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High-LET radiation induces large amounts of rapidly-repaired sublethal damage

There is agreement that high-LET radiation has a high Relative Biological Effectiveness (RBE) when delivered as a single treatment, but how it interacts with radiations of different qualities, such as X-rays, is less clear. We sought to clarify these effects by quantifying and modelling responses to...

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Autores principales: Guerra Liberal, Francisco D. C., Thompson, Shannon J., Prise, Kevin M., McMahon, Stephen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336062/
https://www.ncbi.nlm.nih.gov/pubmed/37433844
http://dx.doi.org/10.1038/s41598-023-38295-3
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author Guerra Liberal, Francisco D. C.
Thompson, Shannon J.
Prise, Kevin M.
McMahon, Stephen J.
author_facet Guerra Liberal, Francisco D. C.
Thompson, Shannon J.
Prise, Kevin M.
McMahon, Stephen J.
author_sort Guerra Liberal, Francisco D. C.
collection PubMed
description There is agreement that high-LET radiation has a high Relative Biological Effectiveness (RBE) when delivered as a single treatment, but how it interacts with radiations of different qualities, such as X-rays, is less clear. We sought to clarify these effects by quantifying and modelling responses to X-ray and alpha particle combinations. Cells were exposed to X-rays, alpha particles, or combinations, with different doses and temporal separations. DNA damage was assessed by 53BP1 immunofluorescence, and radiosensitivity assessed using the clonogenic assay. Mechanistic models were then applied to understand trends in repair and survival. 53BP1 foci yields were significantly reduced in alpha particle exposures compared to X-rays, but these foci were slow to repair. Although alpha particles alone showed no inter-track interactions, substantial interactions were seen between X-rays and alpha particles. Mechanistic modelling suggested that sublethal damage (SLD) repair was independent of radiation quality, but that alpha particles generated substantially more sublethal damage than a similar dose of X-rays, [Formula: see text] . This high RBE may lead to unexpected synergies for combinations of different radiation qualities which must be taken into account in treatment design, and the rapid repair of this damage may impact on mechanistic modelling of radiation responses to high LETs.
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spelling pubmed-103360622023-07-13 High-LET radiation induces large amounts of rapidly-repaired sublethal damage Guerra Liberal, Francisco D. C. Thompson, Shannon J. Prise, Kevin M. McMahon, Stephen J. Sci Rep Article There is agreement that high-LET radiation has a high Relative Biological Effectiveness (RBE) when delivered as a single treatment, but how it interacts with radiations of different qualities, such as X-rays, is less clear. We sought to clarify these effects by quantifying and modelling responses to X-ray and alpha particle combinations. Cells were exposed to X-rays, alpha particles, or combinations, with different doses and temporal separations. DNA damage was assessed by 53BP1 immunofluorescence, and radiosensitivity assessed using the clonogenic assay. Mechanistic models were then applied to understand trends in repair and survival. 53BP1 foci yields were significantly reduced in alpha particle exposures compared to X-rays, but these foci were slow to repair. Although alpha particles alone showed no inter-track interactions, substantial interactions were seen between X-rays and alpha particles. Mechanistic modelling suggested that sublethal damage (SLD) repair was independent of radiation quality, but that alpha particles generated substantially more sublethal damage than a similar dose of X-rays, [Formula: see text] . This high RBE may lead to unexpected synergies for combinations of different radiation qualities which must be taken into account in treatment design, and the rapid repair of this damage may impact on mechanistic modelling of radiation responses to high LETs. Nature Publishing Group UK 2023-07-11 /pmc/articles/PMC10336062/ /pubmed/37433844 http://dx.doi.org/10.1038/s41598-023-38295-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Guerra Liberal, Francisco D. C.
Thompson, Shannon J.
Prise, Kevin M.
McMahon, Stephen J.
High-LET radiation induces large amounts of rapidly-repaired sublethal damage
title High-LET radiation induces large amounts of rapidly-repaired sublethal damage
title_full High-LET radiation induces large amounts of rapidly-repaired sublethal damage
title_fullStr High-LET radiation induces large amounts of rapidly-repaired sublethal damage
title_full_unstemmed High-LET radiation induces large amounts of rapidly-repaired sublethal damage
title_short High-LET radiation induces large amounts of rapidly-repaired sublethal damage
title_sort high-let radiation induces large amounts of rapidly-repaired sublethal damage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336062/
https://www.ncbi.nlm.nih.gov/pubmed/37433844
http://dx.doi.org/10.1038/s41598-023-38295-3
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