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DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate
Radiation cancer therapy with ultra-high dose rate exposure, so called FLASH radiotherapy, appears to reduce normal tissue damage without compromising tumor response. The aim of this study was to clarify whether FLASH exposure of proton beam would be effective in reducing the DNA strand break induct...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944314/ https://www.ncbi.nlm.nih.gov/pubmed/34952540 http://dx.doi.org/10.1093/jrr/rrab114 |
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author | Ohsawa, Daisuke Hiroyama, Yota Kobayashi, Alisa Kusumoto, Tamon Kitamura, Hisashi Hojo, Satoru Kodaira, Satoshi Konishi, Teruaki |
author_facet | Ohsawa, Daisuke Hiroyama, Yota Kobayashi, Alisa Kusumoto, Tamon Kitamura, Hisashi Hojo, Satoru Kodaira, Satoshi Konishi, Teruaki |
author_sort | Ohsawa, Daisuke |
collection | PubMed |
description | Radiation cancer therapy with ultra-high dose rate exposure, so called FLASH radiotherapy, appears to reduce normal tissue damage without compromising tumor response. The aim of this study was to clarify whether FLASH exposure of proton beam would be effective in reducing the DNA strand break induction. We applied a simple model system, pBR322 plasmid DNA in aqueous 1 × TE solution, where DNA single strand breaks (SSBs) and double strand breaks (DSBs) can be precisely quantified by gel electrophoresis. Plasmid DNA were exposed to 27.5 MeV protons in the conventional dose rate of 0.05 Gy/s (CONV) and ultra-high dose rate of 40 Gy/s (FLASH). With both dose rate, the kinetics of the SSB and DSB induction were proportional to absorbed dose. The SSB induction of FLASH was significantly less than CONV, which were 8.79 ± 0.14 (10(−3) SSB per Gy per molecule) and 10.8 ± 0.68 (10(−3) SSB per Gy per molecule), respectively. The DSB induction of FLASH was also slightly less than CONV, but difference was not significant. Altogether, 27.5 MeV proton beam at 40 Gy/s reduced SSB and not DSB, thus its effect may not be significant in reducing lethal DNA damage that become apparent in acute radiation effect. |
format | Online Article Text |
id | pubmed-8944314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89443142022-03-28 DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate Ohsawa, Daisuke Hiroyama, Yota Kobayashi, Alisa Kusumoto, Tamon Kitamura, Hisashi Hojo, Satoru Kodaira, Satoshi Konishi, Teruaki J Radiat Res Fundamental Radiation Science Radiation cancer therapy with ultra-high dose rate exposure, so called FLASH radiotherapy, appears to reduce normal tissue damage without compromising tumor response. The aim of this study was to clarify whether FLASH exposure of proton beam would be effective in reducing the DNA strand break induction. We applied a simple model system, pBR322 plasmid DNA in aqueous 1 × TE solution, where DNA single strand breaks (SSBs) and double strand breaks (DSBs) can be precisely quantified by gel electrophoresis. Plasmid DNA were exposed to 27.5 MeV protons in the conventional dose rate of 0.05 Gy/s (CONV) and ultra-high dose rate of 40 Gy/s (FLASH). With both dose rate, the kinetics of the SSB and DSB induction were proportional to absorbed dose. The SSB induction of FLASH was significantly less than CONV, which were 8.79 ± 0.14 (10(−3) SSB per Gy per molecule) and 10.8 ± 0.68 (10(−3) SSB per Gy per molecule), respectively. The DSB induction of FLASH was also slightly less than CONV, but difference was not significant. Altogether, 27.5 MeV proton beam at 40 Gy/s reduced SSB and not DSB, thus its effect may not be significant in reducing lethal DNA damage that become apparent in acute radiation effect. Oxford University Press 2021-12-25 /pmc/articles/PMC8944314/ /pubmed/34952540 http://dx.doi.org/10.1093/jrr/rrab114 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. https://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 (https://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 | Fundamental Radiation Science Ohsawa, Daisuke Hiroyama, Yota Kobayashi, Alisa Kusumoto, Tamon Kitamura, Hisashi Hojo, Satoru Kodaira, Satoshi Konishi, Teruaki DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate |
title | DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate |
title_full | DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate |
title_fullStr | DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate |
title_full_unstemmed | DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate |
title_short | DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate |
title_sort | dna strand break induction of aqueous plasmid dna exposed to 30 mev protons at ultra-high dose rate |
topic | Fundamental Radiation Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8944314/ https://www.ncbi.nlm.nih.gov/pubmed/34952540 http://dx.doi.org/10.1093/jrr/rrab114 |
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