In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English]
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | por eng |
Título da fonte: | Scientia Medica (Porto Alegre. Online) |
Texto Completo: | https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790 |
Resumo: | AIMS: To determine cell viability compared to the biological effect of Salvia officinalis L. extract on cultured tumor cells of the larynx (Hep-2) and in human hepatoma cells (HepG2) METHODS: Tumor cells Hep-2 and HepG2 were grown in DMEM (Dulbecco's Modified Eagle Medium) supplemented with 10% inactivated fetal bovine serum and 1% antibiotics (Penicillin/Streptomycin), in incubator at 37°C and humidified with 5% CO2. In the second step they were plated (5 x 104 cells/mL) in 96 well plates during 24 hours to obtain 60-70% confluency, and treated with the hydroalcoholic extract of Salvia officinalis L., negative control with 80% ethanol (v/v) and positive control of hydrogen peroxide (H2O2), t-butyl peroxide hidroxy (TBO), doxorubicin and cisplatin. Cell viability was determined by MTT reduction (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). Results were analyzed by Tukey test (p≤0,05) using the SPSS v.19. RESULTS: the hydroalcoholic extract of Salvia officinalis L. showed cytotoxic activity to tumor cells Hep-2 IC50 0,38 ± 0.02 mg/mL for HepG2 IC50 0,54 ± 0.03 mg/mL compared to negative control, staying above the IC50 obtained for their positive controls. Cisplatin showed IC50 below the extract of sage, but to obtain their IC50 was increased exposure time in six hours. CONCLUSIONS: the results of this study suggest that the extract of Salvia officinalis L. has biological activity against tumor cell; further studies are needed to confirm its efficacy and its potential role in cancer treatment. |
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In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English]Avaliação in vitro do potencial biológico da Salvia officinalis L. em células tumoraisSALVIA OFFICINALISCELL SURVIVALANTINEOPLASTIC AGENTSTHERAPY.Salvia officinalisSOBREVIVÊNCIA CELULARANTINEOPLÁSICOSTERAPÊUTICA.AIMS: To determine cell viability compared to the biological effect of Salvia officinalis L. extract on cultured tumor cells of the larynx (Hep-2) and in human hepatoma cells (HepG2) METHODS: Tumor cells Hep-2 and HepG2 were grown in DMEM (Dulbecco's Modified Eagle Medium) supplemented with 10% inactivated fetal bovine serum and 1% antibiotics (Penicillin/Streptomycin), in incubator at 37°C and humidified with 5% CO2. In the second step they were plated (5 x 104 cells/mL) in 96 well plates during 24 hours to obtain 60-70% confluency, and treated with the hydroalcoholic extract of Salvia officinalis L., negative control with 80% ethanol (v/v) and positive control of hydrogen peroxide (H2O2), t-butyl peroxide hidroxy (TBO), doxorubicin and cisplatin. Cell viability was determined by MTT reduction (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). Results were analyzed by Tukey test (p≤0,05) using the SPSS v.19. RESULTS: the hydroalcoholic extract of Salvia officinalis L. showed cytotoxic activity to tumor cells Hep-2 IC50 0,38 ± 0.02 mg/mL for HepG2 IC50 0,54 ± 0.03 mg/mL compared to negative control, staying above the IC50 obtained for their positive controls. Cisplatin showed IC50 below the extract of sage, but to obtain their IC50 was increased exposure time in six hours. CONCLUSIONS: the results of this study suggest that the extract of Salvia officinalis L. has biological activity against tumor cell; further studies are needed to confirm its efficacy and its potential role in cancer treatment.OBJETIVOS: Determinar a viabilidade celular frente ao efeito biológico do extrato hidroalcoólico de Salvia officinalis L. em culturas de células tumorais de laringe (Hep-2) e células de hepatoma humano (HepG2). MÉTODOS: Células tumorais Hep-2 e HepG2 foram cultivadas em meio DMEM (Dulbecco’s Modified Eagle Médium) suplementado com 10% soro fetal bovino inativado e 1% de antibiótico (Penicilina/Estreptomicina) em estufa a 37°C e atmosfera umidificada com 5% de CO2. Na segunda etapa foram semeadas (5 x 104 células/mL) em placas de 96 poços durante o período de 24 horas até obtenção de 60-70% de confluência e realizou-se o tratamento das células com extrato hidroalcoólico de Salvia officinalis L., controle negativo de etanol 80% (v/v) e controles positivos de peróxido de hidrogênio (H2O2), t-butil hidroxi peroxido (TBO), doxorrubicina e cisplatina. A viabilidade celular foi determinada pela redução do MTT (brometo de 3- (4,5 dimetiltiazol-2-il)-2,5-difeniltetrazolio). Os resultados foram analisados pelo teste de Tukey no programa SPSS v.19. RESULTADOS: O extrato hidroalcoólico de Salvia officinalis L. mostrou atividade citotóxica para células tumorais Hep-2 IC50 0,38±0,02 mg/mL e para HepG2 IC50 0,54±0,03 mg/mL em comparação ao controle negativo, ficando acima do IC50 obtido para seus controles positivos. A cisplatina apresentou IC50 abaixo do extrato de sálvia, porém para a obtenção do seu IC50 aumentou-se o tempo de exposição em seis horas. CONCLUSÕES: sugere-se que o extrato de Salvia officinalis L. tem atividade biológica em células tumorais, podendo ser objetivo de mais estudos com a finalidade de comprovar sua eficácia como possível agente para o tratamento do câncer.Editora da PUCRS - ediPUCRS2012-07-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790Scientia Medica; Vol. 22 No. 3 (2012); 131-137Scientia Medica; v. 