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Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma
Long non-coding RNAs (lncRNAs) are promising cancer prognostic markers. However, the clinical significance of lncRNA signatures in evaluating overall survival (OS) outcomes of head and neck squamous cell carcinoma (HNSCC) has not been explored. This study aimed to assess the significance of lncRNA i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809959/ https://www.ncbi.nlm.nih.gov/pubmed/34872450 http://dx.doi.org/10.1080/21655979.2021.1995577 |
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author | Wang, Jian Bian, Qinjiang Liu, Jialin Moming, Adili |
author_facet | Wang, Jian Bian, Qinjiang Liu, Jialin Moming, Adili |
author_sort | Wang, Jian |
collection | PubMed |
description | Long non-coding RNAs (lncRNAs) are promising cancer prognostic markers. However, the clinical significance of lncRNA signatures in evaluating overall survival (OS) outcomes of head and neck squamous cell carcinoma (HNSCC) has not been explored. This study aimed to assess the significance of lncRNA in HNSCC and to develop a lncRNA signature related to OS in HNSCC. LncRNA expression matrices were retrieved from the Cancer Genome Atlas (TCGA) data. Least Absolute Shrinkage and Selection of the Operator (LASSO), univariate and multivariate Cox regression were used for establishing a prognostic model. In vitro experiments were carried out to demonstrate the biological role of lncRNA. A prognosis model based on 7 DElncRNAs was finally established.The patients were then divided into high-risk and low-risk groups. Relative to the low-risk group, overall survival times for patients in the high-risk group were significantly low (P=2.466e−07). Risk score remained an independent prognostic factor in univariate (HR=1.329, 95%CI=1.239−1.425, p < 0.001) and multivariate (HR=1.279, 95%CI=1.184−1.382, p < 0.001) Cox regression analyses. The area under the curve (AUC) of the signature was as high as 0.78. Expressions of FOXD2-AS1 in tumor tissues were elevated, and significantly correlated with OS (P=0.008). FOXD2-AS1 silencing then significantly reduced HNSCC cell proliferation, invasion, and migration. In conclusion, a lncRNA signature was established for HNSCC prognostic prediction and FOXD2-AS1 was identified as an HNSCC oncogene. |
format | Online Article Text |
id | pubmed-8809959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-88099592022-02-03 Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma Wang, Jian Bian, Qinjiang Liu, Jialin Moming, Adili Bioengineered Research Paper Long non-coding RNAs (lncRNAs) are promising cancer prognostic markers. However, the clinical significance of lncRNA signatures in evaluating overall survival (OS) outcomes of head and neck squamous cell carcinoma (HNSCC) has not been explored. This study aimed to assess the significance of lncRNA in HNSCC and to develop a lncRNA signature related to OS in HNSCC. LncRNA expression matrices were retrieved from the Cancer Genome Atlas (TCGA) data. Least Absolute Shrinkage and Selection of the Operator (LASSO), univariate and multivariate Cox regression were used for establishing a prognostic model. In vitro experiments were carried out to demonstrate the biological role of lncRNA. A prognosis model based on 7 DElncRNAs was finally established.The patients were then divided into high-risk and low-risk groups. Relative to the low-risk group, overall survival times for patients in the high-risk group were significantly low (P=2.466e−07). Risk score remained an independent prognostic factor in univariate (HR=1.329, 95%CI=1.239−1.425, p < 0.001) and multivariate (HR=1.279, 95%CI=1.184−1.382, p < 0.001) Cox regression analyses. The area under the curve (AUC) of the signature was as high as 0.78. Expressions of FOXD2-AS1 in tumor tissues were elevated, and significantly correlated with OS (P=0.008). FOXD2-AS1 silencing then significantly reduced HNSCC cell proliferation, invasion, and migration. In conclusion, a lncRNA signature was established for HNSCC prognostic prediction and FOXD2-AS1 was identified as an HNSCC oncogene. Taylor & Francis 2021-12-07 /pmc/articles/PMC8809959/ /pubmed/34872450 http://dx.doi.org/10.1080/21655979.2021.1995577 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Wang, Jian Bian, Qinjiang Liu, Jialin Moming, Adili Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma |
title | Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma |
title_full | Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma |
title_fullStr | Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma |
title_full_unstemmed | Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma |
title_short | Identification and in vitro validation of prognostic lncRNA signature in head and neck squamous cell carcinoma |
title_sort | identification and in vitro validation of prognostic lncrna signature in head and neck squamous cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809959/ https://www.ncbi.nlm.nih.gov/pubmed/34872450 http://dx.doi.org/10.1080/21655979.2021.1995577 |
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