DNA strand break induction of aqueous plasmid DNA exposed to 30 MeV protons at ultra-high dose rate

Author:

Ohsawa Daisuke1,Hiroyama Yota12,Kobayashi Alisa13,Kusumoto Tamon14,Kitamura Hisashi4,Hojo Satoru5,Kodaira Satoshi14,Konishi Teruaki12

Affiliation:

1. Single Cell Radiation Biology Group, National Institutes for Quantum Science and Technology; 4-9-1 Anagawa, Inageku, Chiba, 263-8555, Japan

2. Graduate School of Health Sciences, Hirosaki University, 66-1 Hommachi, Hirosaki-shi, Aomori, 036-8564, Japan

3. Electrostatic Accelerator Operation Section, National Institutes for Quantum Science and Technology, 4-9-1 Anagawa, Inageku, Chiba, 263-8555, Japan

4. Radiation Measurement Research Group, National Institutes for Quantum Science and Technology, 4-9-1 Anagawa, Inageku, Chiba, 263-8555, Japan

5. Cyclotron Operation Section, National Institutes for Quantum Science and Technology, 4-9-1 Anagawa, Inageku, Chiba, 263-8555, Japan

Abstract

Abstract Radiation cancer therapy with ultra-high dose rate exposure, so called FLASH radiotherapy, appears to reduce normal tissue damage without compromising tumor response. The aim of this study was to clarify whether FLASH exposure of proton beam would be effective in reducing the DNA strand break induction. We applied a simple model system, pBR322 plasmid DNA in aqueous 1 × TE solution, where DNA single strand breaks (SSBs) and double strand breaks (DSBs) can be precisely quantified by gel electrophoresis. Plasmid DNA were exposed to 27.5 MeV protons in the conventional dose rate of 0.05 Gy/s (CONV) and ultra-high dose rate of 40 Gy/s (FLASH). With both dose rate, the kinetics of the SSB and DSB induction were proportional to absorbed dose. The SSB induction of FLASH was significantly less than CONV, which were 8.79 ± 0.14 (10−3 SSB per Gy per molecule) and 10.8 ± 0.68 (10−3 SSB per Gy per molecule), respectively. The DSB induction of FLASH was also slightly less than CONV, but difference was not significant. Altogether, 27.5 MeV proton beam at 40 Gy/s reduced SSB and not DSB, thus its effect may not be significant in reducing lethal DNA damage that become apparent in acute radiation effect.

Funder

KAKENHI

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Radiology, Nuclear Medicine and imaging,Radiation

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