Cargando…
Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction
BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignant cancers, and few studies have demonstrated the value of ferroptosis-related genes in prognosis. METHODS: The original counts of RNA sequencing data and clinicopathological data were obtained from TCGA and G...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711242/ https://www.ncbi.nlm.nih.gov/pubmed/34992433 http://dx.doi.org/10.2147/IJGM.S343233 |
_version_ | 1784623331205447680 |
---|---|
author | Li, Qun Jin, Yangli Shen, Zhisen Liu, Huigao Shen, Yi Wu, Zhenhua |
author_facet | Li, Qun Jin, Yangli Shen, Zhisen Liu, Huigao Shen, Yi Wu, Zhenhua |
author_sort | Li, Qun |
collection | PubMed |
description | BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignant cancers, and few studies have demonstrated the value of ferroptosis-related genes in prognosis. METHODS: The original counts of RNA sequencing data and clinicopathological data were obtained from TCGA and GSE65858 datasets. Common ferroptosis-related genes related to prognosis were identified from the training set and were included in LASSO to determine the best prognosis. To evaluate the efficacy, time-dependent ROC and Kaplan–Meier (KM) survival analyses were applied. Moreover, univariate and multivariate Cox regression analyses were used to screen independent parameters of prognosis and build a nomogram. Eventually, possible biological pathways were proposed based on GSEA. RESULTS: Among 242 ferroptosis-related genes, we identified that the FLT3, IL6, Keap1, NQO1, SOCS1 and TRIB3 genes were significantly connected with HNSCC patient prognosis as a six-gene signature. After, the patients were divided into high- and low-risk groups based on the six-gene signature. The KM survival curves demonstrated that the high-risk group had worse OS (p < 0.0001) and higher AUC values (0.654, 0.735, and 0.679 for 1-, 3-, and 5-year survival, respectively) for the prognostic signature of the six genes compared with other genes, which were also validated in the GSE65858 dataset. Moreover, GSEA suggested that the epithelial mesenchymal transition pathway was abundant and that the mesenchymal status in the high-risk group was substantially higher than that in the low-risk group. Finally, the immune microenvironment and differences in the content of immune cell types were demonstrated. CONCLUSION: We established a six-ferroptosis-related-gene model crossing clinical prognostic parameters that can predict HNSCC patient prognosis and provide a reliable prognostic evaluation tool to assist clinical treatment decisions. |
format | Online Article Text |
id | pubmed-8711242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-87112422022-01-05 Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction Li, Qun Jin, Yangli Shen, Zhisen Liu, Huigao Shen, Yi Wu, Zhenhua Int J Gen Med Original Research BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignant cancers, and few studies have demonstrated the value of ferroptosis-related genes in prognosis. METHODS: The original counts of RNA sequencing data and clinicopathological data were obtained from TCGA and GSE65858 datasets. Common ferroptosis-related genes related to prognosis were identified from the training set and were included in LASSO to determine the best prognosis. To evaluate the efficacy, time-dependent ROC and Kaplan–Meier (KM) survival analyses were applied. Moreover, univariate and multivariate Cox regression analyses were used to screen independent parameters of prognosis and build a nomogram. Eventually, possible biological pathways were proposed based on GSEA. RESULTS: Among 242 ferroptosis-related genes, we identified that the FLT3, IL6, Keap1, NQO1, SOCS1 and TRIB3 genes were significantly connected with HNSCC patient prognosis as a six-gene signature. After, the patients were divided into high- and low-risk groups based on the six-gene signature. The KM survival curves demonstrated that the high-risk group had worse OS (p < 0.0001) and higher AUC values (0.654, 0.735, and 0.679 for 1-, 3-, and 5-year survival, respectively) for the prognostic signature of the six genes compared with other genes, which were also validated in the GSE65858 dataset. Moreover, GSEA suggested that the epithelial mesenchymal transition pathway was abundant and that the mesenchymal status in the high-risk group was substantially higher than that in the low-risk group. Finally, the immune microenvironment and differences in the content of immune cell types were demonstrated. CONCLUSION: We established a six-ferroptosis-related-gene model crossing clinical prognostic parameters that can predict HNSCC patient prognosis and provide a reliable prognostic evaluation tool to assist clinical treatment decisions. Dove 2021-12-21 /pmc/articles/PMC8711242/ /pubmed/34992433 http://dx.doi.org/10.2147/IJGM.S343233 Text en © 2021 Li 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 Li, Qun Jin, Yangli Shen, Zhisen Liu, Huigao Shen, Yi Wu, Zhenhua Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction |
title | Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction |
title_full | Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction |
title_fullStr | Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction |
title_full_unstemmed | Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction |
title_short | Construction of a Ferroptosis-Related Gene Signature for Head and Neck Squamous Cell Carcinoma Prognosis Prediction |
title_sort | construction of a ferroptosis-related gene signature for head and neck squamous cell carcinoma prognosis prediction |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711242/ https://www.ncbi.nlm.nih.gov/pubmed/34992433 http://dx.doi.org/10.2147/IJGM.S343233 |
work_keys_str_mv | AT liqun constructionofaferroptosisrelatedgenesignatureforheadandnecksquamouscellcarcinomaprognosisprediction AT jinyangli constructionofaferroptosisrelatedgenesignatureforheadandnecksquamouscellcarcinomaprognosisprediction AT shenzhisen constructionofaferroptosisrelatedgenesignatureforheadandnecksquamouscellcarcinomaprognosisprediction AT liuhuigao constructionofaferroptosisrelatedgenesignatureforheadandnecksquamouscellcarcinomaprognosisprediction AT shenyi constructionofaferroptosisrelatedgenesignatureforheadandnecksquamouscellcarcinomaprognosisprediction AT wuzhenhua constructionofaferroptosisrelatedgenesignatureforheadandnecksquamouscellcarcinomaprognosisprediction |