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Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage

Neolignans are secondary metabolites found in various groups of Angiosperms. They belong to a class of natural compounds with great diversity of chemical structures and pharmacological activities. These compounds are formed by linking two phenylpropanoid units. Several compounds that have ability to...

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Autores principales: Hanusch, Alex Lucas, de Oliveira, Guilherme Roberto, de Sabóia-Morais, Simone Maria Teixeira, Machado, Rafael Cosme, dos Anjos, Murilo Machado, Chen Chen, Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640812/
https://www.ncbi.nlm.nih.gov/pubmed/26554835
http://dx.doi.org/10.1371/journal.pone.0142284
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author Hanusch, Alex Lucas
de Oliveira, Guilherme Roberto
de Sabóia-Morais, Simone Maria Teixeira
Machado, Rafael Cosme
dos Anjos, Murilo Machado
Chen Chen, Lee
author_facet Hanusch, Alex Lucas
de Oliveira, Guilherme Roberto
de Sabóia-Morais, Simone Maria Teixeira
Machado, Rafael Cosme
dos Anjos, Murilo Machado
Chen Chen, Lee
author_sort Hanusch, Alex Lucas
collection PubMed
description Neolignans are secondary metabolites found in various groups of Angiosperms. They belong to a class of natural compounds with great diversity of chemical structures and pharmacological activities. These compounds are formed by linking two phenylpropanoid units. Several compounds that have ability to prevent genetic damage have been isolated from plants, and can be used to prevent or delay the development of tumor cells. Genetic toxicology evaluation is widely used in risk assessment of new drugs in preclinical screening tests. In this study, we evaluated the genotoxicity and cytotoxicity of the neolignan analogue 2-(4-nitrophenoxy)-1-phenylethanone (4NF) and its protective effect against DNA damage using the mouse bone marrow micronucleus test and the comet assay in mouse peripheral blood. Our results showed that this neolignan analogue had no genotoxic activity and was able to reduce induced damage both in mouse bone marrow and peripheral blood. Although the neolignan analogue 4NF was cytotoxic, it reduced cyclophosphamide-induced cytotoxicity. In conclusion, it showed no genotoxic action, but exhibited cytotoxic, antigenotoxic, and anticytotoxic activities.
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spelling pubmed-46408122015-11-13 Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage Hanusch, Alex Lucas de Oliveira, Guilherme Roberto de Sabóia-Morais, Simone Maria Teixeira Machado, Rafael Cosme dos Anjos, Murilo Machado Chen Chen, Lee PLoS One Research Article Neolignans are secondary metabolites found in various groups of Angiosperms. They belong to a class of natural compounds with great diversity of chemical structures and pharmacological activities. These compounds are formed by linking two phenylpropanoid units. Several compounds that have ability to prevent genetic damage have been isolated from plants, and can be used to prevent or delay the development of tumor cells. Genetic toxicology evaluation is widely used in risk assessment of new drugs in preclinical screening tests. In this study, we evaluated the genotoxicity and cytotoxicity of the neolignan analogue 2-(4-nitrophenoxy)-1-phenylethanone (4NF) and its protective effect against DNA damage using the mouse bone marrow micronucleus test and the comet assay in mouse peripheral blood. Our results showed that this neolignan analogue had no genotoxic activity and was able to reduce induced damage both in mouse bone marrow and peripheral blood. Although the neolignan analogue 4NF was cytotoxic, it reduced cyclophosphamide-induced cytotoxicity. In conclusion, it showed no genotoxic action, but exhibited cytotoxic, antigenotoxic, and anticytotoxic activities. Public Library of Science 2015-11-10 /pmc/articles/PMC4640812/ /pubmed/26554835 http://dx.doi.org/10.1371/journal.pone.0142284 Text en © 2015 Hanusch 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
Hanusch, Alex Lucas
de Oliveira, Guilherme Roberto
de Sabóia-Morais, Simone Maria Teixeira
Machado, Rafael Cosme
dos Anjos, Murilo Machado
Chen Chen, Lee
Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage
title Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage
title_full Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage
title_fullStr Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage
title_full_unstemmed Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage
title_short Genotoxicity and Cytotoxicity Evaluation of the Neolignan Analogue 2-(4-Nitrophenoxy)-1Phenylethanone and its Protective Effect Against DNA Damage
title_sort genotoxicity and cytotoxicity evaluation of the neolignan analogue 2-(4-nitrophenoxy)-1phenylethanone and its protective effect against dna damage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640812/
https://www.ncbi.nlm.nih.gov/pubmed/26554835
http://dx.doi.org/10.1371/journal.pone.0142284
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