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Clustered DNA Damage Patterns after Proton Therapy Beam Irradiation Using Plasmid DNA
- 1.0566892 - ÚJF 2023 RIV CH eng J - Journal Article
Souli, M. P. - Nikitaki, Z. - Puchalská, M. - Pachnerová Brabcová, Kateřina - Spyratou, E. - Kote, P. - Efstathopoulos, E. P. - Hada, M. - Georgakilas, A. G. - Sihver, Lembit
Clustered DNA Damage Patterns after Proton Therapy Beam Irradiation Using Plasmid DNA.
International Journal of Molecular Sciences. Roč. 23, č. 24 (2022), č. článku 15606. E-ISSN 1422-0067
Institutional support: RVO:61389005
Keywords : proton therapy beam * clustered DNA damage * linear energy transfer (LET) * Agarose Gel Electrophoresis (AGE) * Atomic Force Microscopy (AFM) * damage biomarkers * scavenging capacity * biodosimetry
OECD category: Biochemistry and molecular biology
Impact factor: 5.6, year: 2022
Method of publishing: Open access
https://doi.org/10.3390/ijms232415606
Modeling ionizing radiation interaction with biological matter is a major scientific challenge, especially for protons that are nowadays widely used in cancer treatment. That presupposes a sound understanding of the mechanisms that take place from the early events of the induction of DNA damage. Herein, we present results of irradiation-induced complex DNA damage measurements using plasmid pBR322 along a typical Proton Treatment Plan at the MedAustron proton and carbon beam therapy facility (energy 137-198 MeV and Linear Energy Transfer (LET) range 1-9 keV/mu m), by means of Agarose Gel Electrophoresis and DNA fragmentation using Atomic Force Microscopy (AFM). The induction rate Mbp(-1) Gy(-1) for each type of damage, single strand breaks (SSBs), double-strand breaks (DSBs), base lesions and non-DSB clusters was measured after irradiations in solutions with varying scavenging capacity containing 2-amino-2-(hydroxymethyl)propane-1,3-diol (Tris) and coumarin-3-carboxylic acid (C3CA) as scavengers. Our combined results reveal the determining role of LET and Reactive Oxygen Species (ROS) in DNA fragmentation. Furthermore, AFM used to measure apparent DNA lengths provided us with insights into the role of increasing LET in the induction of highly complex DNA damage.
Permanent Link: https://hdl.handle.net/11104/0338159
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