Performance Evaluation for Repair of HSGc-C5 Carcinoma Cell Using Geant4-DNA.

DNA repair Geant4-DNA cell surviving fraction

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 Nov 2021
Historique:
received: 06 07 2021
revised: 30 08 2021
accepted: 07 09 2021
entrez: 10 12 2021
pubmed: 11 12 2021
medline: 11 12 2021
Statut: epublish

Résumé

Track-structure Monte Carlo simulations are useful tools to evaluate initial DNA damage induced by irradiation. In the previous study, we have developed a Gean4-DNA-based application to estimate the cell surviving fraction of V79 cells after irradiation, bridging the gap between the initial DNA damage and the DNA rejoining kinetics by means of the two-lesion kinetics (TLK) model. However, since the DNA repair performance depends on cell line, the same model parameters cannot be used for different cell lines. Thus, we extended the Geant4-DNA application with a TLK model for the evaluation of DNA damage repair performance in HSGc-C5 carcinoma cells which are typically used for evaluating proton/carbon radiation treatment effects. For this evaluation, we also performed experimental measurements for cell surviving fractions and DNA rejoining kinetics of the HSGc-C5 cells irradiated by 70 MeV protons at the cyclotron facility at the National Institutes for Quantum and Radiological Science and Technology (QST). Concerning fast- and slow-DNA rejoining, the TLK model parameters were adequately optimized with the simulated initial DNA damage. The optimized DNA rejoining speeds were reasonably agreed with the experimental DNA rejoining speeds. Using the optimized TLK model, the Geant4-DNA simulation is now able to predict cell survival and DNA-rejoining kinetics for HSGc-C5 cells.

Identifiants

pubmed: 34885155
pii: cancers13236046
doi: 10.3390/cancers13236046
pmc: PMC8656964
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : JSPS KAKENHI
ID : JP20K16840
Organisme : QST President's Strategic Grant
ID : Creative Research

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Auteurs

Dousatsu Sakata (D)

Department of Accelerator and Medical Physics, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Masao Suzuki (M)

Department of Charged Particle Therapy Research, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Ryoichi Hirayama (R)

Department of Charged Particle Therapy Research, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Yasushi Abe (Y)

Department of Accelerator and Medical Physics, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Masayuki Muramatsu (M)

Department of Accelerator and Medical Physics, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Shinji Sato (S)

Department of Accelerator and Medical Physics, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Oleg Belov (O)

Veksler and Baldin Laboratory of High Energy Physics, Joint Institute for Nuclear Research, 141980 Dubna, Russia.
Institute of System Analysis and Management, Dubna State University, 141980 Dubna, Russia.

Ioanna Kyriakou (I)

Medical Physics Laboratory, Medical School, University of Ioannina, 45110 Ioannina, Greece.

Dimitris Emfietzoglou (D)

Medical Physics Laboratory, Medical School, University of Ioannina, 45110 Ioannina, Greece.

Susanna Guatelli (S)

Centre For Medical Radiation Physics, University of Wollongong, Wollongong 2522, Australia.

Sebastien Incerti (S)

Centre d'Études Nucléaires de Bordeaux Gradignan, CNRS/IN2P3, UMR5797, Université de Bordeaux, F-33170 Gradignan, France.

Taku Inaniwa (T)

Department of Accelerator and Medical Physics, Institute for Quantum Medical Science, QST, Chiba 263-8555, Japan.

Classifications MeSH