dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:23:40Z
dc.date.accessioned2022-10-05T13:11:42Z
dc.date.available2014-05-20T13:23:40Z
dc.date.available2022-10-05T13:11:42Z
dc.date.created2014-05-20T13:23:40Z
dc.date.issued2010-08-01
dc.identifierHuman & Experimental Toxicology. London: Sage Publications Ltd, v. 29, n. 8, p. 635-643, 2010.
dc.identifier0960-3271
dc.identifierhttp://hdl.handle.net/11449/7184
dc.identifier10.1177/0960327109358731
dc.identifierWOS:000280408700002
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3884172
dc.description.abstractA 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.
dc.languageeng
dc.publisherSage Publications Ltd
dc.relationHuman & Experimental Toxicology
dc.relation1.840
dc.relation0,559
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectantioxidant
dc.subjectantitumoral
dc.subjectDNA damage
dc.subjectantigenotoxicity
dc.titleEvaluation of curcumin and cisplatin-induced DNA damage in PC12 cells by the alkaline comet assay
dc.typeArtigo


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