| Autor: |
Autsavapromporn N; Division of Radiation Oncology, Department of Radiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand., Kobayashi A; Single Cell Radiation Biology Team, National Institutes for Quantum Science and Technology, Chiba 263-8555, Japan., Liu C; Molecular and Cellular Radiation Biology Group, National Institutes for Quantum Science and Technology, Chiba 263-8555, Japan., Duangya A; Division of Radiation Oncology, Department of Radiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand., Oikawa M; Electrostatic Accelerator Operation Section, National Institutes for Quantum Science and Technology, Chiba 263-8555, Japan., Tengku Ahmad TA; Radiation Safety and Health Division, Malaysian Nuclear Agency, Bangi, Kajang 43000, Selangor, Malaysia., Konishi T; Single Cell Radiation Biology Team, National Institutes for Quantum Science and Technology, Chiba 263-8555, Japan. |
| Abstrakt: |
Tumor hypoxia is the most common feature of radioresistance to the radiotherapy (RT) of lung cancer and results in poor clinical outcomes. High-linear energy transfer (LET) radiation is a novel RT technique to overcome this problem. However, a limited number of studies have been elucidated on the underlying mechanism(s) of RIBE and RISBE in cancer cells exposed to high-LET radiation under hypoxia. Here, we developed a new method to investigate the RIBE and RISBE under hypoxia using the SPICE-QST proton microbeams and a layered tissue co-culture system. Normal lung fibroblast (WI-38) and lung cancer (A549) cells were exposed in the range of 06 Gy of proton microbeams, wherein only ~0.04-0.15% of the cells were traversed by protons. Subsequently, primary bystander A549 cells were co-cultured with secondary bystander A549 cells in the presence or absence of a GJIC and NO inhibitor using co-culture systems. Studies show that there are differences in RIBE in A549 and WI-38 primary bystander cells under normoxia and hypoxia. Interestingly, treatment with a GJIC inhibitor showed an increase in the toxicity of primary bystander WI-38 cells but a decrease in A549 cells under hypoxia. Our results also show the induction of RISBE in secondary bystander A549 cells under hypoxia, where GJIC and NO inhibitors reduced the stressful effects on secondary bystander A549 cells. Together, these preliminary results, for the first time, represented the involvement of intercellular communications through GJIC in propagation of RIBE and RISBE in hypoxic cancer cells. |
