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Chemosensitizer effect of cisplatin-treated bladder cancer cells by phenazine-5,10-dioxides.
Hernández, Paola; Alem, Diego; Nieves, Marcos; Cerecetto, Hugo; González, Mercedes; Martínez-López, Wilner; Lavaggi, María Laura.
Afiliação
  • Hernández P; Laboratorio de Epigenética e Inestabilidad Genómica, Instituto de Investigaciones Biológicas Clemente Estable, Montevideo, Uruguay. Electronic address: phernandez@iibce.edu.uy.
  • Alem D; Laboratorio de Epigenética e Inestabilidad Genómica, Instituto de Investigaciones Biológicas Clemente Estable, Montevideo, Uruguay.
  • Nieves M; Grupo de Química Medicinal, Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
  • Cerecetto H; Grupo de Química Medicinal, Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
  • González M; Grupo de Química Medicinal, Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
  • Martínez-López W; Laboratorio de Epigenética e Inestabilidad Genómica, Instituto de Investigaciones Biológicas Clemente Estable, Montevideo, Uruguay.
  • Lavaggi ML; Grupo de Química Medicinal, Instituto de Química Biológica, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay. Electronic address: maria.lavaggi@cur.edu.uy.
Environ Toxicol Pharmacol ; 69: 9-15, 2019 Jul.
Article em En | MEDLINE | ID: mdl-30921672
ABSTRACT
We determined the chemosensitizer effect of phenazine dioxide derivatives to cisplatin and the possible mechanism of action on bladder cancer cells. Anti-proliferative activity of nine phenazine dioxide derivatives in presence or absence of cisplatin was evaluated in two bladder tumor human cells T24 and 253 J and one non tumor cell line V79-4. The sensitizer effect of the combined treatment was determined by chromosomal aberrations and micronucleus test. A possible mechanism of action of the sensitizer compounds as HDACi was also investigated.The phenazine dioxide 2c combined with cisplatin induced a cell cycle arrest on bladder cancer cells and resensitize the invasive and cisplatin resistant 253 J cell line. The HDAC inhibitory activity appears as one of the mechanism of action of the compound. The low toxicity levels against normal cells point out the phenazine dioxide derivative 2c as a very good scaffold for further design of HDACi sensitizer agents.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenazinas / Cisplatino / Inibidores de Histona Desacetilases / Antineoplásicos Limite: Humans Idioma: En Revista: Environ Toxicol Pharmacol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenazinas / Cisplatino / Inibidores de Histona Desacetilases / Antineoplásicos Limite: Humans Idioma: En Revista: Environ Toxicol Pharmacol Ano de publicação: 2019 Tipo de documento: Article