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A HPV16-related prognostic indicator for head and neck squamous cell carcinoma
BACKGROUND: The human papillomavirus (HPV) is emerging as an important risk factor in head and neck squamous cell carcinoma (HNSCC) patients. This has been observed particularly in the case of HPV16. The HPV16+ HNSCC subtype has distinct pathological, clinical, molecular, and prognostic characterist...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729314/ https://www.ncbi.nlm.nih.gov/pubmed/33313237 http://dx.doi.org/10.21037/atm-20-6338 |
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author | Zhang, Qian Chen, Yongfeng Hu, Shi-Qi Pu, Yu-Mei Zhang, Kai Wang, Yu-Xin |
author_facet | Zhang, Qian Chen, Yongfeng Hu, Shi-Qi Pu, Yu-Mei Zhang, Kai Wang, Yu-Xin |
author_sort | Zhang, Qian |
collection | PubMed |
description | BACKGROUND: The human papillomavirus (HPV) is emerging as an important risk factor in head and neck squamous cell carcinoma (HNSCC) patients. This has been observed particularly in the case of HPV16. The HPV16+ HNSCC subtype has distinct pathological, clinical, molecular, and prognostic characteristics. This study aimed to identify potential microRNAs (miRNAs) and their roles in HPV16+ HNSCC progression. METHOD: miRNA, mRNA and the clinical data of 519 HNSCC and 44 HNSCC-negative samples were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed miRNAs (DEMs) in HPV16-related HNSCC tissues with prognostic value were selected. DEM levels were assessed based on clinicopathological parameters and overall survival (OS). Target genes were also predicted and functional analysis based on Gene Set Enrichment Analysis (GSEA) were then performed. RESULTS: In HPV16+ HNSCC tissues, miR-99a-3p and miR-4746-5p were significantly upregulated. In contrast, miR-411-5p was shown to be downregulated. miR-99a-3p(high)miR-411-5p(low)miR-4746-5p(high) expression could estimate improved OS and low frequent perineural invasion (PNI). Predicted target genes were enriched in cell growth, neuroepithelial cell differentiation, MAPK and FoxO signaling pathways. Epithelial mesenchymal transition (EMT) gene set and invasion related genes were downregulated in miR-99a-3p(high)miR-411-5p(low)miR-4746-5p(high) HNSCC patients. CONCLUSION: miR-99a-3p, miR-411-5p and miR-4746-5p might participate in HPV16+ HNSCC progression through EMT related pathways and affect prognosis. |
format | Online Article Text |
id | pubmed-7729314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-77293142020-12-11 A HPV16-related prognostic indicator for head and neck squamous cell carcinoma Zhang, Qian Chen, Yongfeng Hu, Shi-Qi Pu, Yu-Mei Zhang, Kai Wang, Yu-Xin Ann Transl Med Original Article BACKGROUND: The human papillomavirus (HPV) is emerging as an important risk factor in head and neck squamous cell carcinoma (HNSCC) patients. This has been observed particularly in the case of HPV16. The HPV16+ HNSCC subtype has distinct pathological, clinical, molecular, and prognostic characteristics. This study aimed to identify potential microRNAs (miRNAs) and their roles in HPV16+ HNSCC progression. METHOD: miRNA, mRNA and the clinical data of 519 HNSCC and 44 HNSCC-negative samples were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed miRNAs (DEMs) in HPV16-related HNSCC tissues with prognostic value were selected. DEM levels were assessed based on clinicopathological parameters and overall survival (OS). Target genes were also predicted and functional analysis based on Gene Set Enrichment Analysis (GSEA) were then performed. RESULTS: In HPV16+ HNSCC tissues, miR-99a-3p and miR-4746-5p were significantly upregulated. In contrast, miR-411-5p was shown to be downregulated. miR-99a-3p(high)miR-411-5p(low)miR-4746-5p(high) expression could estimate improved OS and low frequent perineural invasion (PNI). Predicted target genes were enriched in cell growth, neuroepithelial cell differentiation, MAPK and FoxO signaling pathways. Epithelial mesenchymal transition (EMT) gene set and invasion related genes were downregulated in miR-99a-3p(high)miR-411-5p(low)miR-4746-5p(high) HNSCC patients. CONCLUSION: miR-99a-3p, miR-411-5p and miR-4746-5p might participate in HPV16+ HNSCC progression through EMT related pathways and affect prognosis. AME Publishing Company 2020-11 /pmc/articles/PMC7729314/ /pubmed/33313237 http://dx.doi.org/10.21037/atm-20-6338 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Zhang, Qian Chen, Yongfeng Hu, Shi-Qi Pu, Yu-Mei Zhang, Kai Wang, Yu-Xin A HPV16-related prognostic indicator for head and neck squamous cell carcinoma |
title | A HPV16-related prognostic indicator for head and neck squamous cell carcinoma |
title_full | A HPV16-related prognostic indicator for head and neck squamous cell carcinoma |
title_fullStr | A HPV16-related prognostic indicator for head and neck squamous cell carcinoma |
title_full_unstemmed | A HPV16-related prognostic indicator for head and neck squamous cell carcinoma |
title_short | A HPV16-related prognostic indicator for head and neck squamous cell carcinoma |
title_sort | hpv16-related prognostic indicator for head and neck squamous cell carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729314/ https://www.ncbi.nlm.nih.gov/pubmed/33313237 http://dx.doi.org/10.21037/atm-20-6338 |
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