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Blood ; 111(4): 2238-45, 2008 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-18025156

RESUMEN

Despite vast improvements in our understanding of cancer genetics, a large percentage of cancer cases present without knowledge of the causative genetic events. Tyrosine kinases are frequently implicated in the pathogenesis of numerous types of cancer, but identification and validation of tyrosine kinase targets in cancer can be a time-consuming process. We report the establishment of an efficient, functional screening assay using RNAi technology to directly assess and compare the effect of individually targeting each member of the tyrosine kinase family. We demonstrate that siRNA screening can identify tyrosine kinase targets containing activating mutations in Janus kinase (JAK) 3 (A572V) in CMK cells and c-KIT (V560G) in HMC1.1 cells. In addition, this assay identifies targets that do not contain mutations, such as JAK1 and the focal adhesion kinases (FAK), that are crucial to the survival of the cancer cells. This technique, with additional development, might eventually offer the potential to match specific therapies with individual patients based on a functional assay.


Asunto(s)
Leucemia Mieloide Aguda/tratamiento farmacológico , Proteínas Tirosina Quinasas/genética , Interferencia de ARN/fisiología , ARN Interferente Pequeño/genética , Anticuerpos Monoclonales/uso terapéutico , Antineoplásicos/uso terapéutico , Línea Celular Tumoral , Biblioteca de Genes , Humanos , Janus Quinasa 1/genética , Janus Quinasa 3/genética , Células K562 , Leucemia Mieloide Aguda/enzimología , Leucemia Mieloide Aguda/genética
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