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Biochem Biophys Res Commun ; 378(3): 650-5, 2009 Jan 16.
Artigo em Inglês | MEDLINE | ID: mdl-19059207

RESUMO

The extracellular signal-regulated kinase (ERK) signaling pathway is constitutively activated in many human tumor cell types. Given the cytoprotective role of this pathway, we examined whether its specific blockade might sensitize human tumor cells to the induction of apoptosis by various anticancer drugs. Although blockade of ERK signaling alone did not induce substantial cell death, it resulted in marked and selective enhancement of the induction of apoptosis by microtubule-destabilizing agents in tumor cells in which the ERK pathway is constitutively activated. The synergistic activation of c-Jun NH(2)-terminal kinase by the combination of an ERK pathway inhibitor and a microtubule-destabilizing agent appeared to be responsible, at least in part, for this effect. These results suggest that administration of the combination of an ERK pathway inhibitor and a microtubule-destabilizing agent is a potential chemotherapeutic strategy for the treatment of tumor cells with constitutive activation of the ERK pathway.


Assuntos
Apoptose , MAP Quinases Reguladas por Sinal Extracelular/antagonistas & inibidores , Microtúbulos/efeitos dos fármacos , Neoplasias/enzimologia , Inibidores de Proteínas Quinases/farmacologia , Moduladores de Tubulina/farmacologia , Linhagem Celular Tumoral , Flavonoides/farmacologia , Humanos , Vincristina/farmacologia
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