1. Academic Validation
  2. Discovery of a novel shp2 protein tyrosine phosphatase inhibitor

Discovery of a novel shp2 protein tyrosine phosphatase inhibitor

  • Mol Pharmacol. 2006 Aug;70(2):562-70. doi: 10.1124/mol.106.025536.
Liwei Chen 1 Shen-Shu Sung M L Richard Yip Harshani R Lawrence Yuan Ren Wayne C Guida Said M Sebti Nicholas J Lawrence Jie Wu
Affiliations

Affiliation

  • 1 Molecular Oncology Program, SRB-3, H. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA.
Abstract

SHP2 is a nonreceptor protein tyrosine Phosphatase (PTP) encoded by the PTPN11 gene. It is involved in growth factorinduced activation of mitogen-activated protein (MAP) kinases ERK1 and ERK2 (ERK1/2) and has been implicated in the pathogenicity of the oncogenic bacterium Helicobacter pylori. Moreover, gain-of-function SHP2 mutations have been found in childhood leukemias and Noonan syndrome. Thus, small molecule SHP2 PTP inhibitors are much needed reagents for evaluation of SHP2 as a therapeutic target and for chemical biology studies of SHP2 function. By screening the National Cancer Institute (NCI) Diversity Set chemical library, we identified 8-hydroxy-7-(6-sulfonaphthalen-2-yl)diazenyl-quinoline-5-sulfonic acid (NSC-87877) as a potent SHP2 PTP inhibitor. Molecular modeling and site-directed mutagenesis studies suggested that NSC-87877 binds to the catalytic cleft of SHP2 PTP. NSC-87877 cross-inhibited Shp1 in vitro, but it was selective for SHP2 over other PTPs (PTP1B, HePTP, DEP1, CD45, and LAR). It is noteworthy that NSC-87877 inhibited epidermal growth factor (EGF)-induced activation of SHP2 PTP, Ras, and ERK1/2 in cell cultures but did not block EGF-induced Gab1 tyrosine phosphorylation or Gab1-Shp2 association. Furthermore, NSC-87877 inhibited ERK1/2 activation by a Gab1-Shp2 chimera but did not affect the Shp2-independent ERK1/2 activation by phorbol 12-myristate 13-acetate. These results identified NSC-87877 as the first PTP inhibitor capable of inhibiting SHP2 PTP in cell cultures without a detectable off-target effect. Our study also provides the first pharmacological evidence that SHP2 mediates EGF-induced ERK1/2 MAP kinase activation.

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