Chitooligosaccharides antagonize the cytotoxic effect of glucosamine
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRN |
DOI: | 10.1007/s11274-011-0910-4 |
Texto Completo: | https://repositorio.ufrn.br/handle/123456789/32557 |
Resumo: | Chitooligosaccharides (COS) are partially hydrolyzed compounds derived from chitosan that exhibit a number of biological activities, including antitumor, antibacterial and antifungal properties. In this work, we examined the cytotoxicity of pure COS and oligomers A, B and C (solutions composed of different amounts of COS) produced by enzymatic hydrolysis using a crude enzyme extract produced by the fungus Metarhrizium anisopliae. The antiproliferative effect of these molecules was analyzed using tumor cell lines (HepG2 and HeLa cells) and in a normal cell line (3T3). The antioxidant activity was analyzed in several in vitro experiments. Glucosamine showed higher toxicity (approximately 92%) to all cell lines studied. However, the oligomers obtained after hydrolysis demonstrated no toxic effects on the normal cells (3T3). Furthermore, we showed that a small amount of other COS can decrease the cytotoxic effect of glucosamine against 3T3 cells, indicating that glucosamine could be used as an antitumor drug in the presence of other COS. In addition, different effects were found in antiproliferative assays, which depended on the COS composition in the oligomers (A, B and C), showing that a combination of them may be essential for developing antineoplastic drugs. Superoxide anion scavenging was the main antioxidant activity demonstrated by the COS and oligomers. This activity was also dependent on the oligomer composition of the chitosan hydrolysates. Further work will identify the ideal proportions of COS and glucosamine for maximizing the effects of these biological activities |
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Santos, Everaldo Silvino dosAssis, Cristiane Fernandes deCosta, Leandro SilvaMelo-Silveira, Raniere FagundesOliveira, Ruth MedeirosPagnoncelli, Maria Giovana BinderRocha, Hugo Alexandre OliveiraMacedo, Gorete Ribeiro de2021-05-25T13:18:23Z2021-05-25T13:18:23Z2012-10-02ASSIS, Cristiane Fernandes de; COSTA, Leandro Silva; MELO-SILVEIRA, Raniere Fagundes; OLIVEIRA, Ruth Medeiros; PAGNONCELLI, Maria Giovana Binder; ROCHA, Hugo Alexandre Oliveira; MACEDO, Gorete Ribeiro de; SANTOS, Everaldo Silvino dos. Chitooligosaccharides antagonize the cytotoxic effect of glucosamine. World Journal Of Microbiology And Biotechnology, [S.L.], v. 28, n. 3, p. 1097-1105, 2 out. 2011. Disponível em: https://link.springer.com/article/10.1007%2Fs11274-011-0910-4. Acesso em: 08 abr. 2021. http://dx.doi.org/10.1007/s11274-011-0910-4.0959-39931573-0972https://repositorio.ufrn.br/handle/123456789/3255710.1007/s11274-011-0910-4SpringerAttribution 3.0 Brazilhttp://creativecommons.org/licenses/by/3.0/br/info:eu-repo/semantics/openAccessGlucosamineChitosanMetarhrizium anisopliaeHeLaHepG23T3Chitooligosaccharides antagonize the cytotoxic effect of glucosamineinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleChitooligosaccharides (COS) are partially hydrolyzed compounds derived from chitosan that exhibit a number of biological activities, including antitumor, antibacterial and antifungal properties. In this work, we examined the cytotoxicity of pure COS and oligomers A, B and C (solutions composed of different amounts of COS) produced by enzymatic hydrolysis using a crude enzyme extract produced by the fungus Metarhrizium anisopliae. The antiproliferative effect of these molecules was analyzed using tumor cell lines (HepG2 and HeLa cells) and in a normal cell line (3T3). The antioxidant activity was analyzed in several in vitro experiments. Glucosamine showed higher toxicity (approximately 92%) to all cell lines studied. However, the oligomers obtained after hydrolysis demonstrated no toxic effects on the normal cells (3T3). Furthermore, we showed that a small amount of other COS can decrease the cytotoxic effect of glucosamine against 3T3 cells, indicating that glucosamine could be used as an antitumor drug in the presence of other COS. In addition, different effects were found in antiproliferative assays, which depended on the COS composition in the oligomers (A, B and C), showing that a combination of them may be essential for developing antineoplastic drugs. Superoxide anion scavenging was the main antioxidant activity demonstrated by the COS and oligomers. This activity was also dependent on the oligomer composition of the chitosan hydrolysates. Further work will identify the ideal proportions of COS and glucosamine for maximizing the effects of these biological activitiesengreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8914https://repositorio.ufrn.br/bitstream/123456789/32557/2/license_rdf4d2950bda3d176f570a9f8b328dfbbefMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/32557/3/license.txte9597aa2854d128fd968be5edc8a28d9MD53ORIGINALChitooligosaccharidesAntagonizeCytotoxic_Santos_2012.pdfChitooligosaccharidesAntagonizeCytotoxic_Santos_2012.pdfapplication/pdf431276https://repositorio.ufrn.br/bitstream/123456789/32557/1/ChitooligosaccharidesAntagonizeCytotoxic_Santos_2012.pdff65f7923e821ddd2dcc370d1e09daf44MD51123456789/325572021-05-25 10:18:25.172oai:https://repositorio.ufrn.br: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Repositório InstitucionalPUBhttp://repositorio.ufrn.br/oai/repositorio@bczm.ufrn.bropendoar:2021-05-25T13:18:25Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
