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HOPX functions as a tumour suppressor in head and neck cancer
Head and neck squamous cell carcinoma (HNSCC) is generalized term that encompasses a diverse group of cancers that includes tumours of the oral cavity (OSCC), oropharynx (OPSCC) and nasopharynx (NPC). Genetic alterations that are common to all HNSCC types are likely to be important for squamous carc...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146930/ https://www.ncbi.nlm.nih.gov/pubmed/27934959 http://dx.doi.org/10.1038/srep38758 |
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author | Yap, Lee Fah Lai, Sook Ling Patmanathan, Sathya Narayanan Gokulan, Ravindran Robinson, C. Max White, Joe B. Chai, San Jiun Rajadurai, Pathmanathan Prepageran, Narayanan Liew, Yew Toong Lopes, Victor Wei, Wenbin Hollows, Robert J. Murray, Paul G. Lambert, Daniel W. Hunter, Keith D. Paterson, Ian C. |
author_facet | Yap, Lee Fah Lai, Sook Ling Patmanathan, Sathya Narayanan Gokulan, Ravindran Robinson, C. Max White, Joe B. Chai, San Jiun Rajadurai, Pathmanathan Prepageran, Narayanan Liew, Yew Toong Lopes, Victor Wei, Wenbin Hollows, Robert J. Murray, Paul G. Lambert, Daniel W. Hunter, Keith D. Paterson, Ian C. |
author_sort | Yap, Lee Fah |
collection | PubMed |
description | Head and neck squamous cell carcinoma (HNSCC) is generalized term that encompasses a diverse group of cancers that includes tumours of the oral cavity (OSCC), oropharynx (OPSCC) and nasopharynx (NPC). Genetic alterations that are common to all HNSCC types are likely to be important for squamous carcinogenesis. In this study, we have investigated the role of the homeodomain-only homeobox gene, HOPX, in the pathogenesis of HNSCC. We show that HOPX mRNA levels are reduced in OSCC and NPC cell lines and tissues and there is a general reduction of HOPX protein expression in these tumours and OPSCCs. HOPX promoter methylation was observed in a subset of HNSCCs and was associated with a worse overall survival in HPV negative tumours. RNAseq analysis of OSCC cells transfected with HOPX revealed a widespread deregulation of the transcription of genes related to epithelial homeostasis and ectopic over-expression of HOPX in OSCC and NPC cells inhibited cell proliferation, plating efficiency and migration, and enhanced sensitivity to UVA-induced apoptosis. Our results demonstrate that HOPX functions as a tumour suppressor in HNSCC and suggest a central role for HOPX in suppressing epithelial carcinogenesis. |
format | Online Article Text |
id | pubmed-5146930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51469302016-12-16 HOPX functions as a tumour suppressor in head and neck cancer Yap, Lee Fah Lai, Sook Ling Patmanathan, Sathya Narayanan Gokulan, Ravindran Robinson, C. Max White, Joe B. Chai, San Jiun Rajadurai, Pathmanathan Prepageran, Narayanan Liew, Yew Toong Lopes, Victor Wei, Wenbin Hollows, Robert J. Murray, Paul G. Lambert, Daniel W. Hunter, Keith D. Paterson, Ian C. Sci Rep Article Head and neck squamous cell carcinoma (HNSCC) is generalized term that encompasses a diverse group of cancers that includes tumours of the oral cavity (OSCC), oropharynx (OPSCC) and nasopharynx (NPC). Genetic alterations that are common to all HNSCC types are likely to be important for squamous carcinogenesis. In this study, we have investigated the role of the homeodomain-only homeobox gene, HOPX, in the pathogenesis of HNSCC. We show that HOPX mRNA levels are reduced in OSCC and NPC cell lines and tissues and there is a general reduction of HOPX protein expression in these tumours and OPSCCs. HOPX promoter methylation was observed in a subset of HNSCCs and was associated with a worse overall survival in HPV negative tumours. RNAseq analysis of OSCC cells transfected with HOPX revealed a widespread deregulation of the transcription of genes related to epithelial homeostasis and ectopic over-expression of HOPX in OSCC and NPC cells inhibited cell proliferation, plating efficiency and migration, and enhanced sensitivity to UVA-induced apoptosis. Our results demonstrate that HOPX functions as a tumour suppressor in HNSCC and suggest a central role for HOPX in suppressing epithelial carcinogenesis. Nature Publishing Group 2016-12-09 /pmc/articles/PMC5146930/ /pubmed/27934959 http://dx.doi.org/10.1038/srep38758 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yap, Lee Fah Lai, Sook Ling Patmanathan, Sathya Narayanan Gokulan, Ravindran Robinson, C. Max White, Joe B. Chai, San Jiun Rajadurai, Pathmanathan Prepageran, Narayanan Liew, Yew Toong Lopes, Victor Wei, Wenbin Hollows, Robert J. Murray, Paul G. Lambert, Daniel W. Hunter, Keith D. Paterson, Ian C. HOPX functions as a tumour suppressor in head and neck cancer |
title | HOPX functions as a tumour suppressor in head and neck cancer |
title_full | HOPX functions as a tumour suppressor in head and neck cancer |
title_fullStr | HOPX functions as a tumour suppressor in head and neck cancer |
title_full_unstemmed | HOPX functions as a tumour suppressor in head and neck cancer |
title_short | HOPX functions as a tumour suppressor in head and neck cancer |
title_sort | hopx functions as a tumour suppressor in head and neck cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146930/ https://www.ncbi.nlm.nih.gov/pubmed/27934959 http://dx.doi.org/10.1038/srep38758 |
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