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Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers

A growing proportion of head and neck cancers (HNC) result from HPV infection. Between HNC aetiological groups (HPV positive and HPV negative) clinical evidence demonstrates significantly better treatment response among HPV positive cancers. Cancer stem cells (CSCs) are identified in HNC tumour popu...

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Autores principales: Reid, Paul, Staudacher, Alexander H., Marcu, Loredana G., Olver, Ian, Moghaddasi, Leyla, Brown, Michael P., Bezak, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026429/
https://www.ncbi.nlm.nih.gov/pubmed/32066820
http://dx.doi.org/10.1038/s41598-020-59654-4
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author Reid, Paul
Staudacher, Alexander H.
Marcu, Loredana G.
Olver, Ian
Moghaddasi, Leyla
Brown, Michael P.
Bezak, Eva
author_facet Reid, Paul
Staudacher, Alexander H.
Marcu, Loredana G.
Olver, Ian
Moghaddasi, Leyla
Brown, Michael P.
Bezak, Eva
author_sort Reid, Paul
collection PubMed
description A growing proportion of head and neck cancers (HNC) result from HPV infection. Between HNC aetiological groups (HPV positive and HPV negative) clinical evidence demonstrates significantly better treatment response among HPV positive cancers. Cancer stem cells (CSCs) are identified in HNC tumour populations as agents of treatment resistance and a target for tumour control. This study examines dynamic responses in populations of a CSC phenotype in HNC cell lines following X-irradiation at therapeutic levels, and comparing between HPV statuses. Variations in CSC density between HPV groups showed no correlation with better clinical outcomes seen in the HPV positive status. CSC populations in HPV positive cell lines ranged from 1.9 to 4.8%, and 2.6 to 9.9% for HPV negative. Following 4 Gy X- irradiation however, HPV negative cell lines demonstrated more frequent and significantly greater escalation in CSC proportions, being 3-fold that of the HPV positive group at 72 hours post irradiation. CSC proportions of tumour populations are not fixed but subject to change in response to radiation at therapeutic dose levels. These findings imply a potential effect of aetiology on radio-responsiveness in CSCs, illustrating that clonogen treatment response may be more informative of therapy outcomes than inherent population density alone.
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spelling pubmed-70264292020-02-26 Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers Reid, Paul Staudacher, Alexander H. Marcu, Loredana G. Olver, Ian Moghaddasi, Leyla Brown, Michael P. Bezak, Eva Sci Rep Article A growing proportion of head and neck cancers (HNC) result from HPV infection. Between HNC aetiological groups (HPV positive and HPV negative) clinical evidence demonstrates significantly better treatment response among HPV positive cancers. Cancer stem cells (CSCs) are identified in HNC tumour populations as agents of treatment resistance and a target for tumour control. This study examines dynamic responses in populations of a CSC phenotype in HNC cell lines following X-irradiation at therapeutic levels, and comparing between HPV statuses. Variations in CSC density between HPV groups showed no correlation with better clinical outcomes seen in the HPV positive status. CSC populations in HPV positive cell lines ranged from 1.9 to 4.8%, and 2.6 to 9.9% for HPV negative. Following 4 Gy X- irradiation however, HPV negative cell lines demonstrated more frequent and significantly greater escalation in CSC proportions, being 3-fold that of the HPV positive group at 72 hours post irradiation. CSC proportions of tumour populations are not fixed but subject to change in response to radiation at therapeutic dose levels. These findings imply a potential effect of aetiology on radio-responsiveness in CSCs, illustrating that clonogen treatment response may be more informative of therapy outcomes than inherent population density alone. Nature Publishing Group UK 2020-02-17 /pmc/articles/PMC7026429/ /pubmed/32066820 http://dx.doi.org/10.1038/s41598-020-59654-4 Text en © The Author(s) 2020 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
Reid, Paul
Staudacher, Alexander H.
Marcu, Loredana G.
Olver, Ian
Moghaddasi, Leyla
Brown, Michael P.
Bezak, Eva
Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
title Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
title_full Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
title_fullStr Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
title_full_unstemmed Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
title_short Influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
title_sort influence of the human papillomavirus on the radio-responsiveness of cancer stem cells in head and neck cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026429/
https://www.ncbi.nlm.nih.gov/pubmed/32066820
http://dx.doi.org/10.1038/s41598-020-59654-4
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