Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model

The aim of this study was to assess the effect of oral administration of Hydroalcoholic Extract of Green Propolis (HEGP) on dermal carcinogenesis in rodent model. For the biological assay, we used 36 mice, assigned into 6 groups (n=6): CTR (treated with 100 mg/kg HEGP and no tumor induction), TUM (treated with water and tumor induction), GP10 (treated with 10 mg/kg HEGP and tumor induction), GP50 (treated with 50 mg/kg HEGP and tumor induction) and GP100 (treated with 100 mg/kg HEGP and tumor induction). Cancer induction was performed in the back of the mice by topical application of DMBA. After 16 weeks, mice were euthanized and their backs were submitted to post-mortem histological analysis. The mean number of lesions developed in TUM (4.14±0.89) was significantly higher than in GP10 (2.05±1.02), GP50 (1.8±1.92) and GP100 (2.5±1.73) (p<0.05). The tumors formed in HEGP-treated groups were histologically more differentiated, but only in PV100 in situ lesions were evidenced. Infiltration of anatomical noble structures was less frequent in HEGP-treated groups (p<0.05). Our data suggest that oral administration of HEGP provided partial inhibition of DMBA-induced dermal carcinogenesis, as well as appeared to modulate the differentiation and infiltrative potential of the carcinomas in rodent model.

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Main Authors: Pereira-Filho,Rose Nely, Batista,Fellipe Santos, Ribeiro,Danielle Rodrigues, Melo,Genecy Calado de, Reis,Francisco Prado, Melo,Allan Ulisses Carvalho de, Gomes,Margarete Zanardo, Cardoso,Juliana Cordeiro, Albuquerque Júnior,Ricardo Luiz Cavalcanti de
Format: Digital revista
Language:English
Published: Sociedad Chilena de Anatomía 2014
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022014000200024
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spelling oai:scielo:S0717-950220140002000242015-11-16Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine ModelPereira-Filho,Rose NelyBatista,Fellipe SantosRibeiro,Danielle RodriguesMelo,Genecy Calado deReis,Francisco PradoMelo,Allan Ulisses Carvalho deGomes,Margarete ZanardoCardoso,Juliana CordeiroAlbuquerque Júnior,Ricardo Luiz Cavalcanti de Propolis Skin cancer The aim of this study was to assess the effect of oral administration of Hydroalcoholic Extract of Green Propolis (HEGP) on dermal carcinogenesis in rodent model. For the biological assay, we used 36 mice, assigned into 6 groups (n=6): CTR (treated with 100 mg/kg HEGP and no tumor induction), TUM (treated with water and tumor induction), GP10 (treated with 10 mg/kg HEGP and tumor induction), GP50 (treated with 50 mg/kg HEGP and tumor induction) and GP100 (treated with 100 mg/kg HEGP and tumor induction). Cancer induction was performed in the back of the mice by topical application of DMBA. After 16 weeks, mice were euthanized and their backs were submitted to post-mortem histological analysis. The mean number of lesions developed in TUM (4.14±0.89) was significantly higher than in GP10 (2.05±1.02), GP50 (1.8±1.92) and GP100 (2.5±1.73) (p<0.05). The tumors formed in HEGP-treated groups were histologically more differentiated, but only in PV100 in situ lesions were evidenced. Infiltration of anatomical noble structures was less frequent in HEGP-treated groups (p<0.05). Our data suggest that oral administration of HEGP provided partial inhibition of DMBA-induced dermal carcinogenesis, as well as appeared to modulate the differentiation and infiltrative potential of the carcinomas in rodent model.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.32 n.2 20142014-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022014000200024en10.4067/S0717-95022014000200024
institution SCIELO
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country Chile
countrycode CL
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region America del Sur
libraryname SciELO
language English
format Digital
author Pereira-Filho,Rose Nely
Batista,Fellipe Santos
Ribeiro,Danielle Rodrigues
Melo,Genecy Calado de
Reis,Francisco Prado
Melo,Allan Ulisses Carvalho de
Gomes,Margarete Zanardo
Cardoso,Juliana Cordeiro
Albuquerque Júnior,Ricardo Luiz Cavalcanti de
spellingShingle Pereira-Filho,Rose Nely
Batista,Fellipe Santos
Ribeiro,Danielle Rodrigues
Melo,Genecy Calado de
Reis,Francisco Prado
Melo,Allan Ulisses Carvalho de
Gomes,Margarete Zanardo
Cardoso,Juliana Cordeiro
Albuquerque Júnior,Ricardo Luiz Cavalcanti de
Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model
author_facet Pereira-Filho,Rose Nely
Batista,Fellipe Santos
Ribeiro,Danielle Rodrigues
Melo,Genecy Calado de
Reis,Francisco Prado
Melo,Allan Ulisses Carvalho de
Gomes,Margarete Zanardo
Cardoso,Juliana Cordeiro
Albuquerque Júnior,Ricardo Luiz Cavalcanti de
author_sort Pereira-Filho,Rose Nely
title Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model
title_short Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model
title_full Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model
title_fullStr Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model
title_full_unstemmed Chemopreventive Effect of Brazilian Green Propolis on Experimental Dermal Carcinogenesis in Murine Model
title_sort chemopreventive effect of brazilian green propolis on experimental dermal carcinogenesis in murine model
description The aim of this study was to assess the effect of oral administration of Hydroalcoholic Extract of Green Propolis (HEGP) on dermal carcinogenesis in rodent model. For the biological assay, we used 36 mice, assigned into 6 groups (n=6): CTR (treated with 100 mg/kg HEGP and no tumor induction), TUM (treated with water and tumor induction), GP10 (treated with 10 mg/kg HEGP and tumor induction), GP50 (treated with 50 mg/kg HEGP and tumor induction) and GP100 (treated with 100 mg/kg HEGP and tumor induction). Cancer induction was performed in the back of the mice by topical application of DMBA. After 16 weeks, mice were euthanized and their backs were submitted to post-mortem histological analysis. The mean number of lesions developed in TUM (4.14±0.89) was significantly higher than in GP10 (2.05±1.02), GP50 (1.8±1.92) and GP100 (2.5±1.73) (p<0.05). The tumors formed in HEGP-treated groups were histologically more differentiated, but only in PV100 in situ lesions were evidenced. Infiltration of anatomical noble structures was less frequent in HEGP-treated groups (p<0.05). Our data suggest that oral administration of HEGP provided partial inhibition of DMBA-induced dermal carcinogenesis, as well as appeared to modulate the differentiation and infiltrative potential of the carcinomas in rodent model.
publisher Sociedad Chilena de Anatomía
publishDate 2014
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022014000200024
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