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In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells

Intensity-modulated radiation therapy, when used in the clinic, prolongs fraction delivery time. Here we investigated both the in vivoand in vitroradiobiological effects on the A549 cell line, including the effect of different delivery times with the same dose on A549 tumor growth in nude mice. The...

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Autores principales: Jiang, Ling, Xiong, Xiao-Peng, Hu, Chao-Su, Ou, Zhou-Luo, Zhu, Guo-Pei, Ying,, Hong-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589931/
https://www.ncbi.nlm.nih.gov/pubmed/23090953
http://dx.doi.org/10.1093/jrr/rrs093
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author Jiang, Ling
Xiong, Xiao-Peng
Hu, Chao-Su
Ou, Zhou-Luo
Zhu, Guo-Pei
Ying,, Hong-Mei
author_facet Jiang, Ling
Xiong, Xiao-Peng
Hu, Chao-Su
Ou, Zhou-Luo
Zhu, Guo-Pei
Ying,, Hong-Mei
author_sort Jiang, Ling
collection PubMed
description Intensity-modulated radiation therapy, when used in the clinic, prolongs fraction delivery time. Here we investigated both the in vivoand in vitroradiobiological effects on the A549 cell line, including the effect of different delivery times with the same dose on A549 tumor growth in nude mice. The in vitroeffects were studied with clonogenic assays, using linear-quadratic and incomplete repair models to fit the dose-survival curves. Fractionated irradiation of different doses was given at one fraction per day, simulating a clinical dose-time-fractionation pattern. The longer the interval between the exposures, the more cells survived. To investigate the in vivoeffect, we used sixty-four nude mice implanted with A549 cells in the back legs, randomly assigned into eight groups. A 15 Gy radiation dose was divided into different subfractions. The maximum and minimum tumor diameters were recorded to determine tumor growth. Tumor growth was delayed for groups with prolonged delivery time (40 min) compared to the group receiving a single dose of 15 Gy (P< 0.05), and tumors with a 20 min delivery time had delayed growth compared to those with a 40 min delivery time [20′ (7.5 Gy × 2 F) vs 40′ (7.5 Gy × 2 F), P= 0.035; 20′ (3 Gy × 5 F) vs 40′ (3 Gy × 5 F); P= 0.054; 20′ (1.67 Gy × 9 F) vs 40′ (1.67 Gy × 9 F), P= 0.028]. A prolonged delivery time decreased the radiobiological effects, so we strongly recommend keeping the delivery time as short as possible.
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spelling pubmed-35899312013-03-06 In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells Jiang, Ling Xiong, Xiao-Peng Hu, Chao-Su Ou, Zhou-Luo Zhu, Guo-Pei Ying,, Hong-Mei J Radiat Res Biology Intensity-modulated radiation therapy, when used in the clinic, prolongs fraction delivery time. Here we investigated both the in vivoand in vitroradiobiological effects on the A549 cell line, including the effect of different delivery times with the same dose on A549 tumor growth in nude mice. The in vitroeffects were studied with clonogenic assays, using linear-quadratic and incomplete repair models to fit the dose-survival curves. Fractionated irradiation of different doses was given at one fraction per day, simulating a clinical dose-time-fractionation pattern. The longer the interval between the exposures, the more cells survived. To investigate the in vivoeffect, we used sixty-four nude mice implanted with A549 cells in the back legs, randomly assigned into eight groups. A 15 Gy radiation dose was divided into different subfractions. The maximum and minimum tumor diameters were recorded to determine tumor growth. Tumor growth was delayed for groups with prolonged delivery time (40 min) compared to the group receiving a single dose of 15 Gy (P< 0.05), and tumors with a 20 min delivery time had delayed growth compared to those with a 40 min delivery time [20′ (7.5 Gy × 2 F) vs 40′ (7.5 Gy × 2 F), P= 0.035; 20′ (3 Gy × 5 F) vs 40′ (3 Gy × 5 F); P= 0.054; 20′ (1.67 Gy × 9 F) vs 40′ (1.67 Gy × 9 F), P= 0.028]. A prolonged delivery time decreased the radiobiological effects, so we strongly recommend keeping the delivery time as short as possible. Oxford University Press 2013-03 2012-10-22 /pmc/articles/PMC3589931/ /pubmed/23090953 http://dx.doi.org/10.1093/jrr/rrs093 Text en © The Author 2012. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited
spellingShingle Biology
Jiang, Ling
Xiong, Xiao-Peng
Hu, Chao-Su
Ou, Zhou-Luo
Zhu, Guo-Pei
Ying,, Hong-Mei
In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells
title In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells
title_full In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells
title_fullStr In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells
title_full_unstemmed In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells
title_short In vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in A549 cells
title_sort in vitro and in vivo studies on radiobiological effects of prolonged fraction delivery time in a549 cells
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589931/
https://www.ncbi.nlm.nih.gov/pubmed/23090953
http://dx.doi.org/10.1093/jrr/rrs093
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