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Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma

BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. A novel form of copper-dependent and reactive oxygen species (ROS)-dependent cell death, cuproptosis, has been described in many cancers. The roles and potential mechanisms of cuproptosis-related gen...

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Autores principales: Wang, Chi, Zhou, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496405/
https://www.ncbi.nlm.nih.gov/pubmed/37697421
http://dx.doi.org/10.1186/s40463-023-00655-4
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author Wang, Chi
Zhou, Yu
author_facet Wang, Chi
Zhou, Yu
author_sort Wang, Chi
collection PubMed
description BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. A novel form of copper-dependent and reactive oxygen species (ROS)-dependent cell death, cuproptosis, has been described in many cancers. The roles and potential mechanisms of cuproptosis-related genes (CRGs) are still unclear in HNSCC. METHOD: We downloaded TCGA datasets of HNSCC genomic mutations and clinic data from The Cancer Genome Atlas. Based on the Cuproptosis-related differentially expressed genes in HNSCC, we constructed a prognostic signature. RESULTS: Eight CRGs have been identified as associated with the prognosis of HNSCC. According to Kaplan–Meier analyses, HNSCC with a high Risk Score had a poor prognosis. Furthermore, the AUC of the Risk Score for the 1-, 3-, and 5- year overall survival was respectively, 0.70, 0.71, and 0.68. TCGA data revealed that T cell functions, such as HLA, cytolytic activity, inflammation regulation, co-inhibition, and co-stimulation, differed significantly between members of the low and high groups. The immune checkpoint genes PD-L1, PD-L1, and CTLA-4 were also expressed differently in the two risk groups. CONCLUSIONS: A CRG signature was defined that is associated with the prognosis of patients with HNSCC. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40463-023-00655-4.
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spelling pubmed-104964052023-09-13 Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma Wang, Chi Zhou, Yu J Otolaryngol Head Neck Surg Original Research Article BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. A novel form of copper-dependent and reactive oxygen species (ROS)-dependent cell death, cuproptosis, has been described in many cancers. The roles and potential mechanisms of cuproptosis-related genes (CRGs) are still unclear in HNSCC. METHOD: We downloaded TCGA datasets of HNSCC genomic mutations and clinic data from The Cancer Genome Atlas. Based on the Cuproptosis-related differentially expressed genes in HNSCC, we constructed a prognostic signature. RESULTS: Eight CRGs have been identified as associated with the prognosis of HNSCC. According to Kaplan–Meier analyses, HNSCC with a high Risk Score had a poor prognosis. Furthermore, the AUC of the Risk Score for the 1-, 3-, and 5- year overall survival was respectively, 0.70, 0.71, and 0.68. TCGA data revealed that T cell functions, such as HLA, cytolytic activity, inflammation regulation, co-inhibition, and co-stimulation, differed significantly between members of the low and high groups. The immune checkpoint genes PD-L1, PD-L1, and CTLA-4 were also expressed differently in the two risk groups. CONCLUSIONS: A CRG signature was defined that is associated with the prognosis of patients with HNSCC. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40463-023-00655-4. BioMed Central 2023-09-12 /pmc/articles/PMC10496405/ /pubmed/37697421 http://dx.doi.org/10.1186/s40463-023-00655-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Original Research Article
Wang, Chi
Zhou, Yu
Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
title Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
title_full Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
title_fullStr Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
title_full_unstemmed Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
title_short Cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
title_sort cuproptosis-related gene subtypes predict prognosis in patients with head and neck squamous cell carcinoma
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496405/
https://www.ncbi.nlm.nih.gov/pubmed/37697421
http://dx.doi.org/10.1186/s40463-023-00655-4
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