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DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA
PURPOSE: The aim of this study was to investigate the time- and dose-dependency of DNA double-strand break (DSB) induction and repair in peripheral blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA. METHODS: Blood samples from 16 prostate cancer patients receiving their f...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584247/ https://www.ncbi.nlm.nih.gov/pubmed/31028426 http://dx.doi.org/10.1007/s00259-019-04317-4 |
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author | Schumann, Sarah Scherthan, Harry Lapa, Constantin Serfling, Sebastian Muhtadi, Razan Lassmann, Michael Eberlein, Uta |
author_facet | Schumann, Sarah Scherthan, Harry Lapa, Constantin Serfling, Sebastian Muhtadi, Razan Lassmann, Michael Eberlein, Uta |
author_sort | Schumann, Sarah |
collection | PubMed |
description | PURPOSE: The aim of this study was to investigate the time- and dose-dependency of DNA double-strand break (DSB) induction and repair in peripheral blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA. METHODS: Blood samples from 16 prostate cancer patients receiving their first (177)Lu-PSMA therapy were taken before and at seven time-points (between 1 h and 96 h) after radionuclide administration. Absorbed doses to the blood were calculated using integrated time–activity curves of the blood and the whole-body. For DSB quantification, leucocytes were isolated, fixed in ethanol and immunostained with γ-H2AX and 53BP1 antibodies. Colocalizing foci of both DSB markers were manually counted in a fluorescence microscope. RESULTS: The average number of radiation-induced foci (RIF) per cell increased within the first 4 h after administration, followed by a decrease indicating DNA repair. The number of RIF during the first 2.6 h correlated linearly with the absorbed dose to the blood (R(2) = 0.58), in good agreement with previously published in-vitro data. At late time-points (48 h and 96 h after administration), the number of RIF correlated linearly with the absorbed dose rate (R(2) = 0.56). In most patients, DNA DSBs were repaired effectively. However, in some patients RIF did not disappear completely even 96 h after administration. CONCLUSION: The general pattern of the time- and dose-dependent induction and disappearance of RIF during (177)Lu-PSMA therapy is similar to that of other radionuclide therapies. |
format | Online Article Text |
id | pubmed-6584247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-65842472019-07-05 DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA Schumann, Sarah Scherthan, Harry Lapa, Constantin Serfling, Sebastian Muhtadi, Razan Lassmann, Michael Eberlein, Uta Eur J Nucl Med Mol Imaging Original Article PURPOSE: The aim of this study was to investigate the time- and dose-dependency of DNA double-strand break (DSB) induction and repair in peripheral blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA. METHODS: Blood samples from 16 prostate cancer patients receiving their first (177)Lu-PSMA therapy were taken before and at seven time-points (between 1 h and 96 h) after radionuclide administration. Absorbed doses to the blood were calculated using integrated time–activity curves of the blood and the whole-body. For DSB quantification, leucocytes were isolated, fixed in ethanol and immunostained with γ-H2AX and 53BP1 antibodies. Colocalizing foci of both DSB markers were manually counted in a fluorescence microscope. RESULTS: The average number of radiation-induced foci (RIF) per cell increased within the first 4 h after administration, followed by a decrease indicating DNA repair. The number of RIF during the first 2.6 h correlated linearly with the absorbed dose to the blood (R(2) = 0.58), in good agreement with previously published in-vitro data. At late time-points (48 h and 96 h after administration), the number of RIF correlated linearly with the absorbed dose rate (R(2) = 0.56). In most patients, DNA DSBs were repaired effectively. However, in some patients RIF did not disappear completely even 96 h after administration. CONCLUSION: The general pattern of the time- and dose-dependent induction and disappearance of RIF during (177)Lu-PSMA therapy is similar to that of other radionuclide therapies. Springer Berlin Heidelberg 2019-04-27 2019 /pmc/articles/PMC6584247/ /pubmed/31028426 http://dx.doi.org/10.1007/s00259-019-04317-4 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Schumann, Sarah Scherthan, Harry Lapa, Constantin Serfling, Sebastian Muhtadi, Razan Lassmann, Michael Eberlein, Uta DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA |
title | DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA |
title_full | DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA |
title_fullStr | DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA |
title_full_unstemmed | DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA |
title_short | DNA damage in blood leucocytes of prostate cancer patients during therapy with (177)Lu-PSMA |
title_sort | dna damage in blood leucocytes of prostate cancer patients during therapy with (177)lu-psma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584247/ https://www.ncbi.nlm.nih.gov/pubmed/31028426 http://dx.doi.org/10.1007/s00259-019-04317-4 |
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