Cytotoxicity and Antitumoral Activity by Apoptosis Induction of AC13: A Brominated Curcumin Analogue

Detalhes bibliográficos
Autor(a) principal: Bortolozo Oliveira, Ana Beatriz [UNESP]
Data de Publicação: 2018
Outros Autores: 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]
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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spelling 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:29462021-10-23T20:17:35Repositório 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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