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Oncogene ; 22(5): 660-4, 2003 Feb 06.
Artículo en Inglés | MEDLINE | ID: mdl-12569358

RESUMEN

Systemic mastocytosis (SM) is a rare disease caused by an abnormal mast cell accumulation in various tissues. Two classes of constitutive activating c-kit mutations are found in SM. The most frequent class occurs in the catalytic pocket coding region with substitutions at codon 816 and the other in the intracellular juxtamembrane coding region. Therefore, kinase inhibitors that block mutated c-kit activity might be used as therapeutic agents in SM. Here, we show that STI571 inhibits both wild-type and juxtamembrane mutant c-kit kinase activity, but has no effect on the activity of the D816 V mutant. Accordingly, STI571 selectively decreases the survival of normal mast cell and of mast cell lines either with juxtamembrane c-kit mutations, but not that of tumoral mast cell from patient with SM or of mast cell lines with the D816 V mutation. Therefore, STI571 is not a good candidate to treat SM and specific kinase inhibitors should be designed to inhibit constitutive activating mutations at codon 816.


Asunto(s)
Antineoplásicos/farmacología , Inhibidores Enzimáticos/farmacología , Mastocitosis Sistémica/tratamiento farmacológico , Piperazinas/farmacología , Proteínas Proto-Oncogénicas c-kit/efectos de los fármacos , Proteínas Proto-Oncogénicas c-kit/genética , Pirimidinas/farmacología , Benzamidas , Dominio Catalítico/genética , Línea Celular , Humanos , Mesilato de Imatinib , Mastocitosis Sistémica/genética , Proteínas Tirosina Quinasas/antagonistas & inhibidores , Relación Estructura-Actividad
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