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Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer

The aim of the study was to investigate cancer stem signaling during the repopulation response of a head and neck squamous cell cancer (HNSCC) xenograft after radiation treatment. Xenografts were generated from low passage HNSCC cells and were treated with either sham radiation or 15 Gy in one fract...

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Autores principales: Wilson, George D., Thibodeau, Bryan J., Fortier, Laura E., Pruetz, Barbara L., Galoforo, Sandra, Marples, Brian, Baschnagel, Andrew M., Akervall, Jan, Huang, Jiayi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736761/
https://www.ncbi.nlm.nih.gov/pubmed/26880935
http://dx.doi.org/10.1155/2016/1894782
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author Wilson, George D.
Thibodeau, Bryan J.
Fortier, Laura E.
Pruetz, Barbara L.
Galoforo, Sandra
Marples, Brian
Baschnagel, Andrew M.
Akervall, Jan
Huang, Jiayi
author_facet Wilson, George D.
Thibodeau, Bryan J.
Fortier, Laura E.
Pruetz, Barbara L.
Galoforo, Sandra
Marples, Brian
Baschnagel, Andrew M.
Akervall, Jan
Huang, Jiayi
author_sort Wilson, George D.
collection PubMed
description The aim of the study was to investigate cancer stem signaling during the repopulation response of a head and neck squamous cell cancer (HNSCC) xenograft after radiation treatment. Xenografts were generated from low passage HNSCC cells and were treated with either sham radiation or 15 Gy in one fraction. At different time points, days 0, 3, and 10 for controls and days 4, 7, 12, and 21, after irradiation, 3 tumors per group were harvested for global gene expression, pathway analysis, and immunohistochemical evaluation. 316 genes were identified that were associated with a series of stem cell-related genes and were differentially expressed (p ≤ 0.01 and 1.5-fold) at a minimum of one time point in UT-SCC-14 xenografts after radiation. The largest network of genes that showed significant changes after irradiation was associated with CD44, NOTCH1, and MET. c-MET and ALDH1A3 staining correlated with the changes in gene expression. A clear pattern emerged that was consistent with the growth inhibition data in that genes associated with stem cell pathways were most active at day 7 and day 12 after irradiation. The MET/CD44 axis seemed to be an important component of the repopulation response.
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spelling pubmed-47367612016-02-15 Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer Wilson, George D. Thibodeau, Bryan J. Fortier, Laura E. Pruetz, Barbara L. Galoforo, Sandra Marples, Brian Baschnagel, Andrew M. Akervall, Jan Huang, Jiayi Stem Cells Int Research Article The aim of the study was to investigate cancer stem signaling during the repopulation response of a head and neck squamous cell cancer (HNSCC) xenograft after radiation treatment. Xenografts were generated from low passage HNSCC cells and were treated with either sham radiation or 15 Gy in one fraction. At different time points, days 0, 3, and 10 for controls and days 4, 7, 12, and 21, after irradiation, 3 tumors per group were harvested for global gene expression, pathway analysis, and immunohistochemical evaluation. 316 genes were identified that were associated with a series of stem cell-related genes and were differentially expressed (p ≤ 0.01 and 1.5-fold) at a minimum of one time point in UT-SCC-14 xenografts after radiation. The largest network of genes that showed significant changes after irradiation was associated with CD44, NOTCH1, and MET. c-MET and ALDH1A3 staining correlated with the changes in gene expression. A clear pattern emerged that was consistent with the growth inhibition data in that genes associated with stem cell pathways were most active at day 7 and day 12 after irradiation. The MET/CD44 axis seemed to be an important component of the repopulation response. Hindawi Publishing Corporation 2016 2016-01-06 /pmc/articles/PMC4736761/ /pubmed/26880935 http://dx.doi.org/10.1155/2016/1894782 Text en Copyright © 2016 George D. Wilson et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wilson, George D.
Thibodeau, Bryan J.
Fortier, Laura E.
Pruetz, Barbara L.
Galoforo, Sandra
Marples, Brian
Baschnagel, Andrew M.
Akervall, Jan
Huang, Jiayi
Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer
title Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer
title_full Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer
title_fullStr Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer
title_full_unstemmed Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer
title_short Cancer Stem Cell Signaling during Repopulation in Head and Neck Cancer
title_sort cancer stem cell signaling during repopulation in head and neck cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736761/
https://www.ncbi.nlm.nih.gov/pubmed/26880935
http://dx.doi.org/10.1155/2016/1894782
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