Assessment of DNA damage with an adapted independent reaction time approach implemented in Geant4-DNA for the simulation of diffusion-controlled reactions between radio-induced reactive species and a chromatin fiber.


Journal

Medical physics
ISSN: 2473-4209
Titre abrégé: Med Phys
Pays: United States
ID NLM: 0425746

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 08 07 2020
revised: 06 11 2020
accepted: 10 11 2020
pubmed: 25 11 2020
medline: 15 5 2021
entrez: 24 11 2020
Statut: ppublish

Résumé

Simulation of indirect damage originating from the attack of free radical species produced by ionizing radiation on biological molecules based on the independent pair approximation is investigated in this work. In addition, a new approach, relying on the independent pair approximation that is at the origin of the independent reaction time (IRT) method, is proposed in the chemical stage of Geant4-DNA. This new approach has been designed to respect the current Geant4-DNA chemistry framework while proposing a variant IRT method. Based on the synchronous algorithm, this implementation allows us to access the information concerning the position of radicals and may make it more convenient for biological damage simulations. Estimates of the evolution of free species as well as biological hits in a segment of DNA chromatin fiber in Geant4-DNA were compared for the dynamic time step approach of the step-by-step (SBS) method, currently used in Geant4-DNA, and this newly implemented IRT. Results show a gain in computation time of a factor of 30 for high LET particle tracks with a better than 10% agreement on the number of DNA hits between the value obtained with the IRT method as implemented in this work and the SBS method currently available in Geant4-DNA. Offering in Geant4-DNA more efficient methods for the chemical step based on the IRT method is a task in progress. For the calculation of biological damage, information on the position of chemical species is a crucial point. This can be achieved using the method presented in this paper.

Identifiants

pubmed: 33232522
doi: 10.1002/mp.14612
pmc: PMC7986154
doi:

Substances chimiques

Chromatin 0
DNA 9007-49-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

890-901

Subventions

Organisme : Institut de Radioprotection et de SÛreté Nucléaire (IRSN)

Informations de copyright

© 2020 The Authors. Medical Physics published by Wiley Periodicals LLC on behalf of American Association of Physicists in Medicine.

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Auteurs

Hoang Ngoc Tran (HN)

IRSN, Institut de Radioprotection et de Sûreté Nucléaire, BP17, Fontenay aux Roses, 92262, France.

José Ramos-Méndez (J)

Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, 94115, USA.

Wook-Geun Shin (WG)

Université de Bordeaux, CNRS/IN2P3, UMR5797, Centre d'Études Nucléaires de Bordeaux Gradignan, Gradignan, 33175, France.
Department of Radiation Convergence Engineering, Yonsei University, Wonju, 26493, Korea.

Yann Perrot (Y)

IRSN, Institut de Radioprotection et de Sûreté Nucléaire, BP17, Fontenay aux Roses, 92262, France.

Bruce Faddegon (B)

Department of Radiation Oncology, University of California San Francisco, San Francisco, CA, 94115, USA.

Shogo Okada (S)

KEK, 1-1, Oho, Tsukuba, Ibaraki, 305-0801, Japan.

Mathieu Karamitros (M)

Radiation Laboratory, University of Notre Dame, Notre Dame, In, 46556, USA.

Marie Davídková (M)

Department of Radiation Dosimetry, Nuclear Physics Institute of the CAS, Prague, Czech Republic.

Václav Štěpán (V)

Department of Radiation Dosimetry, Nuclear Physics Institute of the CAS, Prague, Czech Republic.

Sébastien Incerti (S)

Université de Bordeaux, CNRS/IN2P3, UMR5797, Centre d'Études Nucléaires de Bordeaux Gradignan, Gradignan, 33175, France.

Carmen Villagrasa (C)

IRSN, Institut de Radioprotection et de Sûreté Nucléaire, BP17, Fontenay aux Roses, 92262, France.

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Classifications MeSH