Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/146832 |
Resumo: | The purpose of our study was to divulge the antiproliferative effect of an ethanolic extract of Algerian propolis (EEP) in the human lung adenocarcinoma cell line (A549) and reveal the chemopreventive role against benzo(a)pyrene-induced lung carcinogenesis in albino Wistar rats. Cytotoxicity of EEP was evaluated using the MTT assay and cell adhesion in A549 cells. Moreover, rats were given 25 mg/kg of propolis for 5 days before induction of experimental lung cancer by a single intraperitoneal dose of 200 mg/kg benzo(a)pyrene. Body weight, lung weight, lipid peroxidation, marker enzymes, and enzymatic and non-enzymatic antioxidants were estimated. The EEP demonstrated an inhibitory effect on proliferation of A549 at 24 and 72 hours in a dose-dependent manner and blocked adhesion of the cells by fibrinogen. Moreover, EEP reduced the oxidative stress generated by benzo(a)pyrene. The pre-treatment showed that enzymatic and non-enzymatic antioxidants increased and lipid peroxidation decreased. A histological analysis further supported these findings and showed a decrease in the number of side effects. These results are particularly important for both clinical applications of propolis and the possibility for its use as a potential chemotherapeutic agent. |
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Brazilian Journal of Pharmaceutical Sciences |
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Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activityAlgerian propolis/effectsBenzo(a)pyreneChemopreventionLung cancerOxidative stress. The purpose of our study was to divulge the antiproliferative effect of an ethanolic extract of Algerian propolis (EEP) in the human lung adenocarcinoma cell line (A549) and reveal the chemopreventive role against benzo(a)pyrene-induced lung carcinogenesis in albino Wistar rats. Cytotoxicity of EEP was evaluated using the MTT assay and cell adhesion in A549 cells. Moreover, rats were given 25 mg/kg of propolis for 5 days before induction of experimental lung cancer by a single intraperitoneal dose of 200 mg/kg benzo(a)pyrene. Body weight, lung weight, lipid peroxidation, marker enzymes, and enzymatic and non-enzymatic antioxidants were estimated. The EEP demonstrated an inhibitory effect on proliferation of A549 at 24 and 72 hours in a dose-dependent manner and blocked adhesion of the cells by fibrinogen. Moreover, EEP reduced the oxidative stress generated by benzo(a)pyrene. The pre-treatment showed that enzymatic and non-enzymatic antioxidants increased and lipid peroxidation decreased. A histological analysis further supported these findings and showed a decrease in the number of side effects. These results are particularly important for both clinical applications of propolis and the possibility for its use as a potential chemotherapeutic agent.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2018-06-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/14683210.1590/s2175-97902018000117396Brazilian Journal of Pharmaceutical Sciences; Vol. 54 Núm. 1 (2018); e17396Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 1 (2018); e17396Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 1 (2018); e173962175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/146832/140361Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessBrihoum, HadjerMaiza, MhamedSahali, HafidaBoulmeltout, MalikaBarratt, GillianBenguedouar, LamiaLahouel, Mesbah2018-06-07T16:31:56Zoai:revistas.usp.br:article/146832Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2018-06-07T16:31:56Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
title |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
spellingShingle |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity Brihoum, Hadjer Algerian propolis/effects Benzo(a)pyrene Chemoprevention Lung cancer Oxidative stress. |
title_short |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
title_full |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
title_fullStr |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
title_full_unstemmed |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
title_sort |
Dual effect of Algerian propolis on lung cancer: antitumor and chemopreventive effects involving antioxidant activity |
author |
Brihoum, Hadjer |
author_facet |
Brihoum, Hadjer Maiza, Mhamed Sahali, Hafida Boulmeltout, Malika Barratt, Gillian Benguedouar, Lamia Lahouel, Mesbah |
author_role |
author |
author2 |
Maiza, Mhamed Sahali, Hafida Boulmeltout, Malika Barratt, Gillian Benguedouar, Lamia Lahouel, Mesbah |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Brihoum, Hadjer Maiza, Mhamed Sahali, Hafida Boulmeltout, Malika Barratt, Gillian Benguedouar, Lamia Lahouel, Mesbah |
dc.subject.por.fl_str_mv |
Algerian propolis/effects Benzo(a)pyrene Chemoprevention Lung cancer Oxidative stress. |
topic |
Algerian propolis/effects Benzo(a)pyrene Chemoprevention Lung cancer Oxidative stress. |
description |
The purpose of our study was to divulge the antiproliferative effect of an ethanolic extract of Algerian propolis (EEP) in the human lung adenocarcinoma cell line (A549) and reveal the chemopreventive role against benzo(a)pyrene-induced lung carcinogenesis in albino Wistar rats. Cytotoxicity of EEP was evaluated using the MTT assay and cell adhesion in A549 cells. Moreover, rats were given 25 mg/kg of propolis for 5 days before induction of experimental lung cancer by a single intraperitoneal dose of 200 mg/kg benzo(a)pyrene. Body weight, lung weight, lipid peroxidation, marker enzymes, and enzymatic and non-enzymatic antioxidants were estimated. The EEP demonstrated an inhibitory effect on proliferation of A549 at 24 and 72 hours in a dose-dependent manner and blocked adhesion of the cells by fibrinogen. Moreover, EEP reduced the oxidative stress generated by benzo(a)pyrene. The pre-treatment showed that enzymatic and non-enzymatic antioxidants increased and lipid peroxidation decreased. A histological analysis further supported these findings and showed a decrease in the number of side effects. These results are particularly important for both clinical applications of propolis and the possibility for its use as a potential chemotherapeutic agent. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-06-07 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/146832 10.1590/s2175-97902018000117396 |
url |
https://www.revistas.usp.br/bjps/article/view/146832 |
identifier_str_mv |
10.1590/s2175-97902018000117396 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/146832/140361 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso) |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 54 Núm. 1 (2018); e17396 Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 1 (2018); e17396 Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 1 (2018); e17396 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Brazilian Journal of Pharmaceutical Sciences |
collection |
Brazilian Journal of Pharmaceutical Sciences |
repository.name.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
bjps@usp.br||elizabeth.igne@gmail.com |
_version_ |
1800222913375240192 |