Evaluation of curcumin and cisplatin-induced DNA damage in PC12 cells by the alkaline comet assay


Autoria(s): MENDONCA, Leonardo Meneghin; SANTOS, Graciela Cristina dos; SANTOS, Raquel Alves dos; TAKAHASHI, Catarina Satie; BIANCHI, Maria de Lourdes Pires; ANTUNES, Lusania Maria Greggi
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

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.

CAPES

FAPESP (Fundacao de Pesquisa do Estado de Sao Paulo)[08/53947-7]

CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)

Identificador

HUMAN & EXPERIMENTAL TOXICOLOGY, v.29, n.8, p.635-643, 2010

0960-3271

http://producao.usp.br/handle/BDPI/20327

10.1177/0960327109358731

http://dx.doi.org/10.1177/0960327109358731

Idioma(s)

eng

Publicador

SAGE PUBLICATIONS LTD

Relação

Human & Experimental Toxicology

Direitos

restrictedAccess

Copyright SAGE PUBLICATIONS LTD

Palavras-Chave #antioxidant #antitumoral #DNA damage #antigenotoxicity #ROOT GANGLION NEURONS #HAMSTER OVARY CELLS #IN-VITRO #CHROMOSOMAL DAMAGE #OXIDATIVE STRESS #GENOTOXICITY #CHEMOTHERAPY #VIVO #IDENTIFICATION #NEUROTOXICITY #Toxicology
Tipo

article

original article

publishedVersion