Comparison of staurosporine and four analogues: their effects on growth, rhodamine 123 retention and binding to P-glycoprotein in multidrug-resistant MCF-7/Adr cells.

The potent kinase inhibitor staurosporine and its protein kinase C (PKC)-selective analogue CGP 41251 are known to sensitise cells with the multidrug resistance (MDR) phenotype mediated by P-glycoprotein (P-gp) to cytotoxic agents. Here four PKC-selective staurosporine cogeners, CGP 41251, UCN-01, R...

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Detalles Bibliográficos
Autores principales: Budworth, J., Davies, R., Malkhandi, J., Gant, T. W., Ferry, D. R., Gescher, A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1996
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074394/
https://www.ncbi.nlm.nih.gov/pubmed/8624264

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074394/
https://www.ncbi.nlm.nih.gov/pubmed/8624264

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