Artículos de revistas
BCR-ABL binds to IRS-1 and IRS-1 phosphorylation is inhibited by imatinib in K562 cells
Registro en:
Febs Letters. Elsevier Science Bv, v. 535, n. 41699, n. 17, n. 22, 2003.
0014-5793
WOS:000180734900005
10.1016/S0014-5793(02)03845-0
Autor
Traina, F
Carvalheira, JBC
Saad, MJA
Costa, FF
Saad, STO
Institución
Resumen
In the present study we used K562 cells to demonstrate that insulin receptor substrate 1 (IRS-1) is expressed and constitutively phosphorylated in BCR-ABL(+) cells. We observed association between BCR-ABL/IRS-1, IRS-1/phosphoinositide 3'-kinase (PI3-kinase), and IRS-1/Grb2 in the K562 cell line. Our findings demonstrate that imatinib treatment resulted in marked attenuation of BCR-ABL/IRS-1 association and of IRS-1-stimulated PI3-kinase activity in K562 cells. We concluded that the IRS-1 protein is involved in the signalling pathway of the BCR-ABL tyrosine kinase. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved. 535 41699 17 22