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Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients

OBJECTIVE: In this research, we studied the genes associated with ferroptosis to develop a prognostic model and find out an association with tumor immune microenvironment in skin cutaneous melanoma (SKCM) patients. METHODS: To find SKCM-related ferroptosis genes, we used Cox regression and LASSO app...

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Autores principales: Zeng, Ni, Ma, Liwen, Cheng, Yuxin, Xia, Qingyue, Li, Yueyue, Chen, Yihe, Lu, Zhiyu, Lu, Qian, Jiang, Feng, Luo, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502037/
https://www.ncbi.nlm.nih.gov/pubmed/34675611
http://dx.doi.org/10.2147/IJGM.S327348
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author Zeng, Ni
Ma, Liwen
Cheng, Yuxin
Xia, Qingyue
Li, Yueyue
Chen, Yihe
Lu, Zhiyu
Lu, Qian
Jiang, Feng
Luo, Dan
author_facet Zeng, Ni
Ma, Liwen
Cheng, Yuxin
Xia, Qingyue
Li, Yueyue
Chen, Yihe
Lu, Zhiyu
Lu, Qian
Jiang, Feng
Luo, Dan
author_sort Zeng, Ni
collection PubMed
description OBJECTIVE: In this research, we studied the genes associated with ferroptosis to develop a prognostic model and find out an association with tumor immune microenvironment in skin cutaneous melanoma (SKCM) patients. METHODS: To find SKCM-related ferroptosis genes, we used Cox regression and LASSO approach on 60 genes related to ferroptosis and SKCM-related RNA-seq. Following that, a ferroptosis-related gene signature was created. Time-dependent ROC curve and Kaplan–Meier analysis were calculated to determine its capability of prediction. Besides, several assessments were used to evaluate overall survival (OS), accompanied by the creation of a nomogram for the clinicopathologic factors and the ferroptosis-related gene signature we established. We also investigated the relationship between ferroptosis-related gene signature with three immune checkpoints and immune cell infiltration. RESULTS: Our prognostic model included two genes (ALOX5, CHAC1). In both TCGA and GEO cohorts, OS was lower in high-risk category. Using our gene signature, we can reliably predict OS. Additionally, our gene signature can predict immune cell infiltration and SKCM immunotherapy response. CONCLUSION: Our gene signature has shown to be a reliable predictor of OS, reflect the immune microenvironment, and predict the effectiveness of immunotherapy for SKCM patients.
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spelling pubmed-85020372021-10-20 Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients Zeng, Ni Ma, Liwen Cheng, Yuxin Xia, Qingyue Li, Yueyue Chen, Yihe Lu, Zhiyu Lu, Qian Jiang, Feng Luo, Dan Int J Gen Med Original Research OBJECTIVE: In this research, we studied the genes associated with ferroptosis to develop a prognostic model and find out an association with tumor immune microenvironment in skin cutaneous melanoma (SKCM) patients. METHODS: To find SKCM-related ferroptosis genes, we used Cox regression and LASSO approach on 60 genes related to ferroptosis and SKCM-related RNA-seq. Following that, a ferroptosis-related gene signature was created. Time-dependent ROC curve and Kaplan–Meier analysis were calculated to determine its capability of prediction. Besides, several assessments were used to evaluate overall survival (OS), accompanied by the creation of a nomogram for the clinicopathologic factors and the ferroptosis-related gene signature we established. We also investigated the relationship between ferroptosis-related gene signature with three immune checkpoints and immune cell infiltration. RESULTS: Our prognostic model included two genes (ALOX5, CHAC1). In both TCGA and GEO cohorts, OS was lower in high-risk category. Using our gene signature, we can reliably predict OS. Additionally, our gene signature can predict immune cell infiltration and SKCM immunotherapy response. CONCLUSION: Our gene signature has shown to be a reliable predictor of OS, reflect the immune microenvironment, and predict the effectiveness of immunotherapy for SKCM patients. Dove 2021-10-05 /pmc/articles/PMC8502037/ /pubmed/34675611 http://dx.doi.org/10.2147/IJGM.S327348 Text en © 2021 Zeng et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zeng, Ni
Ma, Liwen
Cheng, Yuxin
Xia, Qingyue
Li, Yueyue
Chen, Yihe
Lu, Zhiyu
Lu, Qian
Jiang, Feng
Luo, Dan
Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients
title Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients
title_full Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients
title_fullStr Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients
title_full_unstemmed Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients
title_short Construction of a Ferroptosis-Related Gene Signature for Predicting Survival and Immune Microenvironment in Melanoma Patients
title_sort construction of a ferroptosis-related gene signature for predicting survival and immune microenvironment in melanoma patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502037/
https://www.ncbi.nlm.nih.gov/pubmed/34675611
http://dx.doi.org/10.2147/IJGM.S327348
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