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SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma
SOX2 copy number and mRNA expression were analysed to examine the clinical significance of SOX2 activation in HNSCC. Gene expression signatures reflecting SOX2 activation were identified in an HNSCC cohort. Patients with HNSCC were classified into two subgroups according to the gene expression signa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785960/ https://www.ncbi.nlm.nih.gov/pubmed/29374236 http://dx.doi.org/10.1038/s41598-018-20086-w |
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author | Chung, Ji Hyun Jung, Hae Rim Jung, Ah Ra Lee, Young Chan Kong, Moonkyoo Lee, Ju-Seog Eun, Young-Gyu |
author_facet | Chung, Ji Hyun Jung, Hae Rim Jung, Ah Ra Lee, Young Chan Kong, Moonkyoo Lee, Ju-Seog Eun, Young-Gyu |
author_sort | Chung, Ji Hyun |
collection | PubMed |
description | SOX2 copy number and mRNA expression were analysed to examine the clinical significance of SOX2 activation in HNSCC. Gene expression signatures reflecting SOX2 activation were identified in an HNSCC cohort. Patients with HNSCC were classified into two subgroups according to the gene expression signature: SOX2-high and SOX2-low. The clinical significance of SOX2 activation was further validated in two independent cohorts. Moreover, clinical significance of SOX2 activation in response to radiotherapy was assessed in patients with HNSCC. The relationship between SOX2 activation and radiotherapy was validated in an in vitro experiment. Patients in the SOX2-high subgroup had a better prognosis than patients in the SOX2-low subgroup in all three patient cohorts. Results of multivariate regression analysis showed that SOX2 signature was an independent predictor of the overall survival of patients with HNSCC (hazard ratio, 1.45; 95% confidence interval, 1.09–1.92; P = 0.01). Interestingly, SOX2 activation was a predictor of therapy outcomes in patients receiving radiotherapy. Moreover, SOX2 overexpression enhanced the effect of radiotherapy in HNSCC cell lines. SOX2 activation is associated with improved prognosis of patients with HNSCC and might be used to predict which patients might benefit from radiotherapy. |
format | Online Article Text |
id | pubmed-5785960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57859602018-02-07 SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma Chung, Ji Hyun Jung, Hae Rim Jung, Ah Ra Lee, Young Chan Kong, Moonkyoo Lee, Ju-Seog Eun, Young-Gyu Sci Rep Article SOX2 copy number and mRNA expression were analysed to examine the clinical significance of SOX2 activation in HNSCC. Gene expression signatures reflecting SOX2 activation were identified in an HNSCC cohort. Patients with HNSCC were classified into two subgroups according to the gene expression signature: SOX2-high and SOX2-low. The clinical significance of SOX2 activation was further validated in two independent cohorts. Moreover, clinical significance of SOX2 activation in response to radiotherapy was assessed in patients with HNSCC. The relationship between SOX2 activation and radiotherapy was validated in an in vitro experiment. Patients in the SOX2-high subgroup had a better prognosis than patients in the SOX2-low subgroup in all three patient cohorts. Results of multivariate regression analysis showed that SOX2 signature was an independent predictor of the overall survival of patients with HNSCC (hazard ratio, 1.45; 95% confidence interval, 1.09–1.92; P = 0.01). Interestingly, SOX2 activation was a predictor of therapy outcomes in patients receiving radiotherapy. Moreover, SOX2 overexpression enhanced the effect of radiotherapy in HNSCC cell lines. SOX2 activation is associated with improved prognosis of patients with HNSCC and might be used to predict which patients might benefit from radiotherapy. Nature Publishing Group UK 2018-01-26 /pmc/articles/PMC5785960/ /pubmed/29374236 http://dx.doi.org/10.1038/s41598-018-20086-w Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chung, Ji Hyun Jung, Hae Rim Jung, Ah Ra Lee, Young Chan Kong, Moonkyoo Lee, Ju-Seog Eun, Young-Gyu SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
title | SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
title_full | SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
title_fullStr | SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
title_full_unstemmed | SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
title_short | SOX2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
title_sort | sox2 activation predicts prognosis in patients with head and neck squamous cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785960/ https://www.ncbi.nlm.nih.gov/pubmed/29374236 http://dx.doi.org/10.1038/s41598-018-20086-w |
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