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Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons
Relative Biological Effectiveness (RBE), the ratio of doses between radiation modalities to produce the same biological endpoint, is a controversial and important topic in proton therapy. A number of phenomenological models incorporate variable RBE as a function of Linear Energy Transfer (LET), thou...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061037/ https://www.ncbi.nlm.nih.gov/pubmed/35518487 http://dx.doi.org/10.1039/c8ra10168j |
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author | Henthorn, N. T. Warmenhoven, J. W. Sotiropoulos, M. Aitkenhead, A. H. Smith, E. A. K. Ingram, S. P. Kirkby, N. F. Chadwick, A. L. Burnet, N. G. Mackay, R. I. Kirkby, K. J. Merchant, M. J. |
author_facet | Henthorn, N. T. Warmenhoven, J. W. Sotiropoulos, M. Aitkenhead, A. H. Smith, E. A. K. Ingram, S. P. Kirkby, N. F. Chadwick, A. L. Burnet, N. G. Mackay, R. I. Kirkby, K. J. Merchant, M. J. |
author_sort | Henthorn, N. T. |
collection | PubMed |
description | Relative Biological Effectiveness (RBE), the ratio of doses between radiation modalities to produce the same biological endpoint, is a controversial and important topic in proton therapy. A number of phenomenological models incorporate variable RBE as a function of Linear Energy Transfer (LET), though a lack of mechanistic description limits their applicability. In this work we take a different approach, using a track structure model employing fundamental physics and chemistry to make predictions of proton and photon induced DNA damage, the first step in the mechanism of radiation-induced cell death. We apply this model to a proton therapy clinical case showing, for the first time, predictions of DNA damage on a patient treatment plan. Our model predictions are for an idealised cell and are applied to an ependymoma case, at this stage without any cell specific parameters. By comparing to similar predictions for photons, we present a voxel-wise RBE of DNA damage complexity. This RBE of damage complexity shows similar trends to the expected RBE for cell kill, implying that damage complexity is an important factor in DNA repair and therefore biological effect. |
format | Online Article Text |
id | pubmed-9061037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90610372022-05-04 Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons Henthorn, N. T. Warmenhoven, J. W. Sotiropoulos, M. Aitkenhead, A. H. Smith, E. A. K. Ingram, S. P. Kirkby, N. F. Chadwick, A. L. Burnet, N. G. Mackay, R. I. Kirkby, K. J. Merchant, M. J. RSC Adv Chemistry Relative Biological Effectiveness (RBE), the ratio of doses between radiation modalities to produce the same biological endpoint, is a controversial and important topic in proton therapy. A number of phenomenological models incorporate variable RBE as a function of Linear Energy Transfer (LET), though a lack of mechanistic description limits their applicability. In this work we take a different approach, using a track structure model employing fundamental physics and chemistry to make predictions of proton and photon induced DNA damage, the first step in the mechanism of radiation-induced cell death. We apply this model to a proton therapy clinical case showing, for the first time, predictions of DNA damage on a patient treatment plan. Our model predictions are for an idealised cell and are applied to an ependymoma case, at this stage without any cell specific parameters. By comparing to similar predictions for photons, we present a voxel-wise RBE of DNA damage complexity. This RBE of damage complexity shows similar trends to the expected RBE for cell kill, implying that damage complexity is an important factor in DNA repair and therefore biological effect. The Royal Society of Chemistry 2019-02-28 /pmc/articles/PMC9061037/ /pubmed/35518487 http://dx.doi.org/10.1039/c8ra10168j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Henthorn, N. T. Warmenhoven, J. W. Sotiropoulos, M. Aitkenhead, A. H. Smith, E. A. K. Ingram, S. P. Kirkby, N. F. Chadwick, A. L. Burnet, N. G. Mackay, R. I. Kirkby, K. J. Merchant, M. J. Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons |
title | Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons |
title_full | Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons |
title_fullStr | Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons |
title_full_unstemmed | Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons |
title_short | Clinically relevant nanodosimetric simulation of DNA damage complexity from photons and protons |
title_sort | clinically relevant nanodosimetric simulation of dna damage complexity from photons and protons |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061037/ https://www.ncbi.nlm.nih.gov/pubmed/35518487 http://dx.doi.org/10.1039/c8ra10168j |
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