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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
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.
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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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