Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29)
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1080/15287394.2015.1110067 http://hdl.handle.net/11449/165084 |
Resumo: | The dibenzylbutyrolactone lignan (-)-cubebin, which is extracted from the seeds of the pepper Piper cubeba, has shown promise as an anti-inflammatory, analgesic, leishmanicidal, antiproliferative, and trypanocidal compound. Given the therapeutic potential of (-)-cubebin, this study aimed to investigate its safety profile by analyzing cytotoxicity, mutagenicity, cell proliferation kinetics, induction of apoptosis, and expression of pro-apoptotic genes in human colon adenocarcinoma cells (HT29) exposed to (-)-cubebin. MTT cytotoxicity assays demonstrated that (-)-cubebin was cytotoxic only at 280 mu M, whereas it was not cytotoxic at 2.8, 14, or 28 mu M. Data demonstrated that (-)-cubebin was not mutagenic as evidenced by a micronucleus (MN) assay, did not alter cell-growth kinetics over 4 d, and showed absence of induced apoptosis after 24 h. Further, CASP8 and CASP9 gene expression was not markedly changed in HT29 cells exposed to 28 mu M or 70 mu M (-)-cubebin for 12 h. Based on our observations, (-)-cubebin was cytotoxic at a concentration of 280 mu M, suggesting that the use of this concentration should be avoided. However, lower concentrations exerted no apparent damaging effects, indicating that this lignan is safe to use for pharmacological purposes at certain concentrations. |
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Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29)The dibenzylbutyrolactone lignan (-)-cubebin, which is extracted from the seeds of the pepper Piper cubeba, has shown promise as an anti-inflammatory, analgesic, leishmanicidal, antiproliferative, and trypanocidal compound. Given the therapeutic potential of (-)-cubebin, this study aimed to investigate its safety profile by analyzing cytotoxicity, mutagenicity, cell proliferation kinetics, induction of apoptosis, and expression of pro-apoptotic genes in human colon adenocarcinoma cells (HT29) exposed to (-)-cubebin. MTT cytotoxicity assays demonstrated that (-)-cubebin was cytotoxic only at 280 mu M, whereas it was not cytotoxic at 2.8, 14, or 28 mu M. Data demonstrated that (-)-cubebin was not mutagenic as evidenced by a micronucleus (MN) assay, did not alter cell-growth kinetics over 4 d, and showed absence of induced apoptosis after 24 h. Further, CASP8 and CASP9 gene expression was not markedly changed in HT29 cells exposed to 28 mu M or 70 mu M (-)-cubebin for 12 h. Based on our observations, (-)-cubebin was cytotoxic at a concentration of 280 mu M, suggesting that the use of this concentration should be avoided. However, lower concentrations exerted no apparent damaging effects, indicating that this lignan is safe to use for pharmacological purposes at certain concentrations.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundacao Araucaria, BrazilUniv Estadual Londrina, BR-86057970 Londrina, Parana, BrazilUniv Estadual Paulista, Marilia, SP, BrazilUniv Estadual Paulista, Botucatu, SP, BrazilUniv Estadual Paulista, Marilia, SP, BrazilUniv Estadual Paulista, Botucatu, SP, BrazilTaylor & Francis IncUniversidade Estadual de Londrina (UEL)Universidade Estadual Paulista (Unesp)Niwa, Andressa MegumiPaula, Natalia Aparecida deVesenick, Diogo CamposSartori, DanieleMaistro, Edson Luis [UNESP]Ribeiro, Lucia Regina [UNESP]Mantovani, Mario Sergio2018-11-27T10:20:24Z2018-11-27T10:20:24Z2016-01-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article92-100application/pdfhttp://dx.doi.org/10.1080/15287394.2015.1110067Journal Of Toxicology And Environmental Health-part A-current Issues. Philadelphia: Taylor & Francis Inc, v. 79, n. 2, p. 92-100, 2016.1528-7394http://hdl.handle.net/11449/16508410.1080/15287394.2015.1110067WOS:000371183500005WOS000371183500005.pdf47875216130383150000-0003-0757-7876Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Toxicology And Environmental Health-part A-current Issues0,888info:eu-repo/semantics/openAccess2024-08-09T17:39:15Zoai:repositorio.unesp.br:11449/165084Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-09T17:39:15Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
