Gold-Nanoparticles-Enhanced Production of Reactive Oxygen Species in Cells at Spread-Out Bragg Peak under Proton Beam Radiation.
Chang-Yun LoShiao-Wen TsaiHuan NiuFang-Hsin ChenHsiao-Chien HwangTsi-Chian ChaoIng-Tsung HsiaoJiunn-Woei LiawPublished in: ACS omega (2023)
This study investigates the radiobiological effects of gold nanoparticles (GNPs) as radiosensitizers for proton beam therapy (PBT). Specifically, we explore the enhanced production of reactive oxygen species (ROS) in GNP-loaded tumor cells irradiated by a 230 MeV proton beam in a spread-out Bragg peak (SOBP) zone obtained by a passive scattering system. Our findings indicate that the radiosensitization enhancement factor is 1.24 at 30% cell survival fraction, 8 days after 6 Gy proton beam irradiation. Since protons deposit the majority of their energy at the SOBP region and interact with GNPs to induce more ejected electrons from the high-Z GNPs, these ejected electrons then react with water molecules to produce excessive ROS that can damage cellular organelles. Laser scanning confocal microscopy reveals the excessive ROS induced inside the GNP-loaded cells immediately after proton irradiation. Furthermore, the damage to cytoskeletons and mitochondrial dysfunction in GNP-loaded cells caused by the induced ROS becomes significantly severe, 48 h after proton irradiation. Our biological evidence suggests that the cytotoxicity of GNP-enhanced ROS production has the potential to increase the tumoricidal efficacy of PBT.
Keyphrases
- reactive oxygen species
- gold nanoparticles
- induced apoptosis
- cell death
- cell cycle arrest
- dna damage
- drug delivery
- oxidative stress
- high glucose
- endoplasmic reticulum stress
- early onset
- smoking cessation
- reduced graphene oxide
- physical activity
- bone marrow
- endothelial cells
- monte carlo
- weight loss
- radiation therapy
- cell therapy