dc.title.pt_BR.fl_str_mv |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
title |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
spellingShingle |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine Santos, Everaldo Silvino dos Glucosamine Chitosan Metarhrizium anisopliae HeLa HepG2 3T3 |
title_short |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
title_full |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
title_fullStr |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
title_full_unstemmed |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
title_sort |
Chitooligosaccharides antagonize the cytotoxic effect of glucosamine |
author |
Santos, Everaldo Silvino dos |
author_facet |
Santos, Everaldo Silvino dos Assis, Cristiane Fernandes de Costa, Leandro Silva Melo-Silveira, Raniere Fagundes Oliveira, Ruth Medeiros Pagnoncelli, Maria Giovana Binder Rocha, Hugo Alexandre Oliveira Macedo, Gorete Ribeiro de |
author_role |
author |
author2 |
Assis, Cristiane Fernandes de Costa, Leandro Silva Melo-Silveira, Raniere Fagundes Oliveira, Ruth Medeiros Pagnoncelli, Maria Giovana Binder Rocha, Hugo Alexandre Oliveira Macedo, Gorete Ribeiro de |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Santos, Everaldo Silvino dos Assis, Cristiane Fernandes de Costa, Leandro Silva Melo-Silveira, Raniere Fagundes Oliveira, Ruth Medeiros Pagnoncelli, Maria Giovana Binder Rocha, Hugo Alexandre Oliveira Macedo, Gorete Ribeiro de |
dc.subject.por.fl_str_mv |
Glucosamine Chitosan Metarhrizium anisopliae HeLa HepG2 3T3 |
topic |
Glucosamine Chitosan Metarhrizium anisopliae HeLa HepG2 3T3 |
description |
Chitooligosaccharides (COS) are partially hydrolyzed compounds derived from chitosan that exhibit a number of biological activities, including antitumor, antibacterial and antifungal properties. In this work, we examined the cytotoxicity of pure COS and oligomers A, B and C (solutions composed of different amounts of COS) produced by enzymatic hydrolysis using a crude enzyme extract produced by the fungus Metarhrizium anisopliae. The antiproliferative effect of these molecules was analyzed using tumor cell lines (HepG2 and HeLa cells) and in a normal cell line (3T3). The antioxidant activity was analyzed in several in vitro experiments. Glucosamine showed higher toxicity (approximately 92%) to all cell lines studied. However, the oligomers obtained after hydrolysis demonstrated no toxic effects on the normal cells (3T3). Furthermore, we showed that a small amount of other COS can decrease the cytotoxic effect of glucosamine against 3T3 cells, indicating that glucosamine could be used as an antitumor drug in the presence of other COS. In addition, different effects were found in antiproliferative assays, which depended on the COS composition in the oligomers (A, B and C), showing that a combination of them may be essential for developing antineoplastic drugs. Superoxide anion scavenging was the main antioxidant activity demonstrated by the COS and oligomers. This activity was also dependent on the oligomer composition of the chitosan hydrolysates. Further work will identify the ideal proportions of COS and glucosamine for maximizing the effects of these biological activities |
publishDate |
2012 |
dc.date.issued.fl_str_mv |
2012-10-02 |
dc.date.accessioned.fl_str_mv |
2021-05-25T13:18:23Z |
dc.date.available.fl_str_mv |
2021-05-25T13:18:23Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
ASSIS, Cristiane Fernandes de; COSTA, Leandro Silva; MELO-SILVEIRA, Raniere Fagundes; OLIVEIRA, Ruth Medeiros; PAGNONCELLI, Maria Giovana Binder; ROCHA, Hugo Alexandre Oliveira; MACEDO, Gorete Ribeiro de; SANTOS, Everaldo Silvino dos. Chitooligosaccharides antagonize the cytotoxic effect of glucosamine. World Journal Of Microbiology And Biotechnology, [S.L.], v. 28, n. 3, p. 1097-1105, 2 out. 2011. Disponível em: https://link.springer.com/article/10.1007%2Fs11274-011-0910-4. Acesso em: 08 abr. 2021. http://dx.doi.org/10.1007/s11274-011-0910-4. |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufrn.br/handle/123456789/32557 |
dc.identifier.issn.none.fl_str_mv |
0959-3993 1573-0972 |
dc.identifier.doi.none.fl_str_mv |
10.1007/s11274-011-0910-4 |
identifier_str_mv |
ASSIS, Cristiane Fernandes de; COSTA, Leandro Silva; MELO-SILVEIRA, Raniere Fagundes; OLIVEIRA, Ruth Medeiros; PAGNONCELLI, Maria Giovana Binder; ROCHA, Hugo Alexandre Oliveira; MACEDO, Gorete Ribeiro de; SANTOS, Everaldo Silvino dos. Chitooligosaccharides antagonize the cytotoxic effect of glucosamine. World Journal Of Microbiology And Biotechnology, [S.L.], v. 28, n. 3, p. 1097-1105, 2 out. 2011. Disponível em: https://link.springer.com/article/10.1007%2Fs11274-011-0910-4. Acesso em: 08 abr. 2021. http://dx.doi.org/10.1007/s11274-011-0910-4. 0959-3993 1573-0972 10.1007/s11274-011-0910-4 |
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https://repositorio.ufrn.br/handle/123456789/32557 |
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Attribution 3.0 Brazil http://creativecommons.org/licenses/by/3.0/br/ info:eu-repo/semantics/openAccess |
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Attribution 3.0 Brazil http://creativecommons.org/licenses/by/3.0/br/ |
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Springer |
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Springer |
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