Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.4103/pm.pm_272_17 http://hdl.handle.net/11449/185103 |
Resumo: | Background: Natural compounds with therapeutic potential have been explored as antitumoral agents, as curcumin (CUR), a substance which has activity against various tumor types and a tool used to improve the action of these compounds is the production of analogs. Objective: In this study, we investigated the antitumoral activity of AC13, a CUR analog. Materials and Methods: Cytotoxicity of AC13 and CUR for different cancer cell lines was analyzed by MTT assay after 24, and 48 h of exposure and caspases 3 and 7 enzymatic activity in CasKi and human spontaneously transformed immortal keratinocyte cell line cells was analyzed after 24 h of incubation with AC13 or CUR at 50 mu M. Results: It was observed significant viability loss only for CasKi cells after incubation with AC13. Hence, it was made a more detailed screening of the cytotoxicity for these cells and nontumoral cells incubated with AC13 or CUR, showing concentration-dependent decrease of cell viability. Posteriorly, AC13 induces increase in the caspases activity in both cell lines, being that for tumor cells this increase was greater than that unleashed by CUR. Conclusion: Therefore, AC13 triggers cell death by apoptosis in CasKi and shows greater effect than CUR for these tumor cells, suggesting to be a promising compound for the treatment of cancer and should be studied more thoroughly. |
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Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin AnalogueCancercaspasecurcumincytotoxicitysynthetic analogsBackground: Natural compounds with therapeutic potential have been explored as antitumoral agents, as curcumin (CUR), a substance which has activity against various tumor types and a tool used to improve the action of these compounds is the production of analogs. Objective: In this study, we investigated the antitumoral activity of AC13, a CUR analog. Materials and Methods: Cytotoxicity of AC13 and CUR for different cancer cell lines was analyzed by MTT assay after 24, and 48 h of exposure and caspases 3 and 7 enzymatic activity in CasKi and human spontaneously transformed immortal keratinocyte cell line cells was analyzed after 24 h of incubation with AC13 or CUR at 50 mu M. Results: It was observed significant viability loss only for CasKi cells after incubation with AC13. Hence, it was made a more detailed screening of the cytotoxicity for these cells and nontumoral cells incubated with AC13 or CUR, showing concentration-dependent decrease of cell viability. Posteriorly, AC13 induces increase in the caspases activity in both cell lines, being that for tumor cells this increase was greater than that unleashed by CUR. Conclusion: Therefore, AC13 triggers cell death by apoptosis in CasKi and shows greater effect than CUR for these tumor cells, suggesting to be a promising compound for the treatment of cancer and should be studied more thoroughly.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sao Paulo State Univ, Dept Biol, Sao Jose Do Rio Preto, SP, BrazilSao Paulo State Univ, Dept Chem, Sao Jose Do Rio Preto, SP, BrazilSao Paulo State Univ, Dept Biol, Sao Jose Do Rio Preto, SP, BrazilSao Paulo State Univ, Dept Chem, Sao Jose Do Rio Preto, SP, BrazilFAPESP: 2014/04395-2Wolters Kluwer Medknow PublicationsUniversidade Estadual Paulista (Unesp)Bortolozo Oliveira, Ana Beatriz [UNESP]Adum de Matos, Renata Prandini [UNESP]Stuqui, Bruna [UNESP]Torrezan, Guilherme Silva [UNESP]Polaquini, Carlos Roberto [UNESP]Regasini, Luis Octavio [UNESP]Calmon, Marilia de Freitas [UNESP]Rahal, Paula [UNESP]2019-10-04T12:32:42Z2019-10-04T12:32:42Z2018-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article611-616http://dx.doi.org/10.4103/pm.pm_272_17Pharmacognosy Magazine. Mumbai: Wolters Kluwer Medknow Publications, v. 14, n. 58, p. 611-616, 2018.0973-1296http://hdl.handle.net/11449/18510310.4103/pm.pm_272_17WOS:000451220800023799108236267121291656014694362400000-0001-5693-6148Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPharmacognosy Magazineinfo:eu-repo/semantics/openAccess2021-10-23T20:17:35Zoai:repositorio.unesp.br:11449/185103Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:08:50.090712Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
