Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions

Detalhes bibliográficos
Autor(a) principal: Aquino, I. [UNESP]
Data de Publicação: 2013
Outros Autores: Tsuboy, M. S F [UNESP], Marcarini, J. C. [UNESP], Mantovani, M. S., Perazzo, F. F., Maistro, Edson Luis [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.4238/2013.July.24.6
http://hdl.handle.net/11449/76047
Resumo: The malaria treatment recommended by the World Health Organization involves medicines derived from artemisinin, an active compound extracted from the plant Artemisia annua, and some of its derivatives, such as artesunate. Considering the lack of data regarding the genotoxic effects of these compounds in human cells, the objective of this study was to evaluate the cytotoxicity and genotoxicity, and expressions of the CASP3 and SOD1 genes in a cultured human hepatocellular liver carcinoma cell line (HepG2 cells) treated with artemisinin and artesunate. We tested concentrations of 2.5, 5, 7.5, 10, and 20 μg/mL of both substances with a resazurin cytotoxicity assay, and the concentrations used in the genotoxicity experiments (2.5, 5, and 10 μg/mL) and gene expression analysis (5 mg/mL) were determined. The results of the comet assay in cells treated with artemisinin and artesunate showed a significant dosedependent increase (P < 0.001) in the number of cells with DNA damage at all concentrations tested. However, the gene expression analysis revealed no significant change in expression of CASP3 or SOD1. Our data showed that although artemisinin and artesunate exhibited genotoxic effects in cultured HepG2 cells, they did not significantly alter expression of the CASP3 and SOD1 genes at the doses tested. ©FUNPEC-RP.
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spelling Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressionsArtemisininArtesunateCASP3 and SOD1 genesComet assayGene expressionHepG2 cellsartemisininartesunatecaspase 3cell DNAdoxorubicinextracellular superoxide dismutaseresazurinCasp3 genecell countcell strain HepG2comet assayconcentration responsecontrolled studycytotoxicityDNA damagedrug effectdrug screeninggene expressiongenotoxicityhumanhuman cellSOD1 geneThe malaria treatment recommended by the World Health Organization involves medicines derived from artemisinin, an active compound extracted from the plant Artemisia annua, and some of its derivatives, such as artesunate. Considering the lack of data regarding the genotoxic effects of these compounds in human cells, the objective of this study was to evaluate the cytotoxicity and genotoxicity, and expressions of the CASP3 and SOD1 genes in a cultured human hepatocellular liver carcinoma cell line (HepG2 cells) treated with artemisinin and artesunate. We tested concentrations of 2.5, 5, 7.5, 10, and 20 μg/mL of both substances with a resazurin cytotoxicity assay, and the concentrations used in the genotoxicity experiments (2.5, 5, and 10 μg/mL) and gene expression analysis (5 mg/mL) were determined. The results of the comet assay in cells treated with artemisinin and artesunate showed a significant dosedependent increase (P < 0.001) in the number of cells with DNA damage at all concentrations tested. However, the gene expression analysis revealed no significant change in expression of CASP3 or SOD1. Our data showed that although artemisinin and artesunate exhibited genotoxic effects in cultured HepG2 cells, they did not significantly alter expression of the CASP3 and SOD1 genes at the doses tested. ©FUNPEC-RP.Instituto de Biociências Universidade Estadual Paulista, Botucatu, SPInstituto de Biociências Universidade Estadual Paulista, Rio Claro, SPLaboratório de Genética Toxicológica Universidade Estadual de Londrina, Londrina, PRDepartamento de Ciências Exatas e da Terra Universidade Federal de São Paulo, Diadema, SPDepartamento de Fonoaudiologia Universidade Estadual Paulista, Marília, SPInstituto de Biociências Universidade Estadual Paulista, Botucatu, SPInstituto de Biociências Universidade Estadual Paulista, Rio Claro, SPDepartamento de Fonoaudiologia Universidade Estadual Paulista, Marília, SPUniversidade Estadual Paulista (Unesp)Universidade Estadual de Londrina (UEL)Universidade Federal de São Paulo (UNIFESP)Aquino, I. [UNESP]Tsuboy, M. S F [UNESP]Marcarini, J. C. [UNESP]Mantovani, M. S.Perazzo, F. F.Maistro, Edson Luis [UNESP]2014-05-27T11:30:02Z2014-05-27T11:30:02Z2013-07-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2517-2527application/pdfhttp://dx.doi.org/10.4238/2013.July.24.6Genetics and Molecular Research, v. 12, n. 3, p. 2517-2527, 2013.1676-5680http://hdl.handle.net/11449/7604710.4238/2013.July.24.6WOS:0003317174000352-s2.0-848808146502-s2.0-84880814650.pdf47875216130383150000-0003-0757-7876Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengGenetics and Molecular Research0,439info:eu-repo/semantics/openAccess2024-08-09T17:39:15Zoai:repositorio.unesp.br:11449/76047Repositório 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 Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
title Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
spellingShingle Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
Aquino, I. [UNESP]
Artemisinin
Artesunate
CASP3 and SOD1 genes
Comet assay
Gene expression
HepG2 cells
artemisinin
artesunate
caspase 3
cell DNA
doxorubicin
extracellular superoxide dismutase
resazurin
Casp3 gene
cell count
cell strain HepG2
comet assay
concentration response
controlled study
cytotoxicity
DNA damage
drug effect
drug screening
gene expression
genotoxicity
human
human cell
SOD1 gene
title_short Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
title_full Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
title_fullStr Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
title_full_unstemmed Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
title_sort Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
author Aquino, I. [UNESP]
author_facet Aquino, I. [UNESP]
Tsuboy, M. S F [UNESP]
Marcarini, J. C. [UNESP]
Mantovani, M. S.
