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A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients

Head and neck squamous cell carcinoma (HNSCC) is one of the most malignant cancers with poor prognosis worldwide. Emerging evidence indicates that competing endogenous RNAs (ceRNAs) are involved in various diseases, however, the regulatory mechanisms of ceRNAs underlying HNSCC remain unclear. In thi...

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Autores principales: Xu, Yuzi, Xu, Fengqin, Lv, Yiming, Wang, Siyuan, Li, Jia, Zhou, Chuan, Jiang, Jimin, Xie, Binbin, He, Fuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973582/
https://www.ncbi.nlm.nih.gov/pubmed/33737696
http://dx.doi.org/10.1038/s41598-021-86048-x
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author Xu, Yuzi
Xu, Fengqin
Lv, Yiming
Wang, Siyuan
Li, Jia
Zhou, Chuan
Jiang, Jimin
Xie, Binbin
He, Fuming
author_facet Xu, Yuzi
Xu, Fengqin
Lv, Yiming
Wang, Siyuan
Li, Jia
Zhou, Chuan
Jiang, Jimin
Xie, Binbin
He, Fuming
author_sort Xu, Yuzi
collection PubMed
description Head and neck squamous cell carcinoma (HNSCC) is one of the most malignant cancers with poor prognosis worldwide. Emerging evidence indicates that competing endogenous RNAs (ceRNAs) are involved in various diseases, however, the regulatory mechanisms of ceRNAs underlying HNSCC remain unclear. In this study, we retrieved differentially expressed long non-coding RNAs (DElncRNAs), messenger RNAs (DEmRNAs) and microRANs (DEmiRNAs) from The Cancer Genome Atlas database and constructed a ceRNA-based risk model in HNSCC by integrated bioinformatics approaches. Functional enrichment analyses showed that DEmRNAs might be involved in extracellular matrix related biological processes, and protein–protein interaction network further selected out prognostic genes, including MYL1 and ACTN2. Importantly, co-expressed RNAs identified by weighted co-expression gene network analysis constructed the ceRNA networks. Moreover, AC114730.3, AC136375.3, LAT and RYR3 were highly correlated to overall survival of HNSCC by Kaplan–Meier method and univariate Cox regression analysis, which were subsequently implemented multivariate Cox regression analysis to build the risk model. Our study provides a deeper understanding of ceRNAs on the regulatory mechanisms, which will facilitate the expansion of the roles on the ceRNAs in the tumorigenesis, development and treatment of HNSCC.
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spelling pubmed-79735822021-03-19 A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients Xu, Yuzi Xu, Fengqin Lv, Yiming Wang, Siyuan Li, Jia Zhou, Chuan Jiang, Jimin Xie, Binbin He, Fuming Sci Rep Article Head and neck squamous cell carcinoma (HNSCC) is one of the most malignant cancers with poor prognosis worldwide. Emerging evidence indicates that competing endogenous RNAs (ceRNAs) are involved in various diseases, however, the regulatory mechanisms of ceRNAs underlying HNSCC remain unclear. In this study, we retrieved differentially expressed long non-coding RNAs (DElncRNAs), messenger RNAs (DEmRNAs) and microRANs (DEmiRNAs) from The Cancer Genome Atlas database and constructed a ceRNA-based risk model in HNSCC by integrated bioinformatics approaches. Functional enrichment analyses showed that DEmRNAs might be involved in extracellular matrix related biological processes, and protein–protein interaction network further selected out prognostic genes, including MYL1 and ACTN2. Importantly, co-expressed RNAs identified by weighted co-expression gene network analysis constructed the ceRNA networks. Moreover, AC114730.3, AC136375.3, LAT and RYR3 were highly correlated to overall survival of HNSCC by Kaplan–Meier method and univariate Cox regression analysis, which were subsequently implemented multivariate Cox regression analysis to build the risk model. Our study provides a deeper understanding of ceRNAs on the regulatory mechanisms, which will facilitate the expansion of the roles on the ceRNAs in the tumorigenesis, development and treatment of HNSCC. Nature Publishing Group UK 2021-03-18 /pmc/articles/PMC7973582/ /pubmed/33737696 http://dx.doi.org/10.1038/s41598-021-86048-x Text en © The Author(s) 2021 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/.
spellingShingle Article
Xu, Yuzi
Xu, Fengqin
Lv, Yiming
Wang, Siyuan
Li, Jia
Zhou, Chuan
Jiang, Jimin
Xie, Binbin
He, Fuming
A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
title A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
title_full A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
title_fullStr A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
title_full_unstemmed A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
title_short A ceRNA-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
title_sort cerna-associated risk model predicts the poor prognosis for head and neck squamous cell carcinoma patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973582/
https://www.ncbi.nlm.nih.gov/pubmed/33737696
http://dx.doi.org/10.1038/s41598-021-86048-x
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