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A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer
BACKGROUND: Identifying reliable biomarkers could effectively predict esophagus carcinoma (EC) patients with poor prognosis. In this work, we constructed an immune-related gene pairs (IRGP) signature to evaluate the prognosis of EC. RESULTS: The IRGP signature was trained by the TCGA cohort and vali...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332031/ https://www.ncbi.nlm.nih.gov/pubmed/37430202 http://dx.doi.org/10.1186/s12864-023-09496-x |
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author | Zheng, Wei Fang, Gaofeng Huang, Qiao Shi, Dan Xie, Biao |
author_facet | Zheng, Wei Fang, Gaofeng Huang, Qiao Shi, Dan Xie, Biao |
author_sort | Zheng, Wei |
collection | PubMed |
description | BACKGROUND: Identifying reliable biomarkers could effectively predict esophagus carcinoma (EC) patients with poor prognosis. In this work, we constructed an immune-related gene pairs (IRGP) signature to evaluate the prognosis of EC. RESULTS: The IRGP signature was trained by the TCGA cohort and validated by three GEO datasets, respectively. Cox regression model together with LASSO was applied to construct the overall survival (OS) associated IRGP. 21 IRGPs consisting of 38 immune-related genes were included in our signature, according to which patients were stratified into high- and low-risk groups. The results of Kaplan-Meier survival analyses indicated that high-risk EC patients had worse OS than low-risk group in the training set, meta-validation set and all independent validation datasets. After adjustment in multivariate Cox analyses, our signature continued to be an independent prognostic factor of EC and the signature-based nomogram could effectively predict the prognosis of EC sufferers. Besides, Gene Ontology analysis revealed this signature is related to immunity. ‘CIBERSORT’ analysis revealed the infiltration levels of plasma cells and activated CD4 memory T cells in two risk groups were significantly different. Ultimately, we validated the expression levels of six selected genes from IRGP index in KYSE-150 and KYSE-450. CONCLUSIONS: This IRGP signature could be applied to select EC patients with high mortality risk, thereby improving prospects for the treatment of EC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09496-x. |
format | Online Article Text |
id | pubmed-10332031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103320312023-07-11 A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer Zheng, Wei Fang, Gaofeng Huang, Qiao Shi, Dan Xie, Biao BMC Genomics Research BACKGROUND: Identifying reliable biomarkers could effectively predict esophagus carcinoma (EC) patients with poor prognosis. In this work, we constructed an immune-related gene pairs (IRGP) signature to evaluate the prognosis of EC. RESULTS: The IRGP signature was trained by the TCGA cohort and validated by three GEO datasets, respectively. Cox regression model together with LASSO was applied to construct the overall survival (OS) associated IRGP. 21 IRGPs consisting of 38 immune-related genes were included in our signature, according to which patients were stratified into high- and low-risk groups. The results of Kaplan-Meier survival analyses indicated that high-risk EC patients had worse OS than low-risk group in the training set, meta-validation set and all independent validation datasets. After adjustment in multivariate Cox analyses, our signature continued to be an independent prognostic factor of EC and the signature-based nomogram could effectively predict the prognosis of EC sufferers. Besides, Gene Ontology analysis revealed this signature is related to immunity. ‘CIBERSORT’ analysis revealed the infiltration levels of plasma cells and activated CD4 memory T cells in two risk groups were significantly different. Ultimately, we validated the expression levels of six selected genes from IRGP index in KYSE-150 and KYSE-450. CONCLUSIONS: This IRGP signature could be applied to select EC patients with high mortality risk, thereby improving prospects for the treatment of EC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09496-x. BioMed Central 2023-07-10 /pmc/articles/PMC10332031/ /pubmed/37430202 http://dx.doi.org/10.1186/s12864-023-09496-x Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zheng, Wei Fang, Gaofeng Huang, Qiao Shi, Dan Xie, Biao A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
title | A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
title_full | A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
title_fullStr | A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
title_full_unstemmed | A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
title_short | A robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
title_sort | robust immune-related gene pairs signature for predicting the overall survival of esophageal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332031/ https://www.ncbi.nlm.nih.gov/pubmed/37430202 http://dx.doi.org/10.1186/s12864-023-09496-x |
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