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Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer

Gastric cancer is one of the most common malignancies. Although some patients benefit from immunotherapy, the majority of patients have unsatisfactory immunotherapy outcomes, and the clinical significance of immune-related genes in gastric cancer remains unknown. We used the single-sample gene set e...

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Autores principales: Ning, Jingyuan, Sun, Keran, Fan, Xiaoqing, Jia, Keqi, Meng, Lingtong, Wang, Xiuli, Li, Hui, Ma, Ruixiao, Liu, Subin, Li, Feng, Wang, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148812/
https://www.ncbi.nlm.nih.gov/pubmed/37120631
http://dx.doi.org/10.1038/s41598-023-34291-9
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author Ning, Jingyuan
Sun, Keran
Fan, Xiaoqing
Jia, Keqi
Meng, Lingtong
Wang, Xiuli
Li, Hui
Ma, Ruixiao
Liu, Subin
Li, Feng
Wang, Xiaofeng
author_facet Ning, Jingyuan
Sun, Keran
Fan, Xiaoqing
Jia, Keqi
Meng, Lingtong
Wang, Xiuli
Li, Hui
Ma, Ruixiao
Liu, Subin
Li, Feng
Wang, Xiaofeng
author_sort Ning, Jingyuan
collection PubMed
description Gastric cancer is one of the most common malignancies. Although some patients benefit from immunotherapy, the majority of patients have unsatisfactory immunotherapy outcomes, and the clinical significance of immune-related genes in gastric cancer remains unknown. We used the single-sample gene set enrichment analysis (ssGSEA) method to evaluate the immune cell content of gastric cancer patients from TCGA and clustered patients based on immune cell scores. The Weighted Correlation Network Analysis (WGCNA) algorithm was used to identify immune subtype-related genes. The patients in TCGA were randomly divided into test 1 and test 2 in a 1:1 ratio, and a machine learning integration process was used to determine the best prognostic signatures in the total cohort. The signatures were then validated in the test 1 and the test 2 cohort. Based on a literature search, we selected 93 previously published prognostic signatures for gastric cancer and compared them with our prognostic signatures. At the single-cell level, the algorithms "Seurat," "SCEVAN", "scissor", and "Cellchat" were used to demonstrate the cell communication disturbance of high-risk cells. WGCNA and univariate Cox regression analysis identified 52 prognosis-related genes, which were subjected to 98 machine-learning integration processes. A prognostic signature consisting of 24 genes was identified using the StepCox[backward] and Enet[alpha = 0.7] machine learning algorithms. This signature demonstrated the best prognostic performance in the overall, test1 and test2 cohort, and outperformed 93 previously published prognostic signatures. Interaction perturbations in cellular communication of high-risk T cells were identified at the single-cell level, which may promote disease progression in patients with gastric cancer. We developed an immune-related prognostic signature with reliable validity and high accuracy for clinical use for predicting the prognosis of patients with gastric cancer.
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spelling pubmed-101488122023-05-01 Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer Ning, Jingyuan Sun, Keran Fan, Xiaoqing Jia, Keqi Meng, Lingtong Wang, Xiuli Li, Hui Ma, Ruixiao Liu, Subin Li, Feng Wang, Xiaofeng Sci Rep Article Gastric cancer is one of the most common malignancies. Although some patients benefit from immunotherapy, the majority of patients have unsatisfactory immunotherapy outcomes, and the clinical significance of immune-related genes in gastric cancer remains unknown. We used the single-sample gene set enrichment analysis (ssGSEA) method to evaluate the immune cell content of gastric cancer patients from TCGA and clustered patients based on immune cell scores. The Weighted Correlation Network Analysis (WGCNA) algorithm was used to identify immune subtype-related genes. The patients in TCGA were randomly divided into test 1 and test 2 in a 1:1 ratio, and a machine learning integration process was used to determine the best prognostic signatures in the total cohort. The signatures were then validated in the test 1 and the test 2 cohort. Based on a literature search, we selected 93 previously published prognostic signatures for gastric cancer and compared them with our prognostic signatures. At the single-cell level, the algorithms "Seurat," "SCEVAN", "scissor", and "Cellchat" were used to demonstrate the cell communication disturbance of high-risk cells. WGCNA and univariate Cox regression analysis identified 52 prognosis-related genes, which were subjected to 98 machine-learning integration processes. A prognostic signature consisting of 24 genes was identified using the StepCox[backward] and Enet[alpha = 0.7] machine learning algorithms. This signature demonstrated the best prognostic performance in the overall, test1 and test2 cohort, and outperformed 93 previously published prognostic signatures. Interaction perturbations in cellular communication of high-risk T cells were identified at the single-cell level, which may promote disease progression in patients with gastric cancer. We developed an immune-related prognostic signature with reliable validity and high accuracy for clinical use for predicting the prognosis of patients with gastric cancer. Nature Publishing Group UK 2023-04-29 /pmc/articles/PMC10148812/ /pubmed/37120631 http://dx.doi.org/10.1038/s41598-023-34291-9 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/) .
spellingShingle Article
Ning, Jingyuan
Sun, Keran
Fan, Xiaoqing
Jia, Keqi
Meng, Lingtong
Wang, Xiuli
Li, Hui
Ma, Ruixiao
Liu, Subin
Li, Feng
Wang, Xiaofeng
Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
title Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
title_full Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
title_fullStr Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
title_full_unstemmed Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
title_short Use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
title_sort use of machine learning-based integration to develop an immune-related signature for improving prognosis in patients with gastric cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148812/
https://www.ncbi.nlm.nih.gov/pubmed/37120631
http://dx.doi.org/10.1038/s41598-023-34291-9
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