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Radiation-induced motility alterations in medulloblastoma cells
Photon irradiation has been repeatedly suspected of increasing tumor cell motility and promoting locoregional recurrence of disease. This study was set up to analyse possible mechanisms underlying the potentially radiation-altered motility in medulloblastoma cells. Medulloblastoma cell lines D425 an...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426914/ https://www.ncbi.nlm.nih.gov/pubmed/25736470 http://dx.doi.org/10.1093/jrr/rru120 |
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author | Rieken, Stefan Rieber, Juliane Brons, Stephan Habermehl, Daniel Rief, Harald Orschiedt, Lena Lindel, Katja Weber, Klaus J. Debus, Jürgen Combs, Stephanie E. |
author_facet | Rieken, Stefan Rieber, Juliane Brons, Stephan Habermehl, Daniel Rief, Harald Orschiedt, Lena Lindel, Katja Weber, Klaus J. Debus, Jürgen Combs, Stephanie E. |
author_sort | Rieken, Stefan |
collection | PubMed |
description | Photon irradiation has been repeatedly suspected of increasing tumor cell motility and promoting locoregional recurrence of disease. This study was set up to analyse possible mechanisms underlying the potentially radiation-altered motility in medulloblastoma cells. Medulloblastoma cell lines D425 and Med8A were analyzed in migration and adhesion experiments with and without photon and carbon ion irradiation. Expression of integrins was determined by quantitative FACS analysis. Matrix metalloproteinase concentrations within cell culture supernatants were investigated by enzyme-linked immunosorbent assay (ELISA). Statistical analysis was performed using Student's t-test. Both photon and carbon ion irradiation significantly reduced chemotactic medulloblastoma cell transmigration through 8-μm pore size membranes, while simultaneously increasing adherence to fibronectin- and collagen I- and IV–coated surfaces. Correspondingly, both photon and carbon ion irradiation downregulate soluble MMP9 concentrations, while upregulating cell surface expression of proadhesive extracellular matrix protein-binding integrin α(5). The observed phenotype of radiation-altered motility is more pronounced following carbon ion than photon irradiation. Both photon and (even more so) carbon ion irradiation are effective in inhibiting medulloblastoma cell migration through downregulation of matrix metalloproteinase 9 and upregulation of proadhesive cell surface integrin α5, which lead to increased cell adherence to extracellular matrix proteins. |
format | Online Article Text |
id | pubmed-4426914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44269142015-05-15 Radiation-induced motility alterations in medulloblastoma cells Rieken, Stefan Rieber, Juliane Brons, Stephan Habermehl, Daniel Rief, Harald Orschiedt, Lena Lindel, Katja Weber, Klaus J. Debus, Jürgen Combs, Stephanie E. J Radiat Res Biology Photon irradiation has been repeatedly suspected of increasing tumor cell motility and promoting locoregional recurrence of disease. This study was set up to analyse possible mechanisms underlying the potentially radiation-altered motility in medulloblastoma cells. Medulloblastoma cell lines D425 and Med8A were analyzed in migration and adhesion experiments with and without photon and carbon ion irradiation. Expression of integrins was determined by quantitative FACS analysis. Matrix metalloproteinase concentrations within cell culture supernatants were investigated by enzyme-linked immunosorbent assay (ELISA). Statistical analysis was performed using Student's t-test. Both photon and carbon ion irradiation significantly reduced chemotactic medulloblastoma cell transmigration through 8-μm pore size membranes, while simultaneously increasing adherence to fibronectin- and collagen I- and IV–coated surfaces. Correspondingly, both photon and carbon ion irradiation downregulate soluble MMP9 concentrations, while upregulating cell surface expression of proadhesive extracellular matrix protein-binding integrin α(5). The observed phenotype of radiation-altered motility is more pronounced following carbon ion than photon irradiation. Both photon and (even more so) carbon ion irradiation are effective in inhibiting medulloblastoma cell migration through downregulation of matrix metalloproteinase 9 and upregulation of proadhesive cell surface integrin α5, which lead to increased cell adherence to extracellular matrix proteins. Oxford University Press 2015-05 2015-03-02 /pmc/articles/PMC4426914/ /pubmed/25736470 http://dx.doi.org/10.1093/jrr/rru120 Text en © The Author 2015. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Biology Rieken, Stefan Rieber, Juliane Brons, Stephan Habermehl, Daniel Rief, Harald Orschiedt, Lena Lindel, Katja Weber, Klaus J. Debus, Jürgen Combs, Stephanie E. Radiation-induced motility alterations in medulloblastoma cells |
title | Radiation-induced motility alterations in medulloblastoma cells |
title_full | Radiation-induced motility alterations in medulloblastoma cells |
title_fullStr | Radiation-induced motility alterations in medulloblastoma cells |
title_full_unstemmed | Radiation-induced motility alterations in medulloblastoma cells |
title_short | Radiation-induced motility alterations in medulloblastoma cells |
title_sort | radiation-induced motility alterations in medulloblastoma cells |
topic | Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426914/ https://www.ncbi.nlm.nih.gov/pubmed/25736470 http://dx.doi.org/10.1093/jrr/rru120 |
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