Abstract
Radiation affects several cellular and molecular processes, including double strand breakage and modifications of sugar moieties and bases. In outer space, protons are the primary radiation source that poses a range of potential health risks to astronauts. On the other hand, the use of proton irradiation for tumor radiation therapy is increasing, as it largely spares healthy tissues while killing tumor tissues. Although radiation-related research has been conducted extensively, the molecular toxicology and cellular mechanisms affected by proton irradiation remain poorly understood. Therefore, in this study, we irradiated rat lung epithelial cells with different doses of protons and investigated their effects on cell proliferation and death. Our data show an inhibition of cell proliferation in proton-irradiated cells with a significant dose-dependent activation and repression of reactive oxygen species and antioxidants glutathione and superoxide dismutase, respectively, compared with control cells. In addition, the activities of apoptosis-related genes such as caspase-3 and -8 were induced in a dose-dependent manner with corresponding increased levels of DNA fragmentation in proton-irradiated cells compared with control cells. Together, our results show that proton irradiation alters oxidant and antioxidant levels in cells to activate the apoptotic pathway for cell death.
Highlights
The mechanism by which radiation causes damage to human tissue is by ionization of atoms
We observed an increased level of reactive oxygen species (ROS) and lipid peroxidation (LPO), followed by inhibition of antioxidants glutathione (GSH) and superoxide dismutase (SOD) in proton-irradiated cells compared with control cells
At hospital-based proton facilities, a dose of 1.8 –2 cobalt Gy eq is often used per fraction, with one fraction delivered per day over a period of 5 days/week for 5–7 weeks, depending on the type and location of the tumor as well as other considerations
Summary
The mechanism by which radiation causes damage to human tissue is by ionization of atoms. The activities of apoptosis-related genes such as caspase-3 and -8 were induced in a dose-dependent manner with corresponding increased levels of DNA fragmentation in proton-irradiated cells compared with control cells.
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