22 n. 3 (2012); 131-1371980-61081806-5562reponame:Scientia Medica (Porto Alegre. Online)instname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)instacron:PUC_RSporenghttps://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790/8178https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790/8179https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790/8180Garcia, Charlene Silvestrin CeliLambert, Ana Paula FrancoHenriques, João Antonio PêgasEly, Mariana Roeschinfo:eu-repo/semantics/openAccess2013-07-15T18:40:59Zoai:ojs.revistaseletronicas.pucrs.br:article/10790Revistahttps://revistaseletronicas.pucrs.br/scientiamedica/PUBhttps://revistaseletronicas.pucrs.br/scientiamedica/oaiscientiamedica@pucrs.br || editora.periodicos@pucrs.br1980-61081806-5562opendoar:2013-07-15T18:40:59Scientia Medica (Porto Alegre. Online) - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS)false |
dc.title.none.fl_str_mv |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] Avaliação in vitro do potencial biológico da Salvia officinalis L. em células tumorais |
title |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] |
spellingShingle |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] Garcia, Charlene Silvestrin Celi SALVIA OFFICINALIS CELL SURVIVAL ANTINEOPLASTIC AGENTS THERAPY. Salvia officinalis SOBREVIVÊNCIA CELULAR ANTINEOPLÁSICOS TERAPÊUTICA. |
title_short |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] |
title_full |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] |
title_fullStr |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] |
title_full_unstemmed |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] |
title_sort |
In vitro evaluation of the biological potential of Salvia officinalis L. in tumor cells [Abstract in English] |
author |
Garcia, Charlene Silvestrin Celi |
author_facet |
Garcia, Charlene Silvestrin Celi Lambert, Ana Paula Franco Henriques, João Antonio Pêgas Ely, Mariana Roesch |
author_role |
author |
author2 |
Lambert, Ana Paula Franco Henriques, João Antonio Pêgas Ely, Mariana Roesch |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Garcia, Charlene Silvestrin Celi Lambert, Ana Paula Franco Henriques, João Antonio Pêgas Ely, Mariana Roesch |
dc.subject.por.fl_str_mv |
SALVIA OFFICINALIS CELL SURVIVAL ANTINEOPLASTIC AGENTS THERAPY. Salvia officinalis SOBREVIVÊNCIA CELULAR ANTINEOPLÁSICOS TERAPÊUTICA. |
topic |
SALVIA OFFICINALIS CELL SURVIVAL ANTINEOPLASTIC AGENTS THERAPY. Salvia officinalis SOBREVIVÊNCIA CELULAR ANTINEOPLÁSICOS TERAPÊUTICA. |
description |
AIMS: To determine cell viability compared to the biological effect of Salvia officinalis L. extract on cultured tumor cells of the larynx (Hep-2) and in human hepatoma cells (HepG2) METHODS: Tumor cells Hep-2 and HepG2 were grown in DMEM (Dulbecco's Modified Eagle Medium) supplemented with 10% inactivated fetal bovine serum and 1% antibiotics (Penicillin/Streptomycin), in incubator at 37°C and humidified with 5% CO2. In the second step they were plated (5 x 104 cells/mL) in 96 well plates during 24 hours to obtain 60-70% confluency, and treated with the hydroalcoholic extract of Salvia officinalis L., negative control with 80% ethanol (v/v) and positive control of hydrogen peroxide (H2O2), t-butyl peroxide hidroxy (TBO), doxorubicin and cisplatin. Cell viability was determined by MTT reduction (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). Results were analyzed by Tukey test (p≤0,05) using the SPSS v.19. RESULTS: the hydroalcoholic extract of Salvia officinalis L. showed cytotoxic activity to tumor cells Hep-2 IC50 0,38 ± 0.02 mg/mL for HepG2 IC50 0,54 ± 0.03 mg/mL compared to negative control, staying above the IC50 obtained for their positive controls. Cisplatin showed IC50 below the extract of sage, but to obtain their IC50 was increased exposure time in six hours. CONCLUSIONS: the results of this study suggest that the extract of Salvia officinalis L. has biological activity against tumor cell; further studies are needed to confirm its efficacy and its potential role in cancer treatment. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-07-28 |
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://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790 |
url |
https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790 |
dc.language.iso.fl_str_mv |
por eng |
language |
por eng |
dc.relation.none.fl_str_mv |
https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790/8178 https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790/8179 https://revistaseletronicas.pucrs.br/scientiamedica/article/view/10790/8180 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Editora da PUCRS - ediPUCRS |
publisher.none.fl_str_mv |
Editora da PUCRS - ediPUCRS |
dc.source.none.fl_str_mv |
Scientia Medica; Vol. 22 No. 3 (2012); 131-137 Scientia Medica; v. 22 n. 3 (2012); 131-137 1980-6108 1806-5562 reponame:Scientia Medica (Porto Alegre. Online) instname:Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS) instacron:PUC_RS |
instname_str |
Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS) |
instacron_str |
PUC_RS |
institution |
PUC_RS |
reponame_str |
Scientia Medica (Porto Alegre. Online) |
collection |
Scientia Medica (Porto Alegre. Online) |
repository.name.fl_str_mv |
Scientia Medica (Porto Alegre. Online) - Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS) |
repository.mail.fl_str_mv |
scientiamedica@pucrs.br || editora.periodicos@pucrs.br |
_version_ |
1809101749627125760 |