Perazzo, F. F.
Maistro, Edson Luis [UNESP]
author_role author
author2 Tsuboy, M. S F [UNESP]
Marcarini, J. C. [UNESP]
Mantovani, M. S.
Perazzo, F. F.
Maistro, Edson Luis [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Londrina (UEL)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Aquino, I. [UNESP]
Tsuboy, M. S F [UNESP]
Marcarini, J. C. [UNESP]
Mantovani, M. S.
Perazzo, F. F.
Maistro, Edson Luis [UNESP]
dc.subject.por.fl_str_mv Artemisinin
Artesunate
CASP3 and SOD1 genes
Comet assay
Gene expression
HepG2 cells
artemisinin
artesunate
caspase 3
cell DNA
doxorubicin
extracellular superoxide dismutase
resazurin
Casp3 gene
cell count
cell strain HepG2
comet assay
concentration response
controlled study
cytotoxicity
DNA damage
drug effect
drug screening
gene expression
genotoxicity
human
human cell
SOD1 gene
topic Artemisinin
Artesunate
CASP3 and SOD1 genes
Comet assay
Gene expression
HepG2 cells
artemisinin
artesunate
caspase 3
cell DNA
doxorubicin
extracellular superoxide dismutase
resazurin
Casp3 gene
cell count
cell strain HepG2
comet assay
concentration response
controlled study
cytotoxicity
DNA damage
drug effect
drug screening
gene expression
genotoxicity
human
human cell
SOD1 gene
description The malaria treatment recommended by the World Health Organization involves medicines derived from artemisinin, an active compound extracted from the plant Artemisia annua, and some of its derivatives, such as artesunate. Considering the lack of data regarding the genotoxic effects of these compounds in human cells, the objective of this study was to evaluate the cytotoxicity and genotoxicity, and expressions of the CASP3 and SOD1 genes in a cultured human hepatocellular liver carcinoma cell line (HepG2 cells) treated with artemisinin and artesunate. We tested concentrations of 2.5, 5, 7.5, 10, and 20 μg/mL of both substances with a resazurin cytotoxicity assay, and the concentrations used in the genotoxicity experiments (2.5, 5, and 10 μg/mL) and gene expression analysis (5 mg/mL) were determined. The results of the comet assay in cells treated with artemisinin and artesunate showed a significant dosedependent increase (P < 0.001) in the number of cells with DNA damage at all concentrations tested. However, the gene expression analysis revealed no significant change in expression of CASP3 or SOD1. Our data showed that although artemisinin and artesunate exhibited genotoxic effects in cultured HepG2 cells, they did not significantly alter expression of the CASP3 and SOD1 genes at the doses tested. ©FUNPEC-RP.
publishDate 2013
dc.date.none.fl_str_mv 2013-07-24
2014-05-27T11:30:02Z
2014-05-27T11:30:02Z
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/10.4238/2013.July.24.6
Genetics and Molecular Research, v. 12, n. 3, p. 2517-2527, 2013.
1676-5680
http://hdl.handle.net/11449/76047
10.4238/2013.July.24.6
WOS:000331717400035
2-s2.0-84880814650
2-s2.0-84880814650.pdf
4787521613038315
0000-0003-0757-7876
url http://dx.doi.org/10.4238/2013.July.24.6
http://hdl.handle.net/11449/76047
identifier_str_mv Genetics and Molecular Research, v. 12, n. 3, p. 2517-2527, 2013.
1676-5680
10.4238/2013.July.24.6
WOS:000331717400035
2-s2.0-84880814650
2-s2.0-84880814650.pdf
4787521613038315
0000-0003-0757-7876
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Genetics and Molecular Research
0,439
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 2517-2527
application/pdf
dc.source.none.fl_str_mv Scopus
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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