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Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals

As a well known anti-neoplastic drug, the cytogenotoxicity of methotrexate (MTX) has received more attention in recent years. To develop a new cytoprotector to reduce the risk of second cancers caused by methotrexate, an umu test combined with a micronucleus assay was employed to estimate the cytopr...

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Autores principales: Gu, Shaobin, Wu, Ying, Yang, Jianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867711/
https://www.ncbi.nlm.nih.gov/pubmed/27190706
http://dx.doi.org/10.7717/peerj.1983
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author Gu, Shaobin
Wu, Ying
Yang, Jianbo
author_facet Gu, Shaobin
Wu, Ying
Yang, Jianbo
author_sort Gu, Shaobin
collection PubMed
description As a well known anti-neoplastic drug, the cytogenotoxicity of methotrexate (MTX) has received more attention in recent years. To develop a new cytoprotector to reduce the risk of second cancers caused by methotrexate, an umu test combined with a micronucleus assay was employed to estimate the cytoprotective effects of ten kinds of bioactive phytochemicals and their combinations. The results showed that allicin, proanthocyanidins, polyphenols, eleutherosides and isoflavones had higher antimutagenic activities than other phytochemicals. At the highest dose tested, the MTX genetoxicity was suppressed by 34.03%∼67.12%. Of all the bioactive phytochemical combinations, the combination of grape seed proanthocyanidins and eleutherosides from Siberian ginseng as well as green tea polyphenols and eleutherosides exhibited stronger antimutagenic effects; the inhibition rate of methotrexate-induced genotoxicity separately reached 74.7 ± 6.5% and 71.8 ± 4.7%. Pretreatment of Kunming mice with phytochemical combinations revealed an obvious reduction in micronucleus and sperm abnormality rates following exposure to MTX (p < 0.01). Moreover, significant increases in thymus and spleen indices were observed in cytoprotector candidates in treated groups. The results indicated that bioactive phytochemicals combinations had the potential to be used as new cytoprotectors.
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spelling pubmed-48677112016-05-17 Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals Gu, Shaobin Wu, Ying Yang, Jianbo PeerJ Biochemistry As a well known anti-neoplastic drug, the cytogenotoxicity of methotrexate (MTX) has received more attention in recent years. To develop a new cytoprotector to reduce the risk of second cancers caused by methotrexate, an umu test combined with a micronucleus assay was employed to estimate the cytoprotective effects of ten kinds of bioactive phytochemicals and their combinations. The results showed that allicin, proanthocyanidins, polyphenols, eleutherosides and isoflavones had higher antimutagenic activities than other phytochemicals. At the highest dose tested, the MTX genetoxicity was suppressed by 34.03%∼67.12%. Of all the bioactive phytochemical combinations, the combination of grape seed proanthocyanidins and eleutherosides from Siberian ginseng as well as green tea polyphenols and eleutherosides exhibited stronger antimutagenic effects; the inhibition rate of methotrexate-induced genotoxicity separately reached 74.7 ± 6.5% and 71.8 ± 4.7%. Pretreatment of Kunming mice with phytochemical combinations revealed an obvious reduction in micronucleus and sperm abnormality rates following exposure to MTX (p < 0.01). Moreover, significant increases in thymus and spleen indices were observed in cytoprotector candidates in treated groups. The results indicated that bioactive phytochemicals combinations had the potential to be used as new cytoprotectors. PeerJ Inc. 2016-05-11 /pmc/articles/PMC4867711/ /pubmed/27190706 http://dx.doi.org/10.7717/peerj.1983 Text en ©2016 Gu 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Gu, Shaobin
Wu, Ying
Yang, Jianbo
Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
title Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
title_full Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
title_fullStr Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
title_full_unstemmed Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
title_short Screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
title_sort screening of cytoprotectors against methotrexate-induced cytogenotoxicity from bioactive phytochemicals
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867711/
https://www.ncbi.nlm.nih.gov/pubmed/27190706
http://dx.doi.org/10.7717/peerj.1983
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