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Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen
BACKGROUND: Ginkgo biloba extract (GbE) is used extensively by breast cancer patients undergoing treatment with Tamoxifen (TAM). Thus, the present study investigated the effects of GbE in female Sprague–Dawley (SD) rats bearing chemically-induced mammary tumors and receiving TAM. METHODS: Animals be...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655872/ https://www.ncbi.nlm.nih.gov/pubmed/23634930 http://dx.doi.org/10.1186/1472-6882-13-93 |
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author | Dias, Marcos Correa Furtado, Kelly Silva Rodrigues, Maria Aparecida Marchesan Barbisan, Luís Fernando |
author_facet | Dias, Marcos Correa Furtado, Kelly Silva Rodrigues, Maria Aparecida Marchesan Barbisan, Luís Fernando |
author_sort | Dias, Marcos Correa |
collection | PubMed |
description | BACKGROUND: Ginkgo biloba extract (GbE) is used extensively by breast cancer patients undergoing treatment with Tamoxifen (TAM). Thus, the present study investigated the effects of GbE in female Sprague–Dawley (SD) rats bearing chemically-induced mammary tumors and receiving TAM. METHODS: Animals bearing mammary tumors (≥1 cm in diameter) were divided into four groups: TAM [10 mg/kg, intragastrically (i.g.)], TAM plus GbE [50 and 100 mg/kg, intraperitoneally (i.p.)] or an untreated control group. After 4 weeks, the therapeutic efficacy of the different treatments was evaluated by measuring the tumor volume (cm(3)) and the proportions of each tumor that were alive, necrotic or degenerative (mm(2)). In addition, labeling indexes (LI%) were calculated for cell proliferation (PCNA LI%) and apoptosis (cleaved caspase-3 LI%), expression of estrogen receptor-alpha (ER-α) and p63 biomarkers. RESULTS: Overall, the tumor volume and the PCNA LI% within live tumor areas were reduced by 83% and 99%, respectively, in all TAM-treated groups when compared to the untreated control group. GbE treatment (100 mg/kg) reduced the proportions of live (24.8%) and necrotic areas (2.9%) (p = 0.046 and p = 0.038, respectively) and significantly increased the proportion of degenerative areas (72.9%) (p = 0.004) in mammary tumors when compared to the group treated only with TAM. The expression of ER-α, p63 and cleaved caspase-3 in live tumor tissues was not modified by GbE treatment. CONCLUSIONS: Co-treatment with 100 mg/kg GbE presented a slightly beneficial effect on the therapeutic efficacy of TAM in female SD rats bearing mammary tumors. |
format | Online Article Text |
id | pubmed-3655872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36558722013-05-17 Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen Dias, Marcos Correa Furtado, Kelly Silva Rodrigues, Maria Aparecida Marchesan Barbisan, Luís Fernando BMC Complement Altern Med Research Article BACKGROUND: Ginkgo biloba extract (GbE) is used extensively by breast cancer patients undergoing treatment with Tamoxifen (TAM). Thus, the present study investigated the effects of GbE in female Sprague–Dawley (SD) rats bearing chemically-induced mammary tumors and receiving TAM. METHODS: Animals bearing mammary tumors (≥1 cm in diameter) were divided into four groups: TAM [10 mg/kg, intragastrically (i.g.)], TAM plus GbE [50 and 100 mg/kg, intraperitoneally (i.p.)] or an untreated control group. After 4 weeks, the therapeutic efficacy of the different treatments was evaluated by measuring the tumor volume (cm(3)) and the proportions of each tumor that were alive, necrotic or degenerative (mm(2)). In addition, labeling indexes (LI%) were calculated for cell proliferation (PCNA LI%) and apoptosis (cleaved caspase-3 LI%), expression of estrogen receptor-alpha (ER-α) and p63 biomarkers. RESULTS: Overall, the tumor volume and the PCNA LI% within live tumor areas were reduced by 83% and 99%, respectively, in all TAM-treated groups when compared to the untreated control group. GbE treatment (100 mg/kg) reduced the proportions of live (24.8%) and necrotic areas (2.9%) (p = 0.046 and p = 0.038, respectively) and significantly increased the proportion of degenerative areas (72.9%) (p = 0.004) in mammary tumors when compared to the group treated only with TAM. The expression of ER-α, p63 and cleaved caspase-3 in live tumor tissues was not modified by GbE treatment. CONCLUSIONS: Co-treatment with 100 mg/kg GbE presented a slightly beneficial effect on the therapeutic efficacy of TAM in female SD rats bearing mammary tumors. BioMed Central 2013-05-01 /pmc/articles/PMC3655872/ /pubmed/23634930 http://dx.doi.org/10.1186/1472-6882-13-93 Text en Copyright © 2013 Dias et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Dias, Marcos Correa Furtado, Kelly Silva Rodrigues, Maria Aparecida Marchesan Barbisan, Luís Fernando Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
title | Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
title_full | Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
title_fullStr | Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
title_full_unstemmed | Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
title_short | Effects of Ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
title_sort | effects of ginkgo biloba on chemically-induced mammary tumors in rats receiving tamoxifen |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655872/ https://www.ncbi.nlm.nih.gov/pubmed/23634930 http://dx.doi.org/10.1186/1472-6882-13-93 |
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