangshuang Xiong, Xuanxuan Sci Rep Article Barrett's esophagus (BE) is a well-known precancerous condition of esophageal adenocarcinoma. However, the immune cells and immune related genes involved in BE development and progression are not fully understood. Therefore, our study attempted to investigate the roles of immune cells and immune related genes in BE patients. The raw gene expression data were downloaded from the GEO database. The limma package in R was used to screen differentially expressed genes (DEGs). Then we performed the least absolute shrinkage and selection operator (LASSO) and random forest (RF) analyses to screen key genes. The proportion of infiltrated immune cells was evaluated using the CIBERSORT algorithm between BE and normal esophagus (NE) samples. The spearman index was used to show the correlations of immune genes and immune cells. Receiver operating characteristic (ROC) curves were used to assess the diagnostic value of key genes in BE. A total of 103 differentially expressed immune-related genes were identified between BE samples and normal samples. Then, 7 genes (CD1A, LTF, FABP4, PGC, TCF7L2, INSR,SEMA3C) were obtained after Lasso analysis and RF modeling. CIBERSORT analysis revealed that resting CD4 T memory cells and gamma delta T cells were present at significantly lower levels in BE samples. Moreover, plasma cell and regulatory T cells were present at significantly higher levels in BE samples than in NE samples. INSR had the highest AUC values in ROC analysis. We identified 7 immune related genes and 4 different immune cells in our study, that may play vital roles in the occurrence and development of BE. Our findings improve the understanding of the molecular mechanisms of BE. Nature Publishing Group UK 2022-06-02 /pmc/articles/PMC9163054/ /pubmed/35654816 http://dx.doi.org/10.1038/s41598-022-13200-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Shi, Lin Guo, Renwei Chen, Zhuo Jiao, Ruonan Zhang, Shuangshuang Xiong, Xuanxuan Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus |
title | Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus |
title_full | Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus |
title_fullStr | Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus |
title_full_unstemmed | Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus |
title_short | Analysis of immune related gene expression profiles and immune cell components in patients with Barrett esophagus |
title_sort | analysis of immune related gene expression profiles and immune cell components in patients with barrett esophagus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163054/ https://www.ncbi.nlm.nih.gov/pubmed/35654816 http://dx.doi.org/10.1038/s41598-022-13200-6 |
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