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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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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. |
format | Online Article Text |
id | pubmed-4736761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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