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Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs
BACKGROUND: Following human radiation exposure in hospital or accidents, dose assessments are of prime importance in radiation accidents. These issues are of continuing importance with respect to socioeconomic policy relating to the industrial and medical uses of ionizing radiation, and also for ris...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513310/ https://www.ncbi.nlm.nih.gov/pubmed/26261821 http://dx.doi.org/10.4103/2277-9175.158025 |
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author | Tavakoli, Mohammad Bagher Kheirollahi, Majid Kiani, Ali Kazemi, Mohammad Javanmard, Shaghayegh Haghjooy Mohebat, Leili |
author_facet | Tavakoli, Mohammad Bagher Kheirollahi, Majid Kiani, Ali Kazemi, Mohammad Javanmard, Shaghayegh Haghjooy Mohebat, Leili |
author_sort | Tavakoli, Mohammad Bagher |
collection | PubMed |
description | BACKGROUND: Following human radiation exposure in hospital or accidents, dose assessments are of prime importance in radiation accidents. These issues are of continuing importance with respect to socioeconomic policy relating to the industrial and medical uses of ionizing radiation, and also for risk assessment among people who are occupationally exposed to low and/or high linear energy transfer (LET) radiation, such as astronauts, pilots, stewardesses, nuclear power plant workers, and victims of radiation accidents. MATERIALS AND METHODS: In this study, an assay for assessing radiation dose based on the induction of apoptosis in human T-lymphocytes was done to examine T-lymphocyte cells isolated from the fresh blood of 16volunteers, cultured and exposed to gamma rays. Radiation-induced apoptosis (RIA) was assessed by flow cytometric identification of cells displaying apoptosis-associated DNA condensation. RESULTS: Dose-response experiments showed that at 2Gy dose level of radiotherapy programs, the RIA frequency was significantly above control. Apoptotic levels significantly depend on the dose of radiation rather than the donor. CONCLUSION: The results demonstrate the potential use of this assay as a biological indicator of radiation toxicity, optimizing patient dose in radiotherapy and biological dosimetry process. |
format | Online Article Text |
id | pubmed-4513310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45133102015-08-10 Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs Tavakoli, Mohammad Bagher Kheirollahi, Majid Kiani, Ali Kazemi, Mohammad Javanmard, Shaghayegh Haghjooy Mohebat, Leili Adv Biomed Res Original Article BACKGROUND: Following human radiation exposure in hospital or accidents, dose assessments are of prime importance in radiation accidents. These issues are of continuing importance with respect to socioeconomic policy relating to the industrial and medical uses of ionizing radiation, and also for risk assessment among people who are occupationally exposed to low and/or high linear energy transfer (LET) radiation, such as astronauts, pilots, stewardesses, nuclear power plant workers, and victims of radiation accidents. MATERIALS AND METHODS: In this study, an assay for assessing radiation dose based on the induction of apoptosis in human T-lymphocytes was done to examine T-lymphocyte cells isolated from the fresh blood of 16volunteers, cultured and exposed to gamma rays. Radiation-induced apoptosis (RIA) was assessed by flow cytometric identification of cells displaying apoptosis-associated DNA condensation. RESULTS: Dose-response experiments showed that at 2Gy dose level of radiotherapy programs, the RIA frequency was significantly above control. Apoptotic levels significantly depend on the dose of radiation rather than the donor. CONCLUSION: The results demonstrate the potential use of this assay as a biological indicator of radiation toxicity, optimizing patient dose in radiotherapy and biological dosimetry process. Medknow Publications & Media Pvt Ltd 2015-06-04 /pmc/articles/PMC4513310/ /pubmed/26261821 http://dx.doi.org/10.4103/2277-9175.158025 Text en Copyright: © 2015 Tavakoli. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Original Article Tavakoli, Mohammad Bagher Kheirollahi, Majid Kiani, Ali Kazemi, Mohammad Javanmard, Shaghayegh Haghjooy Mohebat, Leili Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
title | Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
title_full | Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
title_fullStr | Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
title_full_unstemmed | Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
title_short | Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
title_sort | annexin v fitc conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513310/ https://www.ncbi.nlm.nih.gov/pubmed/26261821 http://dx.doi.org/10.4103/2277-9175.158025 |
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