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The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma
PURPOSE: Head and neck squamous cell carcinoma (HNSCC) is the sixth most prevalent cancer in the world, accounting for more than 90% of head and neck malignant tumors. However, its molecular mechanism is largely unknown. To help elucidate the potential mechanism of HNSCC tumorigenesis, we investigat...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689548/ https://www.ncbi.nlm.nih.gov/pubmed/31496804 http://dx.doi.org/10.2147/CMAR.S201177 |
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author | Song, Yidan Pan, Yihua Liu, Jun |
author_facet | Song, Yidan Pan, Yihua Liu, Jun |
author_sort | Song, Yidan |
collection | PubMed |
description | PURPOSE: Head and neck squamous cell carcinoma (HNSCC) is the sixth most prevalent cancer in the world, accounting for more than 90% of head and neck malignant tumors. However, its molecular mechanism is largely unknown. To help elucidate the potential mechanism of HNSCC tumorigenesis, we investigated the gene interaction patterns associated with tumorigenesis. METHODS: Weighted gene co-expression network analysis (WGCNA) can help us to predict the intrinsic relationship or correlation between gene expression. Additionally, we further explored the combination of clinical information and module construction. RESULTS: Sixteen modules were constructed, among which the key module most closely associated with clinical information was identified. By analyzing the genes in this module, we found that the latter may be related to the immune response, inflammatory response and formation of the tumor microenvironment. Sixteen hub genes were identified—ARHGAP9, SASH3, CORO1A, ITGAL, PPP1R16B, TBC1D10C, IL10RA, ITK, AKNA, PRKCB, TRAF3IP3, GIMAP4, CCR7, P2RY8, GIMAP7, and SP140. We further validated these genes at the transcriptional and translation levels. CONCLUSION: The innovative use of a weighted network to analyze HNSCC samples provides new insights into the molecular mechanism and prognosis of HNSCC. Additionally, the hub genes we identified can be used as biomarkers and therapeutic targets of HNSCC, laying the foundation for the accurate diagnosis and treatment of HNSCC in clinical and research in the future. |
format | Online Article Text |
id | pubmed-6689548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66895482019-09-06 The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma Song, Yidan Pan, Yihua Liu, Jun Cancer Manag Res Original Research PURPOSE: Head and neck squamous cell carcinoma (HNSCC) is the sixth most prevalent cancer in the world, accounting for more than 90% of head and neck malignant tumors. However, its molecular mechanism is largely unknown. To help elucidate the potential mechanism of HNSCC tumorigenesis, we investigated the gene interaction patterns associated with tumorigenesis. METHODS: Weighted gene co-expression network analysis (WGCNA) can help us to predict the intrinsic relationship or correlation between gene expression. Additionally, we further explored the combination of clinical information and module construction. RESULTS: Sixteen modules were constructed, among which the key module most closely associated with clinical information was identified. By analyzing the genes in this module, we found that the latter may be related to the immune response, inflammatory response and formation of the tumor microenvironment. Sixteen hub genes were identified—ARHGAP9, SASH3, CORO1A, ITGAL, PPP1R16B, TBC1D10C, IL10RA, ITK, AKNA, PRKCB, TRAF3IP3, GIMAP4, CCR7, P2RY8, GIMAP7, and SP140. We further validated these genes at the transcriptional and translation levels. CONCLUSION: The innovative use of a weighted network to analyze HNSCC samples provides new insights into the molecular mechanism and prognosis of HNSCC. Additionally, the hub genes we identified can be used as biomarkers and therapeutic targets of HNSCC, laying the foundation for the accurate diagnosis and treatment of HNSCC in clinical and research in the future. Dove 2019-08-06 /pmc/articles/PMC6689548/ /pubmed/31496804 http://dx.doi.org/10.2147/CMAR.S201177 Text en © 2019 Song et al. http://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/). 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 Song, Yidan Pan, Yihua Liu, Jun The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
title | The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
title_full | The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
title_fullStr | The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
title_full_unstemmed | The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
title_short | The relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
title_sort | relevance between the immune response-related gene module and clinical traits in head and neck squamous cell carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689548/ https://www.ncbi.nlm.nih.gov/pubmed/31496804 http://dx.doi.org/10.2147/CMAR.S201177 |
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