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(99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency
(99m)Tc is the standard radionuclide used for nuclear medicine imaging. In addition to gamma irradiation, (99m)Tc emits low-energy Auger and conversion electrons that deposit their energy within nanometers of the decay site. To study the potential for DNA damage, direct DNA binding is required. Plas...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123991/ https://www.ncbi.nlm.nih.gov/pubmed/25098953 http://dx.doi.org/10.1371/journal.pone.0104653 |
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author | Kotzerke, Joerg Punzet, Robert Runge, Roswitha Ferl, Sandra Oehme, Liane Wunderlich, Gerd Freudenberg, Robert |
author_facet | Kotzerke, Joerg Punzet, Robert Runge, Roswitha Ferl, Sandra Oehme, Liane Wunderlich, Gerd Freudenberg, Robert |
author_sort | Kotzerke, Joerg |
collection | PubMed |
description | (99m)Tc is the standard radionuclide used for nuclear medicine imaging. In addition to gamma irradiation, (99m)Tc emits low-energy Auger and conversion electrons that deposit their energy within nanometers of the decay site. To study the potential for DNA damage, direct DNA binding is required. Plasmid DNA enables the investigation of the unprotected interactions between molecules and DNA that result in single-strand breaks (SSBs) or double-strand breaks (DSBs); the resulting DNA fragments can be separated by gel electrophoresis and quantified by fluorescent staining. This study aimed to compare the plasmid DNA damage potential of a (99m)Tc-labeled HYNIC-DAPI compound with that of (99m)Tc pertechnetate ((99m)TcO(4) (−)). pUC19 plasmid DNA was irradiated for 2 or 24 hours. Direct and radical-induced DNA damage were evaluated in the presence or absence of the radical scavenger DMSO. For both compounds, an increase in applied activity enhanced plasmid DNA damage, which was evidenced by an increase in the open circular and linear DNA fractions and a reduction in the supercoiled DNA fraction. The number of SSBs elicited by (99m)Tc-HYNIC-DAPI (1.03) was twice that caused by (99m)TcO(4) (−) (0.51), and the number of DSBs increased fivefold in the (99m)Tc-HYNIC-DAPI-treated sample compared with the (99m)TcO(4) (−) treated sample (0.02 to 0.10). In the presence of DMSO, the numbers of SSBs and DSBs decreased to 0.03 and 0.00, respectively, in the (99m)TcO(4) (–) treated samples, whereas the numbers of SSBs and DSBs were slightly reduced to 0.95 and 0.06, respectively, in the (99m)Tc-HYNIC-DAPI-treated samples. These results indicated that (99m)Tc-HYNIC-DAPI induced SSBs and DSBs via a direct interaction of the (99m)Tc-labeled compound with DNA. In contrast to these results, (99m)TcO(4) (−) induced SSBs via radical formation, and DSBs were formed by two nearby SSBs. The biological effectiveness of (99m)Tc-HYNIC-DAPI increased by approximately 4-fold in terms of inducing SSBs and by approximately 10-fold in terms of inducing DSBs. |
format | Online Article Text |
id | pubmed-4123991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41239912014-08-12 (99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency Kotzerke, Joerg Punzet, Robert Runge, Roswitha Ferl, Sandra Oehme, Liane Wunderlich, Gerd Freudenberg, Robert PLoS One Research Article (99m)Tc is the standard radionuclide used for nuclear medicine imaging. In addition to gamma irradiation, (99m)Tc emits low-energy Auger and conversion electrons that deposit their energy within nanometers of the decay site. To study the potential for DNA damage, direct DNA binding is required. Plasmid DNA enables the investigation of the unprotected interactions between molecules and DNA that result in single-strand breaks (SSBs) or double-strand breaks (DSBs); the resulting DNA fragments can be separated by gel electrophoresis and quantified by fluorescent staining. This study aimed to compare the plasmid DNA damage potential of a (99m)Tc-labeled HYNIC-DAPI compound with that of (99m)Tc pertechnetate ((99m)TcO(4) (−)). pUC19 plasmid DNA was irradiated for 2 or 24 hours. Direct and radical-induced DNA damage were evaluated in the presence or absence of the radical scavenger DMSO. For both compounds, an increase in applied activity enhanced plasmid DNA damage, which was evidenced by an increase in the open circular and linear DNA fractions and a reduction in the supercoiled DNA fraction. The number of SSBs elicited by (99m)Tc-HYNIC-DAPI (1.03) was twice that caused by (99m)TcO(4) (−) (0.51), and the number of DSBs increased fivefold in the (99m)Tc-HYNIC-DAPI-treated sample compared with the (99m)TcO(4) (−) treated sample (0.02 to 0.10). In the presence of DMSO, the numbers of SSBs and DSBs decreased to 0.03 and 0.00, respectively, in the (99m)TcO(4) (–) treated samples, whereas the numbers of SSBs and DSBs were slightly reduced to 0.95 and 0.06, respectively, in the (99m)Tc-HYNIC-DAPI-treated samples. These results indicated that (99m)Tc-HYNIC-DAPI induced SSBs and DSBs via a direct interaction of the (99m)Tc-labeled compound with DNA. In contrast to these results, (99m)TcO(4) (−) induced SSBs via radical formation, and DSBs were formed by two nearby SSBs. The biological effectiveness of (99m)Tc-HYNIC-DAPI increased by approximately 4-fold in terms of inducing SSBs and by approximately 10-fold in terms of inducing DSBs. Public Library of Science 2014-08-06 /pmc/articles/PMC4123991/ /pubmed/25098953 http://dx.doi.org/10.1371/journal.pone.0104653 Text en © 2014 Kotzerke et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Kotzerke, Joerg Punzet, Robert Runge, Roswitha Ferl, Sandra Oehme, Liane Wunderlich, Gerd Freudenberg, Robert (99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency |
title |
(99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency |
title_full |
(99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency |
title_fullStr |
(99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency |
title_full_unstemmed |
(99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency |
title_short |
(99m)Tc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency |
title_sort | (99m)tc-labeled hynic-dapi causes plasmid dna damage with high efficiency |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123991/ https://www.ncbi.nlm.nih.gov/pubmed/25098953 http://dx.doi.org/10.1371/journal.pone.0104653 |
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