Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation

The aim of this study was to investigate impact of exogenous nitric oxide (NO) on generation of different types of DNA damages, their transformation, and specificity of DNA repair in cells treated with ionizing radiation (IR). Methods: levels of single-strand and double-strand breaks assessed in per...

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Опубліковано в: :Experimental Oncology
Дата:2013
Автори: Mikhailenko, V.M., Muzalov, I.I.
Формат: Стаття
Мова:English
Опубліковано: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2013
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Онлайн доступ:https://nasplib.isofts.kiev.ua/handle/123456789/145268
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Цитувати:Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation / V.M. Mikhailenko, I.I. Muzalov // Experimental Oncology. — 2013. — Т. 35, № 4. — С. 318-324. — Бібліогр.: 43 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
id nasplib_isofts_kiev_ua-123456789-145268
record_format dspace
spelling Mikhailenko, V.M.
Muzalov, I.I.
2019-01-20T08:33:24Z
2019-01-20T08:33:24Z
2013
Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation / V.M. Mikhailenko, I.I. Muzalov // Experimental Oncology. — 2013. — Т. 35, № 4. — С. 318-324. — Бібліогр.: 43 назв. — англ.
1812-9269
https://nasplib.isofts.kiev.ua/handle/123456789/145268
The aim of this study was to investigate impact of exogenous nitric oxide (NO) on generation of different types of DNA damages, their transformation, and specificity of DNA repair in cells treated with ionizing radiation (IR). Methods: levels of single-strand and double-strand breaks assessed in peripheral blood lymphocytes (PBL) isolated from healthy humans and treated in vitro with NO donor — S-nitrosoglutathione (GSNO) and IR. The rate of DNA repair estimated after 30 and 60 min of PBL treatment. The visualization and measuring the number of prompt and delayed DNA damages, including strand breaks, apurinic and thermolabile sites performed with single-cell gel electrophoresis. Results: IR caused dose-dependent generation of single strand breaks (SSBs), double strand breaks (DSBs), and heat-labile sites (HLS) in cell DNA. However, particularly destructive was combined treatment IR with GSNO as NO donor that leads to a significant increase of DNA damage and a dose-dependent inhibition of the DNA repair rate. Obtained data proofs the ability of NO to inhibit fast and slow stages of SSBs, DSBs, and HLS repair resulting in significant growth of genotoxic effect. DNA breaks generation from HLS is able to affect DSBs yields especially in cells with altered DNA repair. The process of DNA repair of delayed DSBs formed from HLS was quite different from removal of DNA damages occurring immediately after treatment and was characterized by IR dose dependent inhibition of DNA repair. Conclusion: High level of DNA strand breaks, that are generated after the combined treatment with NO and IR, are accumulated for quite a long time after exposure due to altered DNA repair, indicating the development of genetic instability and increase of carcinogenic risk for organism exposed to combination of harmful environmental factors.
en
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
Experimental Oncology
Arrticles not related to special issue topics
Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
Article
published earlier
institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
collection DSpace DC
title Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
spellingShingle Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
Mikhailenko, V.M.
Muzalov, I.I.
Arrticles not related to special issue topics
title_short Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
title_full Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
title_fullStr Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
title_full_unstemmed Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation
title_sort exogenous nitric oxide potentiate dna damage and alter dna repair in cells exposed to ionising radiation
author Mikhailenko, V.M.
Muzalov, I.I.
author_facet Mikhailenko, V.M.
Muzalov, I.I.
topic Arrticles not related to special issue topics
topic_facet Arrticles not related to special issue topics
publishDate 2013
language English
container_title Experimental Oncology
publisher Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
format Article
description The aim of this study was to investigate impact of exogenous nitric oxide (NO) on generation of different types of DNA damages, their transformation, and specificity of DNA repair in cells treated with ionizing radiation (IR). Methods: levels of single-strand and double-strand breaks assessed in peripheral blood lymphocytes (PBL) isolated from healthy humans and treated in vitro with NO donor — S-nitrosoglutathione (GSNO) and IR. The rate of DNA repair estimated after 30 and 60 min of PBL treatment. The visualization and measuring the number of prompt and delayed DNA damages, including strand breaks, apurinic and thermolabile sites performed with single-cell gel electrophoresis. Results: IR caused dose-dependent generation of single strand breaks (SSBs), double strand breaks (DSBs), and heat-labile sites (HLS) in cell DNA. However, particularly destructive was combined treatment IR with GSNO as NO donor that leads to a significant increase of DNA damage and a dose-dependent inhibition of the DNA repair rate. Obtained data proofs the ability of NO to inhibit fast and slow stages of SSBs, DSBs, and HLS repair resulting in significant growth of genotoxic effect. DNA breaks generation from HLS is able to affect DSBs yields especially in cells with altered DNA repair. The process of DNA repair of delayed DSBs formed from HLS was quite different from removal of DNA damages occurring immediately after treatment and was characterized by IR dose dependent inhibition of DNA repair. Conclusion: High level of DNA strand breaks, that are generated after the combined treatment with NO and IR, are accumulated for quite a long time after exposure due to altered DNA repair, indicating the development of genetic instability and increase of carcinogenic risk for organism exposed to combination of harmful environmental factors.
issn 1812-9269
url https://nasplib.isofts.kiev.ua/handle/123456789/145268
citation_txt Exogenous nitric oxide potentiate DNA damage and alter DNA repair in cells exposed to ionising radiation / V.M. Mikhailenko, I.I. Muzalov // Experimental Oncology. — 2013. — Т. 35, № 4. — С. 318-324. — Бібліогр.: 43 назв. — англ.
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