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DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223
Irradiation with high linear energy transfer α-emitters, like the clinically used Ra-223 dichloride, severely damages cells and induces complex DNA damage including closely spaced double-strand breaks (DSBs). As the hematopoietic system is an organ-at-risk for the treatment, knowledge about Ra-223-i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797089/ https://www.ncbi.nlm.nih.gov/pubmed/29396412 http://dx.doi.org/10.1038/s41598-018-20364-7 |
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author | Schumann, Sarah Eberlein, Uta Muhtadi, Razan Lassmann, Michael Scherthan, Harry |
author_facet | Schumann, Sarah Eberlein, Uta Muhtadi, Razan Lassmann, Michael Scherthan, Harry |
author_sort | Schumann, Sarah |
collection | PubMed |
description | Irradiation with high linear energy transfer α-emitters, like the clinically used Ra-223 dichloride, severely damages cells and induces complex DNA damage including closely spaced double-strand breaks (DSBs). As the hematopoietic system is an organ-at-risk for the treatment, knowledge about Ra-223-induced DNA damage in blood leukocytes is highly desirable. Therefore, 36 blood samples from six healthy volunteers were exposed ex-vivo (in solution) to different concentrations of Ra-223. Absorbed doses to the blood were calculated assuming local energy deposition of all α- and β-particles of the decay, ranging from 0 to 142 mGy. γ-H2AX + 53BP1 co-staining and analysis was performed in leukocytes isolated from the irradiated blood samples. For DNA damage quantification, leukocyte samples were screened for occurrence of α-induced DNA damage tracks and small γ-H2AX + 53BP1 DSB foci. This revealed a linear relationship between the frequency of α-induced γ-H2AX damage tracks and the absorbed dose to the blood, while the frequency of small γ-H2AX + 53BP1 DSB foci indicative of β-irradiation was similar to baseline values, being in agreement with a negligible β-contribution (3.7%) to the total absorbed dose to the blood. Our calibration curve will contribute to the biodosimetry of Ra-223-treated patients and early after incorporation of α-emitters. |
format | Online Article Text |
id | pubmed-5797089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57970892018-02-12 DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 Schumann, Sarah Eberlein, Uta Muhtadi, Razan Lassmann, Michael Scherthan, Harry Sci Rep Article Irradiation with high linear energy transfer α-emitters, like the clinically used Ra-223 dichloride, severely damages cells and induces complex DNA damage including closely spaced double-strand breaks (DSBs). As the hematopoietic system is an organ-at-risk for the treatment, knowledge about Ra-223-induced DNA damage in blood leukocytes is highly desirable. Therefore, 36 blood samples from six healthy volunteers were exposed ex-vivo (in solution) to different concentrations of Ra-223. Absorbed doses to the blood were calculated assuming local energy deposition of all α- and β-particles of the decay, ranging from 0 to 142 mGy. γ-H2AX + 53BP1 co-staining and analysis was performed in leukocytes isolated from the irradiated blood samples. For DNA damage quantification, leukocyte samples were screened for occurrence of α-induced DNA damage tracks and small γ-H2AX + 53BP1 DSB foci. This revealed a linear relationship between the frequency of α-induced γ-H2AX damage tracks and the absorbed dose to the blood, while the frequency of small γ-H2AX + 53BP1 DSB foci indicative of β-irradiation was similar to baseline values, being in agreement with a negligible β-contribution (3.7%) to the total absorbed dose to the blood. Our calibration curve will contribute to the biodosimetry of Ra-223-treated patients and early after incorporation of α-emitters. Nature Publishing Group UK 2018-02-02 /pmc/articles/PMC5797089/ /pubmed/29396412 http://dx.doi.org/10.1038/s41598-018-20364-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schumann, Sarah Eberlein, Uta Muhtadi, Razan Lassmann, Michael Scherthan, Harry DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 |
title | DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 |
title_full | DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 |
title_fullStr | DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 |
title_full_unstemmed | DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 |
title_short | DNA damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter Ra-223 |
title_sort | dna damage in leukocytes after internal ex-vivo irradiation of blood with the α-emitter ra-223 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5797089/ https://www.ncbi.nlm.nih.gov/pubmed/29396412 http://dx.doi.org/10.1038/s41598-018-20364-7 |
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