title |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
spellingShingle |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) Niwa, Andressa Megumi |
title_short |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
title_full |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
title_fullStr |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
title_full_unstemmed |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
title_sort |
Evaluation of lignan (-)-cubebin extracted from Piper cubeba on human colon adenocarcinoma cells (HT29) |
author |
Niwa, Andressa Megumi |
author_facet |
Niwa, Andressa Megumi Paula, Natalia Aparecida de Vesenick, Diogo Campos Sartori, Daniele Maistro, Edson Luis [UNESP] Ribeiro, Lucia Regina [UNESP] Mantovani, Mario Sergio |
author_role |
author |
author2 |
Paula, Natalia Aparecida de Vesenick, Diogo Campos Sartori, Daniele Maistro, Edson Luis [UNESP] Ribeiro, Lucia Regina [UNESP] Mantovani, Mario Sergio |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Londrina (UEL) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Niwa, Andressa Megumi Paula, Natalia Aparecida de Vesenick, Diogo Campos Sartori, Daniele Maistro, Edson Luis [UNESP] Ribeiro, Lucia Regina [UNESP] Mantovani, Mario Sergio |
description |
The dibenzylbutyrolactone lignan (-)-cubebin, which is extracted from the seeds of the pepper Piper cubeba, has shown promise as an anti-inflammatory, analgesic, leishmanicidal, antiproliferative, and trypanocidal compound. Given the therapeutic potential of (-)-cubebin, this study aimed to investigate its safety profile by analyzing cytotoxicity, mutagenicity, cell proliferation kinetics, induction of apoptosis, and expression of pro-apoptotic genes in human colon adenocarcinoma cells (HT29) exposed to (-)-cubebin. MTT cytotoxicity assays demonstrated that (-)-cubebin was cytotoxic only at 280 mu M, whereas it was not cytotoxic at 2.8, 14, or 28 mu M. Data demonstrated that (-)-cubebin was not mutagenic as evidenced by a micronucleus (MN) assay, did not alter cell-growth kinetics over 4 d, and showed absence of induced apoptosis after 24 h. Further, CASP8 and CASP9 gene expression was not markedly changed in HT29 cells exposed to 28 mu M or 70 mu M (-)-cubebin for 12 h. Based on our observations, (-)-cubebin was cytotoxic at a concentration of 280 mu M, suggesting that the use of this concentration should be avoided. However, lower concentrations exerted no apparent damaging effects, indicating that this lignan is safe to use for pharmacological purposes at certain concentrations. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-01-17 2018-11-27T10:20:24Z 2018-11-27T10:20:24Z |
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.uri.fl_str_mv |
http://dx.doi.org/10.1080/15287394.2015.1110067 Journal Of Toxicology And Environmental Health-part A-current Issues. Philadelphia: Taylor & Francis Inc, v. 79, n. 2, p. 92-100, 2016. 1528-7394 http://hdl.handle.net/11449/165084 10.1080/15287394.2015.1110067 WOS:000371183500005 WOS000371183500005.pdf 4787521613038315 0000-0003-0757-7876 |
url |
http://dx.doi.org/10.1080/15287394.2015.1110067 http://hdl.handle.net/11449/165084 |
identifier_str_mv |
Journal Of Toxicology And Environmental Health-part A-current Issues. Philadelphia: Taylor & Francis Inc, v. 79, n. 2, p. 92-100, 2016. 1528-7394 10.1080/15287394.2015.1110067 WOS:000371183500005 WOS000371183500005.pdf 4787521613038315 0000-0003-0757-7876 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Toxicology And Environmental Health-part A-current Issues 0,888 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
92-100 application/pdf |
dc.publisher.none.fl_str_mv |
Taylor & Francis Inc |
publisher.none.fl_str_mv |
Taylor & Francis Inc |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
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1808128138581901312 |