title |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
spellingShingle |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue Bortolozo Oliveira, Ana Beatriz [UNESP] Cancer caspase curcumin cytotoxicity synthetic analogs |
title_short |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
title_full |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
title_fullStr |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
title_full_unstemmed |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
title_sort |
Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue |
author |
Bortolozo Oliveira, Ana Beatriz [UNESP] |
author_facet |
Bortolozo Oliveira, Ana Beatriz [UNESP] Adum de Matos, Renata Prandini [UNESP] Stuqui, Bruna [UNESP] Torrezan, Guilherme Silva [UNESP] Polaquini, Carlos Roberto [UNESP] Regasini, Luis Octavio [UNESP] Calmon, Marilia de Freitas [UNESP] Rahal, Paula [UNESP] |
author_role |
author |
author2 |
Adum de Matos, Renata Prandini [UNESP] Stuqui, Bruna [UNESP] Torrezan, Guilherme Silva [UNESP] Polaquini, Carlos Roberto [UNESP] Regasini, Luis Octavio [UNESP] Calmon, Marilia de Freitas [UNESP] Rahal, Paula [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Bortolozo Oliveira, Ana Beatriz [UNESP] Adum de Matos, Renata Prandini [UNESP] Stuqui, Bruna [UNESP] Torrezan, Guilherme Silva [UNESP] Polaquini, Carlos Roberto [UNESP] Regasini, Luis Octavio [UNESP] Calmon, Marilia de Freitas [UNESP] Rahal, Paula [UNESP] |
dc.subject.por.fl_str_mv |
Cancer caspase curcumin cytotoxicity synthetic analogs |
topic |
Cancer caspase curcumin cytotoxicity synthetic analogs |
description |
Background: Natural compounds with therapeutic potential have been explored as antitumoral agents, as curcumin (CUR), a substance which has activity against various tumor types and a tool used to improve the action of these compounds is the production of analogs. Objective: In this study, we investigated the antitumoral activity of AC13, a CUR analog. Materials and Methods: Cytotoxicity of AC13 and CUR for different cancer cell lines was analyzed by MTT assay after 24, and 48 h of exposure and caspases 3 and 7 enzymatic activity in CasKi and human spontaneously transformed immortal keratinocyte cell line cells was analyzed after 24 h of incubation with AC13 or CUR at 50 mu M. Results: It was observed significant viability loss only for CasKi cells after incubation with AC13. Hence, it was made a more detailed screening of the cytotoxicity for these cells and nontumoral cells incubated with AC13 or CUR, showing concentration-dependent decrease of cell viability. Posteriorly, AC13 induces increase in the caspases activity in both cell lines, being that for tumor cells this increase was greater than that unleashed by CUR. Conclusion: Therefore, AC13 triggers cell death by apoptosis in CasKi and shows greater effect than CUR for these tumor cells, suggesting to be a promising compound for the treatment of cancer and should be studied more thoroughly. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-10-01 2019-10-04T12:32:42Z 2019-10-04T12:32:42Z |
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/10.4103/pm.pm_272_17 Pharmacognosy Magazine. Mumbai: Wolters Kluwer Medknow Publications, v. 14, n. 58, p. 611-616, 2018. 0973-1296 http://hdl.handle.net/11449/185103 10.4103/pm.pm_272_17 WOS:000451220800023 7991082362671212 9165601469436240 0000-0001-5693-6148 |
url |
http://dx.doi.org/10.4103/pm.pm_272_17 http://hdl.handle.net/11449/185103 |
identifier_str_mv |
Pharmacognosy Magazine. Mumbai: Wolters Kluwer Medknow Publications, v. 14, n. 58, p. 611-616, 2018. 0973-1296 10.4103/pm.pm_272_17 WOS:000451220800023 7991082362671212 9165601469436240 0000-0001-5693-6148 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Pharmacognosy Magazine |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
611-616 |
dc.publisher.none.fl_str_mv |
Wolters Kluwer Medknow Publications |
publisher.none.fl_str_mv |
Wolters Kluwer Medknow Publications |
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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1808128322186510336 |