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

Hong He, Yumiko Hirokawa, Aviv Gazit, Yoshihiro Yamashita, Hiroyuki Mano, Yuko Kawakami, Kawakami, Ching Yi Hsieh, Hsing Jien Kung, Guillaume Lessene, Jonathan Baell, Alexander Levitzki, Hiroshi Maruta

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

AG 879 has been widely used as a Tyr kinase inhibitor specific for ErbB2 and FIK-1, a VEGF receptor. The IC50 for both ErbB2 and FIK-1 is around 1 μM. 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 notby 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.

Original languageEnglish
Pages (from-to)96-101
Number of pages6
JournalCancer Biology and Therapy
Volume3
Issue number1
Publication statusPublished - Jan 1 2004
Externally publishedYes

Keywords

  • AG879
  • ETK
  • PAK
  • RAS
  • Transformation

ASJC Scopus subject areas

  • Molecular Medicine
  • Oncology
  • Pharmacology
  • Cancer Research

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  • Cite this

    He, H., Hirokawa, Y., Gazit, A., Yamashita, Y., Mano, H., Kawakami, Y., Kawakami, Hsieh, C. Y., Kung, H. J., Lessene, G., Baell, J., Levitzki, A., & Maruta, H. (2004). The Tyr-kinase inhibitor AG879, that blocks the ETK-PAK1 interaction, suppresses the RAS-induced PAK1 activation and malignant transformation. Cancer Biology and Therapy, 3(1), 96-101.