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A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma
Aberrant immunity has been associated with the initiation and progression of cancers such as hepatocellular carcinoma (HCC). Here, we aim to develop a signature based on immune-related genes (IRGs) to predict the prognosis of HCC patients. The gene expression profiles of 891 HCC samples were derived...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376334/ https://www.ncbi.nlm.nih.gov/pubmed/34414957 http://dx.doi.org/10.1097/MD.0000000000026948 |
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author | Li, Qinghe Fan, Bin Ding, Jun Xiang, Xiaoxi Zhang, Jian |
author_facet | Li, Qinghe Fan, Bin Ding, Jun Xiang, Xiaoxi Zhang, Jian |
author_sort | Li, Qinghe |
collection | PubMed |
description | Aberrant immunity has been associated with the initiation and progression of cancers such as hepatocellular carcinoma (HCC). Here, we aim to develop a signature based on immune-related genes (IRGs) to predict the prognosis of HCC patients. The gene expression profiles of 891 HCC samples were derived from 4 publicly accessible datasets. A total of 1534 IRGs from Immunology Database and Analysis Portal website were obtained as candidate genes for prognostic assessment. Using least absolute shrinkage and selection operator (LASSO) regression analysis, 12 IRGs were selected as prognostic biomarkers and were then aggregated to generate an IRG score for each HCC sample. In the training dataset (n = 365), patients with high IRG scores showed a remarkably poorer overall survival than those with low IRG scores (log-rank P < .001). Similar results were documented in 3 independent testing datasets (n = 226, 221, 79, respectively). Multivariate Cox regression and stratified analyses indicated that the IRG score was an independent and robust signature to predict the overall survival in HCC patients. Patients with high IRG scores tended to be in advanced TNM stages, with increased risks of tumor recurrence and metastasis. More importantly, the IRG score was strongly associated with certain immune cell counts, gene expression of immune checkpoints, estimated immune score, and mutation of critical genes in HCC. In conclusion, the proposed IRG score can predict the prognosis and reflect the tumor immune microenvironment of HCC patients, which may facilitate the individualized treatment and provide potential immunotherapeutic targets. |
format | Online Article Text |
id | pubmed-8376334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-83763342021-08-21 A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma Li, Qinghe Fan, Bin Ding, Jun Xiang, Xiaoxi Zhang, Jian Medicine (Baltimore) 4500 Aberrant immunity has been associated with the initiation and progression of cancers such as hepatocellular carcinoma (HCC). Here, we aim to develop a signature based on immune-related genes (IRGs) to predict the prognosis of HCC patients. The gene expression profiles of 891 HCC samples were derived from 4 publicly accessible datasets. A total of 1534 IRGs from Immunology Database and Analysis Portal website were obtained as candidate genes for prognostic assessment. Using least absolute shrinkage and selection operator (LASSO) regression analysis, 12 IRGs were selected as prognostic biomarkers and were then aggregated to generate an IRG score for each HCC sample. In the training dataset (n = 365), patients with high IRG scores showed a remarkably poorer overall survival than those with low IRG scores (log-rank P < .001). Similar results were documented in 3 independent testing datasets (n = 226, 221, 79, respectively). Multivariate Cox regression and stratified analyses indicated that the IRG score was an independent and robust signature to predict the overall survival in HCC patients. Patients with high IRG scores tended to be in advanced TNM stages, with increased risks of tumor recurrence and metastasis. More importantly, the IRG score was strongly associated with certain immune cell counts, gene expression of immune checkpoints, estimated immune score, and mutation of critical genes in HCC. In conclusion, the proposed IRG score can predict the prognosis and reflect the tumor immune microenvironment of HCC patients, which may facilitate the individualized treatment and provide potential immunotherapeutic targets. Lippincott Williams & Wilkins 2021-08-20 /pmc/articles/PMC8376334/ /pubmed/34414957 http://dx.doi.org/10.1097/MD.0000000000026948 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 4500 Li, Qinghe Fan, Bin Ding, Jun Xiang, Xiaoxi Zhang, Jian A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
title | A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
title_full | A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
title_fullStr | A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
title_full_unstemmed | A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
title_short | A novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
title_sort | novel immune signature to predict the prognosis of patients with hepatocellular carcinoma |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376334/ https://www.ncbi.nlm.nih.gov/pubmed/34414957 http://dx.doi.org/10.1097/MD.0000000000026948 |
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