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DOI 10.1016/j.bbrc.2024.149500

Медицинская библиотека · Biochemical and biophysical research communications · 2024

The contribution of high-LET track to DNA damage formation and cell death for Monoenergy and SOBP carbon ion irradiation.

Chailapakul Piyawan, Maloney Olivia, Hirakawa Hirokazu, Fujimori Akira, Kitamura Hisashi, Kato Takamitsu A

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Carbon ion radiotherapy (CIRT) is a heavy ion charge particle therapy with 29 years of prominent use. Despite advantages like high relative biological effectiveness (RBE), improved quality of life, and reduced treatment time, challenges persist, especially regarding heavy nuclear fragments. Our research addresses these challenges in horizontal irradiation, aiming to comprehend Monoenergetic and Spread-Out Bragg peak (SOBP) carbon ion beam trajectories using cell survival analysis and visualizing biological effects through DNA damage (γ-H2AX). This reveals repair-related protein foci near the Bragg peak. CR-39, a plastic nuclear track detector, was explored to understand high-linear energy transfer (LET) tracks and radiation quality near the Bragg peak. Findings unveil high-LET DNA damage signatures through aligned γ-H2AX foci, correlating with LET values in SOBP. CR-39 visualized high-LET particle exposure, indicating comet-type etch-pits at the Bragg peak and suggesting carbon ion fragmentation. Unexpectedly, dot-type etch-pits in irradiated and post-Bragg peak regions indicated high-LET neutron production. This investigation highlights the intricate interplay of carbon ion beams, stressing the importance of understanding LET variations, DNA damage patterns, and undesired secondary exposure.

Для цитирования: Chailapakul Piyawan, Maloney Olivia, Hirakawa Hirokazu, Fujimori Akira, Kitamura Hisashi, Kato Takamitsu A. The contribution of high-LET track to DNA damage formation and cell death for Monoenergy and SOBP carbon ion irradiation.. Biochemical and biophysical research communications. 2024. DOI: 10.1016/j.bbrc.2024.149500.

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