Genotoxic evaluation of the antimalarial drugs artemisinin and artesunate in human HepG2 cells and effects on CASP3 and SOD1 gene expressions
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Data
2013-07-24
Autores
Aquino, I. [UNESP]
Tsuboy, M. S F [UNESP]
Marcarini, J. C. [UNESP]
Mantovani, M. S.
Perazzo, F. F.
Maistro, Edson Luis [UNESP]
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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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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
Como citar
Genetics and Molecular Research, v. 12, n. 3, p. 2517-2527, 2013.