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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/7184
Título: 
Evaluation of curcumin and cisplatin-induced DNA damage in PC12 cells by the alkaline comet assay
Autor(es): 
Instituição: 
  • Universidade de São Paulo (USP)
  • Universidade Estadual Paulista (UNESP)
ISSN: 
0960-3271
Financiador: 
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Número do financiamento: 
FAPESP: 08/53947-7
Resumo: 
A very appropriate method for antigenotoxicity evaluation of antioxidants is the comet assay, since this analytical method detects initial DNA lesions that are still subject to repair; in other words, lesions that are very associated to damages resulting from the generation and subsequent action of reactive species. However, a solid evaluation should be developed in order to avoid inexact interpretations. In our study, besides the association of curcumin with cisplatin, curcumin and cisplatin agents were also tested separately. Classical genotoxic compounds, when tested by the comet assay, present an increase in the nucleoid tail; however, the cisplatin treatment has resulted in a decrease of DNA migration. This was an expected effect, as the cross-links between cisplatin and DNA decrease the DNA electrophoretic mobility. A similar effect was observed with the curcumin treatment, which decreased the nucleoid tail. Such effect was not expected and reinforced the necessity of including in the study, separate treatment groups with potentially antigenotoxic substances. The comet assay results have been analyzed using specific software for image analysis, as well as the classical visual analysis, and we have observed that the effect of decrease in DNA electrophoretic mobility was more easily observed when the data were analyzed by the software.
Data de publicação: 
1-Ago-2010
Citação: 
Human & Experimental Toxicology. London: Sage Publications Ltd, v. 29, n. 8, p. 635-643, 2010.
Duração: 
635-643
Publicador: 
Sage Publications Ltd
Palavras-chaves: 
  • antioxidant
  • antitumoral
  • DNA damage
  • antigenotoxicity
Fonte: 
http://dx.doi.org/10.1177/0960327109358731
Endereço permanente: 
Direitos de acesso: 
Acesso restrito
Tipo: 
outro
Fonte completa:
http://repositorio.unesp.br/handle/11449/7184
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