The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action

Detalhes bibliográficos
Autor(a) principal: Oliveira, Cristiane Bernardes de
Data de Publicação: 2013
Outros Autores: Comunello, Lucimara Nardi, Maciel, Érica Santos, Giubel, Scheron Rathke, Bruno, Alessandra Nejar, Chiela, Eduardo Cremonese Filippi, Lenz, Guido, Gnoatto, Simone Cristina Baggio, Buffon, Andreia, Gosmann, Grace
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/267627
Resumo: Baccharis trimera is used in folk medicine as a tea for digestive and liver diseases. It possesses anti-inflammatory and antioxidant properties that are related to the presence of phenolic compounds. The aim of this work was to investigate the anti-proliferative properties of phenolic (PHE) and terpenoid (SAP) compounds from B. trimera on human cervical cancer. The treatment of SiHa cells with PHE for 24 h suppressed colony formation in a dose-dependent manner, inhibited proliferation and inhibited cell motility. Although SAP inhibited the proliferation of SiHa cells in a dose-dependent manner, it increased colony formation and did not inhibit cell motility. PHE and SAP also promoted a significant increase in lactate dehydrogenase levels in the culture medium in a dose-dependent manner, indicating a loss of cell membrane integrity. Moreover, PHE promoted necrotic cell death, whereas SAP induced apoptosis. These compounds are new anticancer prototypes due their significant anticancer activity demonstrated herein.
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spelling Oliveira, Cristiane Bernardes deComunello, Lucimara NardiMaciel, Érica SantosGiubel, Scheron RathkeBruno, Alessandra NejarChiela, Eduardo Cremonese FilippiLenz, GuidoGnoatto, Simone Cristina BaggioBuffon, AndreiaGosmann, Grace2023-11-25T03:26:27Z20131420-3049http://hdl.handle.net/10183/267627000910885Baccharis trimera is used in folk medicine as a tea for digestive and liver diseases. It possesses anti-inflammatory and antioxidant properties that are related to the presence of phenolic compounds. The aim of this work was to investigate the anti-proliferative properties of phenolic (PHE) and terpenoid (SAP) compounds from B. trimera on human cervical cancer. The treatment of SiHa cells with PHE for 24 h suppressed colony formation in a dose-dependent manner, inhibited proliferation and inhibited cell motility. Although SAP inhibited the proliferation of SiHa cells in a dose-dependent manner, it increased colony formation and did not inhibit cell motility. PHE and SAP also promoted a significant increase in lactate dehydrogenase levels in the culture medium in a dose-dependent manner, indicating a loss of cell membrane integrity. Moreover, PHE promoted necrotic cell death, whereas SAP induced apoptosis. These compounds are new anticancer prototypes due their significant anticancer activity demonstrated herein.application/pdfengMolecules. Basel, Switzerland. Vol. 18, n. 9 (Sep. 2013), p. 11022-11032Baccharis trimeraTerpenóidesCompostos fenólicosNeoplasias do colo do úteroPhenolic compoundsTerpenoidsCervical cancerNecrosisApoptosisThe inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of actionEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT000910885.pdf.txt000910885.pdf.txtExtracted Texttext/plain25366http://www.lume.ufrgs.br/bitstream/10183/267627/2/000910885.pdf.txt91fa1e4c7d3354bdc36ebb336c9fc8b2MD52ORIGINAL000910885.pdfTexto completo (inglês)application/pdf476787http://www.lume.ufrgs.br/bitstream/10183/267627/1/000910885.pdfe29f88991d945304cbffc4a3a4da91c4MD5110183/2676272023-12-06 04:24:49.429357oai:www.lume.ufrgs.br:10183/267627Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-12-06T06:24:49Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
title The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
spellingShingle The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
Oliveira, Cristiane Bernardes de
Baccharis trimera
Terpenóides
Compostos fenólicos
Neoplasias do colo do útero
Phenolic compounds
Terpenoids
Cervical cancer
Necrosis
Apoptosis
title_short The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
title_full The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
title_fullStr The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
title_full_unstemmed The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
title_sort The inhibitory effects of phenolic and terpenoid compounds from Baccharis trimera in siha cells : differences in their activity and mechanism of action
author Oliveira, Cristiane Bernardes de
author_facet Oliveira, Cristiane Bernardes de
Comunello, Lucimara Nardi
Maciel, Érica Santos
Giubel, Scheron Rathke
Bruno, Alessandra Nejar
Chiela, Eduardo Cremonese Filippi
Lenz, Guido
Gnoatto, Simone Cristina Baggio
Buffon, Andreia
Gosmann, Grace
author_role author
author2 Comunello, Lucimara Nardi
Maciel, Érica Santos
Giubel, Scheron Rathke
Bruno, Alessandra Nejar
Chiela, Eduardo Cremonese Filippi
Lenz, Guido
Gnoatto, Simone Cristina Baggio
Buffon, Andreia
Gosmann, Grace
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira, Cristiane Bernardes de
Comunello, Lucimara Nardi
Maciel, Érica Santos
Giubel, Scheron Rathke
Bruno, Alessandra Nejar
Chiela, Eduardo Cremonese Filippi
Lenz, Guido
Gnoatto, Simone Cristina Baggio
Buffon, Andreia
Gosmann, Grace
dc.subject.por.fl_str_mv Baccharis trimera
Terpenóides
Compostos fenólicos
Neoplasias do colo do útero
topic Baccharis trimera
Terpenóides
Compostos fenólicos
Neoplasias do colo do útero
Phenolic compounds
Terpenoids
Cervical cancer
Necrosis
Apoptosis
dc.subject.eng.fl_str_mv Phenolic compounds
Terpenoids
Cervical cancer
Necrosis
Apoptosis
description Baccharis trimera is used in folk medicine as a tea for digestive and liver diseases. It possesses anti-inflammatory and antioxidant properties that are related to the presence of phenolic compounds. The aim of this work was to investigate the anti-proliferative properties of phenolic (PHE) and terpenoid (SAP) compounds from B. trimera on human cervical cancer. The treatment of SiHa cells with PHE for 24 h suppressed colony formation in a dose-dependent manner, inhibited proliferation and inhibited cell motility. Although SAP inhibited the proliferation of SiHa cells in a dose-dependent manner, it increased colony formation and did not inhibit cell motility. PHE and SAP also promoted a significant increase in lactate dehydrogenase levels in the culture medium in a dose-dependent manner, indicating a loss of cell membrane integrity. Moreover, PHE promoted necrotic cell death, whereas SAP induced apoptosis. These compounds are new anticancer prototypes due their significant anticancer activity demonstrated herein.
publishDate 2013
dc.date.issued.fl_str_mv 2013
dc.date.accessioned.fl_str_mv 2023-11-25T03:26:27Z
dc.type.driver.fl_str_mv Estrangeiro
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/267627
dc.identifier.issn.pt_BR.fl_str_mv 1420-3049
dc.identifier.nrb.pt_BR.fl_str_mv 000910885
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Molecules. Basel, Switzerland. Vol. 18, n. 9 (Sep. 2013), p. 11022-11032
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