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Impact of time interval and dose rate on cell survival following low-dose fractionated exposures

Enhanced cell lethality, also known as hyper-radiosensitivity, has been reported at low doses of radiation (≤0.5 Gy) in various cell lines, and is expected to be an effective cancer therapy. We conducted this study to examine the impact of time interval and dose rate of low-dose fractionated exposur...

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Autores principales: Terashima, Shingo, Hosokawa, Yoichiro, Tsuruga, Eichi, Mariya, Yasushi, Nakamura, Toshiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710595/
https://www.ncbi.nlm.nih.gov/pubmed/28595296
http://dx.doi.org/10.1093/jrr/rrx025
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author Terashima, Shingo
Hosokawa, Yoichiro
Tsuruga, Eichi
Mariya, Yasushi
Nakamura, Toshiya
author_facet Terashima, Shingo
Hosokawa, Yoichiro
Tsuruga, Eichi
Mariya, Yasushi
Nakamura, Toshiya
author_sort Terashima, Shingo
collection PubMed
description Enhanced cell lethality, also known as hyper-radiosensitivity, has been reported at low doses of radiation (≤0.5 Gy) in various cell lines, and is expected to be an effective cancer therapy. We conducted this study to examine the impact of time interval and dose rate of low-dose fractionated exposures with a short time interval. We evaluated the cell-survival rates of V79 and A549 cells using clonogenic assays. We performed fractionated exposures in unit doses of 0.25, 0.5, 1.0 and 2.0 Gy. We exposed the cells to 2 Gy of X-rays (i) at dose-rates of 1.0, 1.5 and 2.0 Gy/min at 1-min intervals and (ii) at a dose-rate of 2.0 Gy/min at 10-s, 1-min and 3-min intervals by fractionated exposures. Apoptosis and cell cycle analyses were also evaluated in the fractionated exposures (unit dose 0.25 Gy) and compared with single exposures by using flow cytometry. Both cell-type survival rates with fractionated exposures (unit dose 0.25 Gy) with short time intervals were markedly lower than those for single exposures delivering the same dose. When the dose rates were lower, the cytotoxic effect decreased compared with exposure to a dose-rate of 2.0 Gy/min. On the other hand, levels of apoptosis and cell cycle distribution were not significantly different between low-dose fractionated exposures and single exposures in either cell line. These results indicate that a stronger cytotoxic effect was induced with low-dose fractionated exposures with a short time interval for a given dose due to the hyper-radiosensitivity phenomenon, suggesting that dose rates are important for effective low-dose fractionated exposures.
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spelling pubmed-57105952017-12-07 Impact of time interval and dose rate on cell survival following low-dose fractionated exposures Terashima, Shingo Hosokawa, Yoichiro Tsuruga, Eichi Mariya, Yasushi Nakamura, Toshiya J Radiat Res Biology Enhanced cell lethality, also known as hyper-radiosensitivity, has been reported at low doses of radiation (≤0.5 Gy) in various cell lines, and is expected to be an effective cancer therapy. We conducted this study to examine the impact of time interval and dose rate of low-dose fractionated exposures with a short time interval. We evaluated the cell-survival rates of V79 and A549 cells using clonogenic assays. We performed fractionated exposures in unit doses of 0.25, 0.5, 1.0 and 2.0 Gy. We exposed the cells to 2 Gy of X-rays (i) at dose-rates of 1.0, 1.5 and 2.0 Gy/min at 1-min intervals and (ii) at a dose-rate of 2.0 Gy/min at 10-s, 1-min and 3-min intervals by fractionated exposures. Apoptosis and cell cycle analyses were also evaluated in the fractionated exposures (unit dose 0.25 Gy) and compared with single exposures by using flow cytometry. Both cell-type survival rates with fractionated exposures (unit dose 0.25 Gy) with short time intervals were markedly lower than those for single exposures delivering the same dose. When the dose rates were lower, the cytotoxic effect decreased compared with exposure to a dose-rate of 2.0 Gy/min. On the other hand, levels of apoptosis and cell cycle distribution were not significantly different between low-dose fractionated exposures and single exposures in either cell line. These results indicate that a stronger cytotoxic effect was induced with low-dose fractionated exposures with a short time interval for a given dose due to the hyper-radiosensitivity phenomenon, suggesting that dose rates are important for effective low-dose fractionated exposures. Oxford University Press 2017-11 2017-06-08 /pmc/articles/PMC5710595/ /pubmed/28595296 http://dx.doi.org/10.1093/jrr/rrx025 Text en © The Author 2017. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Biology
Terashima, Shingo
Hosokawa, Yoichiro
Tsuruga, Eichi
Mariya, Yasushi
Nakamura, Toshiya
Impact of time interval and dose rate on cell survival following low-dose fractionated exposures
title Impact of time interval and dose rate on cell survival following low-dose fractionated exposures
title_full Impact of time interval and dose rate on cell survival following low-dose fractionated exposures
title_fullStr Impact of time interval and dose rate on cell survival following low-dose fractionated exposures
title_full_unstemmed Impact of time interval and dose rate on cell survival following low-dose fractionated exposures
title_short Impact of time interval and dose rate on cell survival following low-dose fractionated exposures
title_sort impact of time interval and dose rate on cell survival following low-dose fractionated exposures
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710595/
https://www.ncbi.nlm.nih.gov/pubmed/28595296
http://dx.doi.org/10.1093/jrr/rrx025
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