Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , |
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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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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1808128138588192768 |