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Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma
Ferroptosis is a novel type of iron- and ROS-dependent cell death and is involved in various diseases. LncRNAs are involved and play important roles in the occurrence and development of several cancers. However, researches about the role of ferroptosis-related lncRNAs in glioma are relatively rare....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842255/ https://www.ncbi.nlm.nih.gov/pubmed/35174152 http://dx.doi.org/10.3389/fcell.2022.817643 |
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author | Shi, Junfeng Lai, Donglin Zuo, Xiaojia Liu, Dingsheng Chen, Bing Zheng, Yanjun Lu, Changlian Gu, Xuefeng |
author_facet | Shi, Junfeng Lai, Donglin Zuo, Xiaojia Liu, Dingsheng Chen, Bing Zheng, Yanjun Lu, Changlian Gu, Xuefeng |
author_sort | Shi, Junfeng |
collection | PubMed |
description | Ferroptosis is a novel type of iron- and ROS-dependent cell death and is involved in various diseases. LncRNAs are involved and play important roles in the occurrence and development of several cancers. However, researches about the role of ferroptosis-related lncRNAs in glioma are relatively rare. Here, we identified nine ferroptosis-related lncRNAs and then constructed a prognostic model by the LASSO and Cox analysis. The model could predict overall survival with high sensitivity and specificity according to ROC curves. In addition, the cell cycle, p53 signaling, apoptosis, and oxidative phosphorylation pathways were obviously enriched in the pathogenesis of glioma by gene set enrichment analysis. A nomogram was constructed by integrating several independent prognostic clinicopathological features, and it could provide a valuable predictive tool for overall survival. Furthermore, a strong correlation between these nine lncRNAs and immunotherapy was found. Glioma patients in the high-risk group had higher TMB using somatic mutation data, different immune infiltration, and higher expression of immune checkpoints, indicating these patients might benefit from immune checkpoint inhibitor therapy. In summary, these nine ferroptosis-related lncRNAs were promising biomarkers for predicting overall survival and guiding immunotherapy or future immune checkpoint inhibitor development for glioma patients. |
format | Online Article Text |
id | pubmed-8842255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88422552022-02-15 Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma Shi, Junfeng Lai, Donglin Zuo, Xiaojia Liu, Dingsheng Chen, Bing Zheng, Yanjun Lu, Changlian Gu, Xuefeng Front Cell Dev Biol Cell and Developmental Biology Ferroptosis is a novel type of iron- and ROS-dependent cell death and is involved in various diseases. LncRNAs are involved and play important roles in the occurrence and development of several cancers. However, researches about the role of ferroptosis-related lncRNAs in glioma are relatively rare. Here, we identified nine ferroptosis-related lncRNAs and then constructed a prognostic model by the LASSO and Cox analysis. The model could predict overall survival with high sensitivity and specificity according to ROC curves. In addition, the cell cycle, p53 signaling, apoptosis, and oxidative phosphorylation pathways were obviously enriched in the pathogenesis of glioma by gene set enrichment analysis. A nomogram was constructed by integrating several independent prognostic clinicopathological features, and it could provide a valuable predictive tool for overall survival. Furthermore, a strong correlation between these nine lncRNAs and immunotherapy was found. Glioma patients in the high-risk group had higher TMB using somatic mutation data, different immune infiltration, and higher expression of immune checkpoints, indicating these patients might benefit from immune checkpoint inhibitor therapy. In summary, these nine ferroptosis-related lncRNAs were promising biomarkers for predicting overall survival and guiding immunotherapy or future immune checkpoint inhibitor development for glioma patients. Frontiers Media S.A. 2022-01-31 /pmc/articles/PMC8842255/ /pubmed/35174152 http://dx.doi.org/10.3389/fcell.2022.817643 Text en Copyright © 2022 Shi, Lai, Zuo, Liu, Chen, Zheng, Lu and Gu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Shi, Junfeng Lai, Donglin Zuo, Xiaojia Liu, Dingsheng Chen, Bing Zheng, Yanjun Lu, Changlian Gu, Xuefeng Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma |
title | Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma |
title_full | Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma |
title_fullStr | Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma |
title_full_unstemmed | Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma |
title_short | Identification of Ferroptosis-Related Biomarkers for Prognosis and Immunotherapy in Patients With Glioma |
title_sort | identification of ferroptosis-related biomarkers for prognosis and immunotherapy in patients with glioma |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842255/ https://www.ncbi.nlm.nih.gov/pubmed/35174152 http://dx.doi.org/10.3389/fcell.2022.817643 |
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