Impact of dose-rate on the low-dose hyper-radiosensitivity and induced radioresistance (HRS/IRR) response
Autor: | Jennifer H. Martin, Clément Devic, Michel Diserbo, Juliette Thariat, Charles Thomas, Nicolas Foray, Elke Bräuer-Krisch |
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Přispěvatelé: | Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), European Synchrotron Radiation Facility (ESRF), IRBA, Institut de Recherche Biomédicale des Armées (IRBA), Centre de Lutte contre le Cancer Antoine Lacassagne [Nice] (UNICANCER/CAL), UNICANCER-Université Côte d'Azur (UCA), Thomas, Charles, groupe Foray-équipe Ansiau/Puisieux, Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), Microbeam Radiation Therapy, Unité de Radiothérapie, Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre de Lutte contre le Cancer Antoine Lacassagne [Nice] (UNICANCER/CAL), Université Côte d'Azur (UCA)-UNICANCER-Université Côte d'Azur (UCA)-UNICANCER-Centre de Lutte contre le Cancer, E02, Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université Nice Sophia Antipolis (1965 - 2019) (UNS), UNICANCER-Université Côte d'Azur (UCA)-UNICANCER-Université Côte d'Azur (UCA)-Centre de Lutte contre le Cancer |
Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: |
Clonogenic survival
DNA Repair MESH: DNA Breaks Double-Stranded Radiation Tolerance DSB repair 030218 nuclear medicine & medical imaging 0302 clinical medicine DNA Breaks Double-Stranded MESH: Animals Cobalt Radioisotopes MESH: Cobalt Radioisotopes MESH: DNA Repair MESH: Radiation Tolerance Radiological and Ultrasound Technology Chemistry Low dose 030220 oncology & carcinogenesis Dna breaks Hyper-radiosensitivity (HRS) response MESH: Radiation Dosage MESH: Cell Line Tumor MESH: Rats Colon induced radioresistance (IRR) response tumor cells [SDV.IB.MN]Life Sciences [q-bio]/Bioengineering/Nuclear medicine Radiation Dosage [SDV.IB.MN] Life Sciences [q-bio]/Bioengineering/Nuclear medicine Andrology 03 medical and health sciences MESH: X-Rays Radioresistance Cell Line Tumor Animals Humans Radiology Nuclear Medicine and imaging Radiosensitivity MESH: Colon radiotherapy dose-rate MESH: Humans business.industry X-Rays MESH: Gamma Rays Rats Cell culture Gamma Rays Hyper radiosensitivity Dose rate Nuclear medicine business |
Zdroj: | International Journal of Radiation Biology International Journal of Radiation Biology, 2013, 89 (10), pp.813-22. ⟨10.3109/09553002.2013.800248⟩ International Journal of Radiation Biology, Informa Healthcare, 2013, 89 (10), pp.813-22. ⟨10.3109/09553002.2013.800248⟩ |
ISSN: | 0955-3002 1362-3095 |
DOI: | 10.3109/09553002.2013.800248⟩ |
Popis: | International audience; PURPOSE: To ask whether dose-rate influences low-dose hyper- radiosensitivity and induced radioresistance (HRS/IRR) response in rat colon progressive (PRO) and regressive (REG) cells. METHODS: Clonogenic survival was applied to tumorigenic PRO and non-tumorigenic REG cells irradiated with (60)Co γ-rays at 0.0025-500 mGy.min(-1). Both clonogenic survival and non-homologous end-joining (NHEJ) pathway involved in DNA double-strand breaks (DSB) repair assays were applied to PRO cells irradiated at 25 mGy.min(-1) with 75 kV X-rays only. RESULTS: Irrespective of dose-rates, marked HRS/IRR responses were observed in PRO but not in REG cells. For PRO cells, the doses at which HRS and IRR responses are maximal were dependent on dose-rate; conversely exposure times during which HRS and IRR responses are maximal (t(HRSmax) and t(IRRmax)) were independent of dose-rate. The t(HRSmax) and t(IRRmax) values were 23 ± 5 s and 66 ± 7 s (mean ± standard error of the mean [SEM], n = 7), in agreement with literature data. Repair data show that t(HRSmax) may correspond to exposure time during which NHEJ is deficient while t(IRRmax) may correspond to exposure time during which NHEJ is complete. CONCLUSION: HRS response may be maximal if exposure times are shorter than t(HRSmax) irrespective of dose, dose-rate and cellular model. Potential application of HRS response in radiotherapy is discussed. |
Databáze: | OpenAIRE |
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