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Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells
Although static magnetic fields (SMFs) are used extensively in the occupational and medical fields, few comprehensive studies have investigated their possible genotoxic effect and the findings are controversial. With the advent of magnetic resonance imaging-guided radiation therapy, the potential ef...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951070/ https://www.ncbi.nlm.nih.gov/pubmed/24345558 http://dx.doi.org/10.1093/jrr/rrt107 |
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author | Teodori, Laura Giovanetti, Anna Albertini, Maria Cristina Rocchi, Marco Perniconi, Barbara Valente, Maria Giovanna Coletti, Dario |
author_facet | Teodori, Laura Giovanetti, Anna Albertini, Maria Cristina Rocchi, Marco Perniconi, Barbara Valente, Maria Giovanna Coletti, Dario |
author_sort | Teodori, Laura |
collection | PubMed |
description | Although static magnetic fields (SMFs) are used extensively in the occupational and medical fields, few comprehensive studies have investigated their possible genotoxic effect and the findings are controversial. With the advent of magnetic resonance imaging-guided radiation therapy, the potential effects of SMFs on ionizing radiation (IR) have become increasingly important. In this study we focused on the genotoxic effect of 80 mT SMFs, both alone and in combination with (i.e. preceding or following) X-ray (XR) irradiation, on primary glioblastoma cells in culture. The cells were exposed to: (i) SMFs alone; (ii) XRs alone; (iii) XR, with SMFs applied during recovery; (iv) SMFs both before and after XR irradiation. XR-induced DNA damage was analyzed by Single Cell Gel Electrophoresis assay (comet assay) using statistical tools designed to assess the tail DNA (TD) and tail length (TL) as indicators of DNA fragmentation. Mitochondrial membrane potential, known to be affected by IR, was assessed using the JC-1 mitochondrial probe. Our results showed that exposure of cells to 5 Gy of XR irradiation alone led to extensive DNA damage, which was significantly reduced by post-irradiation exposure to SMFs. The XR-induced loss of mitochondrial membrane potential was to a large extent averted by exposure to SMFs. These data suggest that SMFs modulate DNA damage and/or damage repair, possibly through a mechanism that affects mitochondria. |
format | Online Article Text |
id | pubmed-3951070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39510702014-03-12 Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells Teodori, Laura Giovanetti, Anna Albertini, Maria Cristina Rocchi, Marco Perniconi, Barbara Valente, Maria Giovanna Coletti, Dario J Radiat Res Biology Although static magnetic fields (SMFs) are used extensively in the occupational and medical fields, few comprehensive studies have investigated their possible genotoxic effect and the findings are controversial. With the advent of magnetic resonance imaging-guided radiation therapy, the potential effects of SMFs on ionizing radiation (IR) have become increasingly important. In this study we focused on the genotoxic effect of 80 mT SMFs, both alone and in combination with (i.e. preceding or following) X-ray (XR) irradiation, on primary glioblastoma cells in culture. The cells were exposed to: (i) SMFs alone; (ii) XRs alone; (iii) XR, with SMFs applied during recovery; (iv) SMFs both before and after XR irradiation. XR-induced DNA damage was analyzed by Single Cell Gel Electrophoresis assay (comet assay) using statistical tools designed to assess the tail DNA (TD) and tail length (TL) as indicators of DNA fragmentation. Mitochondrial membrane potential, known to be affected by IR, was assessed using the JC-1 mitochondrial probe. Our results showed that exposure of cells to 5 Gy of XR irradiation alone led to extensive DNA damage, which was significantly reduced by post-irradiation exposure to SMFs. The XR-induced loss of mitochondrial membrane potential was to a large extent averted by exposure to SMFs. These data suggest that SMFs modulate DNA damage and/or damage repair, possibly through a mechanism that affects mitochondria. Oxford University Press 2014-03 2013-12-17 /pmc/articles/PMC3951070/ /pubmed/24345558 http://dx.doi.org/10.1093/jrr/rrt107 Text en © The Author 2013. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), 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 Teodori, Laura Giovanetti, Anna Albertini, Maria Cristina Rocchi, Marco Perniconi, Barbara Valente, Maria Giovanna Coletti, Dario Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells |
title | Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells |
title_full | Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells |
title_fullStr | Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells |
title_full_unstemmed | Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells |
title_short | Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells |
title_sort | static magnetic fields modulate x-ray-induced dna damage in human glioblastoma primary cells |
topic | Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951070/ https://www.ncbi.nlm.nih.gov/pubmed/24345558 http://dx.doi.org/10.1093/jrr/rrt107 |
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