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The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database
N6-methyladenosine (m6A) modifications play an essential role in tumorigenesis. These modifications modulate RNAs, including mRNAs and lncRNAs. However, the prognostic role of m6A-related lncRNAs in head and neck squamous cell carcinoma (HNSCC) is poorly understood. Based on LASSO Cox regression, en...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755759/ https://www.ncbi.nlm.nih.gov/pubmed/35022464 http://dx.doi.org/10.1038/s41598-021-04591-z |
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author | Zhou, Liu-qing Shen, Jin-xiong Zhou, Jie-yu Hu, Yao Xiao, Hong-jun |
author_facet | Zhou, Liu-qing Shen, Jin-xiong Zhou, Jie-yu Hu, Yao Xiao, Hong-jun |
author_sort | Zhou, Liu-qing |
collection | PubMed |
description | N6-methyladenosine (m6A) modifications play an essential role in tumorigenesis. These modifications modulate RNAs, including mRNAs and lncRNAs. However, the prognostic role of m6A-related lncRNAs in head and neck squamous cell carcinoma (HNSCC) is poorly understood. Based on LASSO Cox regression, enrichment analysis, univariate and multivariate Cox regression analysis, a prognostic risk model, and consensus clustering analysis, we analyzed 12 m6A-related lncRNAs in HNSCC sample data from The Cancer Genome Atlas (TCGA) database. We found 12 m6A-related lncRNAs in the training cohort and validated them in all cohorts by Kaplan–Meier and Cox regression analyses, revealing their independent prognostic value in HNSCC. Moreover, ROC analysis was conducted, confirming the strong predictive ability of this signature for HNSCC survival. GSEA and detailed immune infiltration analyses revealed specific pathways associated with m6A-related lncRNAs. In this study, a novel risk model including twelve genes (SAP30L-AS1, AC022098.1, LINC01475, AC090587.2, AC008115.3, AC015911.3, AL122035.2, AC010226.1, AL513190.1, ZNF32-AS1, AL035587.1 and AL031716.1) was built. It could accurately predict HNSCC outcomes and could provide new therapeutic targets for HNSCC patients. |
format | Online Article Text |
id | pubmed-8755759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87557592022-01-14 The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database Zhou, Liu-qing Shen, Jin-xiong Zhou, Jie-yu Hu, Yao Xiao, Hong-jun Sci Rep Article N6-methyladenosine (m6A) modifications play an essential role in tumorigenesis. These modifications modulate RNAs, including mRNAs and lncRNAs. However, the prognostic role of m6A-related lncRNAs in head and neck squamous cell carcinoma (HNSCC) is poorly understood. Based on LASSO Cox regression, enrichment analysis, univariate and multivariate Cox regression analysis, a prognostic risk model, and consensus clustering analysis, we analyzed 12 m6A-related lncRNAs in HNSCC sample data from The Cancer Genome Atlas (TCGA) database. We found 12 m6A-related lncRNAs in the training cohort and validated them in all cohorts by Kaplan–Meier and Cox regression analyses, revealing their independent prognostic value in HNSCC. Moreover, ROC analysis was conducted, confirming the strong predictive ability of this signature for HNSCC survival. GSEA and detailed immune infiltration analyses revealed specific pathways associated with m6A-related lncRNAs. In this study, a novel risk model including twelve genes (SAP30L-AS1, AC022098.1, LINC01475, AC090587.2, AC008115.3, AC015911.3, AL122035.2, AC010226.1, AL513190.1, ZNF32-AS1, AL035587.1 and AL031716.1) was built. It could accurately predict HNSCC outcomes and could provide new therapeutic targets for HNSCC patients. Nature Publishing Group UK 2022-01-12 /pmc/articles/PMC8755759/ /pubmed/35022464 http://dx.doi.org/10.1038/s41598-021-04591-z Text en © The Author(s) 2022 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/) . |
spellingShingle | Article Zhou, Liu-qing Shen, Jin-xiong Zhou, Jie-yu Hu, Yao Xiao, Hong-jun The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database |
title | The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database |
title_full | The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database |
title_fullStr | The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database |
title_full_unstemmed | The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database |
title_short | The prognostic value of m6A-related LncRNAs in patients with HNSCC: bioinformatics analysis of TCGA database |
title_sort | prognostic value of m6a-related lncrnas in patients with hnscc: bioinformatics analysis of tcga database |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755759/ https://www.ncbi.nlm.nih.gov/pubmed/35022464 http://dx.doi.org/10.1038/s41598-021-04591-z |
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