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Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types

BACKGROUND: The COP9 signalosome subunit 6 (COPS6) has been implicated in cancer progression, while its precise role in most types of cancer remains elusive. AIM: To investigate the functional and clinical relevance of COPS6 across various tumor types using publicly available databases. METHODS: We...

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Autores principales: Wang, Shi-Lin, Zhuo, Guang-Zheng, Wang, Li-Ping, Jiang, Xiang-Hu, Liu, Guo-Hong, Pan, Yun-Bao, Li, Yi-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696221/
http://dx.doi.org/10.5306/wjco.v14.i11.479
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author Wang, Shi-Lin
Zhuo, Guang-Zheng
Wang, Li-Ping
Jiang, Xiang-Hu
Liu, Guo-Hong
Pan, Yun-Bao
Li, Yi-Rong
author_facet Wang, Shi-Lin
Zhuo, Guang-Zheng
Wang, Li-Ping
Jiang, Xiang-Hu
Liu, Guo-Hong
Pan, Yun-Bao
Li, Yi-Rong
author_sort Wang, Shi-Lin
collection PubMed
description BACKGROUND: The COP9 signalosome subunit 6 (COPS6) has been implicated in cancer progression, while its precise role in most types of cancer remains elusive. AIM: To investigate the functional and clinical relevance of COPS6 across various tumor types using publicly available databases. METHODS: We used R software and online analysis databases to analyze the differential expression, prognosis, mutation and related functions of COPS6 in pan-cancer. RESULTS: Differential expression analysis and survival analysis demonstrated that COPS6 was highly expressed and associated with high-risk profiles in the majority of cancer types. Possible associations between COPS6 expression level and prognostic outcomes were found using data from public databases. Mutational analysis revealed that missense mutations were the predominant type of COPS6 mutation. Additionally, positive correlations were identified between COPS6 expression level and tumor mutational burden and microsatellite instability in most types of cancer. Immune infiltration analysis demonstrated a negative correlation between COPS6 expression level and CD8+ T cell infiltration in certain types of cancer. The correlation between COPS6 expression level and cancer-associated fibroblast infiltration exhibited heterogeneity, in which a positive correlation was found in head and neck squamous cell carcinoma and tenosynovial giant cell tumor, and a negative correlation was identified in diffuse large B-cell lymphoma and thymoma. The correlation between COPS6 expression level and macrophage infiltration was closely related to macrophage type. Gene co-expression and enrichment analysis highlighted transcription elongation factor B polypeptide 2 and G protein pathway suppressor 1 were significantly and positively associated with COPS6 expression level. These genes were predominantly involved in processes, such as ubiquitin-mediated proteolysis and human immunodeficiency virus 1 infection. CONCLUSION: In conclusion, this study systematically explored the significance of COPS6 across different tumor types, providing a solid foundation for considering COPS6 as a novel biomarker in cancer research.
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spelling pubmed-106962212023-12-06 Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types Wang, Shi-Lin Zhuo, Guang-Zheng Wang, Li-Ping Jiang, Xiang-Hu Liu, Guo-Hong Pan, Yun-Bao Li, Yi-Rong World J Clin Oncol Basic Study BACKGROUND: The COP9 signalosome subunit 6 (COPS6) has been implicated in cancer progression, while its precise role in most types of cancer remains elusive. AIM: To investigate the functional and clinical relevance of COPS6 across various tumor types using publicly available databases. METHODS: We used R software and online analysis databases to analyze the differential expression, prognosis, mutation and related functions of COPS6 in pan-cancer. RESULTS: Differential expression analysis and survival analysis demonstrated that COPS6 was highly expressed and associated with high-risk profiles in the majority of cancer types. Possible associations between COPS6 expression level and prognostic outcomes were found using data from public databases. Mutational analysis revealed that missense mutations were the predominant type of COPS6 mutation. Additionally, positive correlations were identified between COPS6 expression level and tumor mutational burden and microsatellite instability in most types of cancer. Immune infiltration analysis demonstrated a negative correlation between COPS6 expression level and CD8+ T cell infiltration in certain types of cancer. The correlation between COPS6 expression level and cancer-associated fibroblast infiltration exhibited heterogeneity, in which a positive correlation was found in head and neck squamous cell carcinoma and tenosynovial giant cell tumor, and a negative correlation was identified in diffuse large B-cell lymphoma and thymoma. The correlation between COPS6 expression level and macrophage infiltration was closely related to macrophage type. Gene co-expression and enrichment analysis highlighted transcription elongation factor B polypeptide 2 and G protein pathway suppressor 1 were significantly and positively associated with COPS6 expression level. These genes were predominantly involved in processes, such as ubiquitin-mediated proteolysis and human immunodeficiency virus 1 infection. CONCLUSION: In conclusion, this study systematically explored the significance of COPS6 across different tumor types, providing a solid foundation for considering COPS6 as a novel biomarker in cancer research. Baishideng Publishing Group Inc 2023-11-24 2023-11-24 /pmc/articles/PMC10696221/ http://dx.doi.org/10.5306/wjco.v14.i11.479 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Wang, Shi-Lin
Zhuo, Guang-Zheng
Wang, Li-Ping
Jiang, Xiang-Hu
Liu, Guo-Hong
Pan, Yun-Bao
Li, Yi-Rong
Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types
title Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types
title_full Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types
title_fullStr Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types
title_full_unstemmed Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types
title_short Computational exploration of the significance of COPS6 in cancer: Functional and clinical relevance across tumor types
title_sort computational exploration of the significance of cops6 in cancer: functional and clinical relevance across tumor types
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696221/
http://dx.doi.org/10.5306/wjco.v14.i11.479
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