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Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)

Cancer Stem Cells (CSCs) in Head and Neck Squamous Cell Carcinoma (HNSCC) have extremely aggressive profile (high migratory and invasive potential). These characteristics can explain their resistance to conventional treatment. Efficacy of photon and carbon ion irradiation with addition of cetuximab...

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Autores principales: Moncharmont, Coralie, Guy, Jean-Baptiste, Wozny, Anne-Sophie, Gilormini, Marion, Battiston-Montagne, Priscilla, Ardail, Dominique, Beuve, Michael, Alphonse, Gersende, Simoëns, Xavier, Rancoule, Chloé, Rodriguez-Lafrasse, Claire, Magné, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216975/
https://www.ncbi.nlm.nih.gov/pubmed/27374096
http://dx.doi.org/10.18632/oncotarget.10281
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author Moncharmont, Coralie
Guy, Jean-Baptiste
Wozny, Anne-Sophie
Gilormini, Marion
Battiston-Montagne, Priscilla
Ardail, Dominique
Beuve, Michael
Alphonse, Gersende
Simoëns, Xavier
Rancoule, Chloé
Rodriguez-Lafrasse, Claire
Magné, Nicolas
author_facet Moncharmont, Coralie
Guy, Jean-Baptiste
Wozny, Anne-Sophie
Gilormini, Marion
Battiston-Montagne, Priscilla
Ardail, Dominique
Beuve, Michael
Alphonse, Gersende
Simoëns, Xavier
Rancoule, Chloé
Rodriguez-Lafrasse, Claire
Magné, Nicolas
author_sort Moncharmont, Coralie
collection PubMed
description Cancer Stem Cells (CSCs) in Head and Neck Squamous Cell Carcinoma (HNSCC) have extremely aggressive profile (high migratory and invasive potential). These characteristics can explain their resistance to conventional treatment. Efficacy of photon and carbon ion irradiation with addition of cetuximab (5 nM) is studied on clonogenic death, migration and invasion of two HNSCC populations: SQ20B and SQ20B/CSCs. SQ20B express E-cadherin and overexpress EGFR while SQ20B/CSCs express N-cadherin and low EGFR. Cetuximab strongly inhibits SQ20B proliferation but has no effect on SQ20B/CSCs. 2 Gy photon irradiation enhances migration and invasiveness in both populations (p < 0.05), while cetuximab only stops SQ20B migration (p < 0.005). Carbon irradiation significantly inhibits invasion in both populations (p < 0.05), and the association with cetuximab significantly inhibits invasion in both populations (p < 0.005). These results highlight CSCs characteristics: EGFR(Low), cetuximab-resistant, and highly migratory. Carbon ion irradiation appears to be a very promising therapeutic modality counteracting migration/invasion process in both parental cells and CSCs in contrast to photon irradiation.
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spelling pubmed-52169752017-01-17 Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC) Moncharmont, Coralie Guy, Jean-Baptiste Wozny, Anne-Sophie Gilormini, Marion Battiston-Montagne, Priscilla Ardail, Dominique Beuve, Michael Alphonse, Gersende Simoëns, Xavier Rancoule, Chloé Rodriguez-Lafrasse, Claire Magné, Nicolas Oncotarget Research Paper Cancer Stem Cells (CSCs) in Head and Neck Squamous Cell Carcinoma (HNSCC) have extremely aggressive profile (high migratory and invasive potential). These characteristics can explain their resistance to conventional treatment. Efficacy of photon and carbon ion irradiation with addition of cetuximab (5 nM) is studied on clonogenic death, migration and invasion of two HNSCC populations: SQ20B and SQ20B/CSCs. SQ20B express E-cadherin and overexpress EGFR while SQ20B/CSCs express N-cadherin and low EGFR. Cetuximab strongly inhibits SQ20B proliferation but has no effect on SQ20B/CSCs. 2 Gy photon irradiation enhances migration and invasiveness in both populations (p < 0.05), while cetuximab only stops SQ20B migration (p < 0.005). Carbon irradiation significantly inhibits invasion in both populations (p < 0.05), and the association with cetuximab significantly inhibits invasion in both populations (p < 0.005). These results highlight CSCs characteristics: EGFR(Low), cetuximab-resistant, and highly migratory. Carbon ion irradiation appears to be a very promising therapeutic modality counteracting migration/invasion process in both parental cells and CSCs in contrast to photon irradiation. Impact Journals LLC 2016-06-24 /pmc/articles/PMC5216975/ /pubmed/27374096 http://dx.doi.org/10.18632/oncotarget.10281 Text en Copyright: © 2016 Moncharmont et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Moncharmont, Coralie
Guy, Jean-Baptiste
Wozny, Anne-Sophie
Gilormini, Marion
Battiston-Montagne, Priscilla
Ardail, Dominique
Beuve, Michael
Alphonse, Gersende
Simoëns, Xavier
Rancoule, Chloé
Rodriguez-Lafrasse, Claire
Magné, Nicolas
Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)
title Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)
title_full Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)
title_fullStr Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)
title_full_unstemmed Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)
title_short Carbon ion irradiation withstands cancer stem cells' migration/invasion process in Head and Neck Squamous Cell Carcinoma (HNSCC)
title_sort carbon ion irradiation withstands cancer stem cells' migration/invasion process in head and neck squamous cell carcinoma (hnscc)
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216975/
https://www.ncbi.nlm.nih.gov/pubmed/27374096
http://dx.doi.org/10.18632/oncotarget.10281
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