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dc.contributor.authorOliveira, Diêgo Madureira de-
dc.contributor.authorLima, Rute Maria Ferreira-
dc.contributor.authorVelozo, Jorge Clarencio de Eudes da Silva-
dc.contributor.authorAmorim, Ilza Alves de-
dc.contributor.authorMota, Tales Henrique Andrade da-
dc.contributor.authorCosta, Silvia Lima-
dc.contributor.authorPittella-Silva, Fabio-
dc.contributor.authorEl-Bachá, Ramon dos Santos-
dc.date.accessioned2022-10-04T12:37:14Z-
dc.date.available2022-10-04T12:37:14Z-
dc.date.issued2016-
dc.identifier.citationOLIVEIRA, Diêgo Madureira de et al. The classical photoactivated drug 8-methoxypsoralen and related compounds are effective without UV light irradiation against glioma cells. Neurochemistry International, v. 99, p. 33-41, out. 2016. DOI: https://doi.org/10.1016/j.neuint.2016.06.004.pt_BR
dc.identifier.urihttps://repositorio.unb.br/handle/10482/44979-
dc.language.isoInglêspt_BR
dc.publisherElsevierpt_BR
dc.rightsAcesso Restritopt_BR
dc.titleThe classical photoactivated drug 8-methoxypsoralen and related compounds are effective without UV light irradiation against glioma cellspt_BR
dc.typeArtigopt_BR
dc.subject.keywordGliomapt_BR
dc.subject.keywordMedicamentospt_BR
dc.identifier.doihttps://doi.org/10.1016/j.neuint.2016.06.004pt_BR
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0197018616301498?via%3Dihubpt_BR
dc.description.abstract1Currently, there is no effective therapy for high grade gliomas. 8-Methoxypsoralen (8-MOP) is a compound used in the treatment of skin diseases combined with UV light irradiation. In this work, rat glioma C6 cells, normal astrocytes and human glioblastoma GL-15 cells comprised an in vitro model to evaluate the antitumor activity of 8-MOP. We found that 8-MOP promoted a time- and concentration-dependent reduction of cell viability in tumor, but not in normal cells. This effect was more evident in log-phase growing culture, indicating antiproliferative activity, which was confirmed by colony formation assay. Long-term effect of 8-MOP at low concentration was also attested. The concentrations used in the tests (0.02–0.4 mM) were lower than plasmatic concentration found in patients. Despite the treatment leads to considerable morphological changes and apoptosis when used at high concentrations, 8-MOP did not promote cell cycle arrest, change in migration pattern neither necrosis. In addition, we evaluated the effect of 8-MOP in MDA-MB-231, CT-26 and SCC-3 cell lines, derived from other kind of primary tumors, and found that CT-26 cells did not respond to 8-MOP treatment, indicating that this compound does not act through a generic mechanism. Coumarin derivatives structurally related to 8-MOP were screened for its antitumor potential and presented different patterns of biological activity, and then it was possible to suggest the relevance of 8-MOP molecular structure for antiproliferative action. Therefore, 8-MOP, a drug with an outstanding record of safety, and related coumarins are good prototypes for development of a new class of anti-glioma drugs.pt_BR
dc.contributor.affiliationUniversidade de Brasília, Faculdade UnB Ceilândiapt_BR
dc.contributor.affiliationUniversidade de Brasília, Faculdade de Ciências da Saúde, Laboratório de Patologia Molecular do Câncerpt_BR
dc.contributor.affiliationUniversidade Federal da Bahia,Instituto de Ciências da Saúde, Laboratório de Neuroquímica e Biologia Celularpt_BR
dc.contributor.affiliationFiocruz, Centro de Pesquisa Gonçalo Moniz, Bahiapt_BR
dc.contributor.affiliationEscola de Medicina e Saúde Pública da Bahiapt_BR
dc.contributor.affiliationUniversidade Federal da Bahia, Faculdade de Farmácia, LAPEMMpt_BR
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