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Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells

Resveratrol has received considerable attention as a polyphenol with anti-oxidant, anti-carcinogenic, and anti-inflammatory effects. Radiation is an important component of therapy for a wide range of malignant conditions. However, it causes damage to normal cells and, hence, can result in adverse si...

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Autores principales: Jeong, Min Ho, Yang, Kwang Mo, Jeong, Dong Hyeok, Lee, Chang Geun, Oh, Su Jung, Jeong, Soo Kyung, Lee, Ki Won, Jo, Young Rae, Jo, Wol Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014163/
https://www.ncbi.nlm.nih.gov/pubmed/24403520
http://dx.doi.org/10.1093/jrr/rrt140
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author Jeong, Min Ho
Yang, Kwang Mo
Jeong, Dong Hyeok
Lee, Chang Geun
Oh, Su Jung
Jeong, Soo Kyung
Lee, Ki Won
Jo, Young Rae
Jo, Wol Soon
author_facet Jeong, Min Ho
Yang, Kwang Mo
Jeong, Dong Hyeok
Lee, Chang Geun
Oh, Su Jung
Jeong, Soo Kyung
Lee, Ki Won
Jo, Young Rae
Jo, Wol Soon
author_sort Jeong, Min Ho
collection PubMed
description Resveratrol has received considerable attention as a polyphenol with anti-oxidant, anti-carcinogenic, and anti-inflammatory effects. Radiation is an important component of therapy for a wide range of malignant conditions. However, it causes damage to normal cells and, hence, can result in adverse side effects. This study was conducted to examine whether HS-1793, a novel resveratrol analogue free from the restriction of metabolic instability and the high dose requirement of resveratrol, induces a protective effect against radiation-induced DNA damage. HS-1793 effectively scavenged free radicals and inhibited radiation-induced plasmid DNA strand breaks in an in vitro assay. HS-1793 significantly decreased reactive oxygen species and cellular DNA damage in 2 Gy-irradiated Chinese hamster ovary (CHO)-K1 cells. In addition, HS-1793 dose-dependently reduced the levels of phosphorylated H2AX in irradiated CHO-K1 cells. These results indicate that HS-1793 has chemical radioprotective activity. Glutathione levels and superoxide dismutase activity in irradiated CHO-K1 cells increased significantly following HS-1793 treatment. The enhanced biological anti-oxidant activity and chemical radioprotective activity of HS-1793 maintained survival of irradiated CHO-K1 cells in a clonogenic assay. Therefore, HS-1793 may be of value as a radioprotector to protect healthy tissue surrounding tumor cells during radiotherapy to obtain better tumor control with a higher dose.
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spelling pubmed-40141632014-05-12 Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells Jeong, Min Ho Yang, Kwang Mo Jeong, Dong Hyeok Lee, Chang Geun Oh, Su Jung Jeong, Soo Kyung Lee, Ki Won Jo, Young Rae Jo, Wol Soon J Radiat Res Biology Resveratrol has received considerable attention as a polyphenol with anti-oxidant, anti-carcinogenic, and anti-inflammatory effects. Radiation is an important component of therapy for a wide range of malignant conditions. However, it causes damage to normal cells and, hence, can result in adverse side effects. This study was conducted to examine whether HS-1793, a novel resveratrol analogue free from the restriction of metabolic instability and the high dose requirement of resveratrol, induces a protective effect against radiation-induced DNA damage. HS-1793 effectively scavenged free radicals and inhibited radiation-induced plasmid DNA strand breaks in an in vitro assay. HS-1793 significantly decreased reactive oxygen species and cellular DNA damage in 2 Gy-irradiated Chinese hamster ovary (CHO)-K1 cells. In addition, HS-1793 dose-dependently reduced the levels of phosphorylated H2AX in irradiated CHO-K1 cells. These results indicate that HS-1793 has chemical radioprotective activity. Glutathione levels and superoxide dismutase activity in irradiated CHO-K1 cells increased significantly following HS-1793 treatment. The enhanced biological anti-oxidant activity and chemical radioprotective activity of HS-1793 maintained survival of irradiated CHO-K1 cells in a clonogenic assay. Therefore, HS-1793 may be of value as a radioprotector to protect healthy tissue surrounding tumor cells during radiotherapy to obtain better tumor control with a higher dose. Oxford University Press 2014-05 2014-01-07 /pmc/articles/PMC4014163/ /pubmed/24403520 http://dx.doi.org/10.1093/jrr/rrt140 Text en © The Author 2014. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biology
Jeong, Min Ho
Yang, Kwang Mo
Jeong, Dong Hyeok
Lee, Chang Geun
Oh, Su Jung
Jeong, Soo Kyung
Lee, Ki Won
Jo, Young Rae
Jo, Wol Soon
Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells
title Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells
title_full Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells
title_fullStr Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells
title_full_unstemmed Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells
title_short Protective activity of a novel resveratrol analogue, HS-1793, against DNA damage in (137)Cs-irradiated CHO-K1 cells
title_sort protective activity of a novel resveratrol analogue, hs-1793, against dna damage in (137)cs-irradiated cho-k1 cells
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014163/
https://www.ncbi.nlm.nih.gov/pubmed/24403520
http://dx.doi.org/10.1093/jrr/rrt140
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