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A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma
Osteosarcoma (OS) is the most common bone cancer in adolescents, and has a high propensity to metastasize. Ferroptosis is a unique modality of cell death, driving the metastasis of cancer cells. Identifying ferroptosis-related genes (FRGs) as prognostic factors will be critical to predict the outcom...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771194/ https://www.ncbi.nlm.nih.gov/pubmed/36550843 http://dx.doi.org/10.1097/MD.0000000000032083 |
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author | Ge, Zhanyong Song, Delei |
author_facet | Ge, Zhanyong Song, Delei |
author_sort | Ge, Zhanyong |
collection | PubMed |
description | Osteosarcoma (OS) is the most common bone cancer in adolescents, and has a high propensity to metastasize. Ferroptosis is a unique modality of cell death, driving the metastasis of cancer cells. Identifying ferroptosis-related genes (FRGs) as prognostic factors will be critical to predict the outcomes of OS. This study aimed to explore the prognostic value of FRGs in OS and build a prognostic model to indirectly improve OS patients’ outcomes. METHODS: OS data were downloaded from the TARGET database and 2 Gene Expression Omnibus datasets. Univariate Cox regression was conducted to assess FRGs. A risk score model basing on 5 FRGs was constructed via LASSO-Cox regression. Multivariate Cox regression analysis was used to determine the independent prognostic factors. The Nomogram model was built using independent prognostic factors. The relationship between the risk score and the immune cell infiltration was estimated by CIBERSORT, and the correlation between the risk score and immune checkpoints was also analyzed. RESULTS: Based on the prognosis-related FRGs, we built a regression model: Risk score = (−0.01382853 × ACSL4) − (0.05371778 × HMOX1) − (0.02434655 × GPX4) − (0.16432810 × PRNP) − (0.15567120 × ATG7). OS patients with high risk score tended to suffer from poor prognosis, validated in 2 Gene Expression Omnibus datasets. The Nomogram model showed the combination of the risk score and the tumour-node-metastasis stage improved predictive effectiveness. The risk score was also related to immune cell infiltration and immune checkpoint expression. CONCLUSION: The risk score model based on 5 FRGs was a reliable prognostic predictive indicator for OS patients. |
format | Online Article Text |
id | pubmed-9771194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-97711942022-12-22 A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma Ge, Zhanyong Song, Delei Medicine (Baltimore) 5700 Osteosarcoma (OS) is the most common bone cancer in adolescents, and has a high propensity to metastasize. Ferroptosis is a unique modality of cell death, driving the metastasis of cancer cells. Identifying ferroptosis-related genes (FRGs) as prognostic factors will be critical to predict the outcomes of OS. This study aimed to explore the prognostic value of FRGs in OS and build a prognostic model to indirectly improve OS patients’ outcomes. METHODS: OS data were downloaded from the TARGET database and 2 Gene Expression Omnibus datasets. Univariate Cox regression was conducted to assess FRGs. A risk score model basing on 5 FRGs was constructed via LASSO-Cox regression. Multivariate Cox regression analysis was used to determine the independent prognostic factors. The Nomogram model was built using independent prognostic factors. The relationship between the risk score and the immune cell infiltration was estimated by CIBERSORT, and the correlation between the risk score and immune checkpoints was also analyzed. RESULTS: Based on the prognosis-related FRGs, we built a regression model: Risk score = (−0.01382853 × ACSL4) − (0.05371778 × HMOX1) − (0.02434655 × GPX4) − (0.16432810 × PRNP) − (0.15567120 × ATG7). OS patients with high risk score tended to suffer from poor prognosis, validated in 2 Gene Expression Omnibus datasets. The Nomogram model showed the combination of the risk score and the tumour-node-metastasis stage improved predictive effectiveness. The risk score was also related to immune cell infiltration and immune checkpoint expression. CONCLUSION: The risk score model based on 5 FRGs was a reliable prognostic predictive indicator for OS patients. Lippincott Williams & Wilkins 2022-12-16 /pmc/articles/PMC9771194/ /pubmed/36550843 http://dx.doi.org/10.1097/MD.0000000000032083 Text en Copyright © 2022 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) (https://creativecommons.org/licenses/by-nc/4.0/) , 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. |
spellingShingle | 5700 Ge, Zhanyong Song, Delei A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
title | A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
title_full | A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
title_fullStr | A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
title_full_unstemmed | A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
title_short | A five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
title_sort | five ferroptosis-related genes risk score for prognostic prediction of osteosarcoma |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771194/ https://www.ncbi.nlm.nih.gov/pubmed/36550843 http://dx.doi.org/10.1097/MD.0000000000032083 |
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