The Tyr-kinase inhibitor AG879, that blocks the ETK-PAK1 interaction, suppresses the RAS-induced PAK1 activation and malignant transformation

He, H; Hirokawa, Y; Gazit, A; Yamashita, Y; Mano, H; Kawakami, Y; Kawakami; Hsieh, CY; Kung, HJ; Lessene, G; Baell, J; Levitzki, A; Maruta, H

Author(s): He, H; Hirokawa, Y; Gazit, A; Yamashita, Y; Mano, H; Kawakami, Y; Kawakami; Hsieh, CY; Kung, HJ; Lessene, G; Baell, J; Levitzki, A; Maruta, H;
Details: Publication Year 2004-01,Volume 3,Issue #1,Page 96-101
Journal Title: CANCER BIOLOGY & THERAPY
Publication Type: Journal Article
Abstract: AG 879 has been widely used as a Tyr kinase inhibitor specific for ErbB2 and FLK-1, a VEGF receptor. The IC50 for both ErbB2 and FLK-1 is around 1 muM. AG 879, in combination of PP1 (an inhibitor specific for Src kinase family), suppresses almost completely the growth of RAS-induced sarcomas in nude mice. In this paper we demonstrate that AG 879 even at 10 nM blocks the specific interaction between the Tyr-kinase ETK and PAK1 (a CDC42/ Rac-dependent Ser/Thr kinase) in cell culture. This interaction is essential for both the RAS-induced PAK1 activation and transformation of NIH 3T3 fibroblasts. However, AG 879 at 10 nM does not inhibit either the purified ETK or PAK1 directly in vitro, suggesting that this drug blocks the ETK-PAK1 pathway by targeting a highly sensitive kinase upstream of ETK. Although the Tyr-kinases Src and FAK are known to activate ETK directly, Src is insensitive to AG 879, and FAK is inhibited by 100 nM AG 879, but not by 10 nM AG879. The structure-function relationship analysis of AG 879 derivatives has revealed that both thio and tert-butyl groups of AG 879, but not (thio) amide group, are essential for its biological function (blocking the ETK-PAK1 pathway), suggesting that through the (thio) amide group, AG 879 can be covalently linked to agarose beads to form a bioactive affinity ligand useful for identifying the primary target of this drug.
Publisher: LANDES BIOSCIENCE
Keywords: GROWTH-FACTOR RECEPTOR; FOCAL ADHESION KINASE; SRC FAMILY KINASES; TYROSINE KINASE; CANCER CELLS; FERM DOMAIN; IN-VITRO; PROTEINS; BTK; ETK/BMX
Publisher's Version: https://doi.org/10.4161/cbt.3.1.643
Terms of Use/Rights Notice: Refer to copyright notice on published article.

Creation Date: 2004-01-01 12:00:00