Discovery of a Novel Inhibitor of the Protein Tyrosine Phosphatase Shp2

被引:45
作者
Chen, Chuan [1 ]
Cao, Mengmeng [1 ]
Zhu, Siyu [1 ]
Wang, Cuicui [1 ]
Liang, Fan [1 ]
Yan, Leilei [1 ]
Luo, Duqiang [1 ]
机构
[1] Hebei Univ, Minist Educ, Key Lab Med Chem & Mol Diag, Coll Life Sci, Baoding 071002, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
BREAST-CANCER; KINASE-ACTIVITY; ACTIVATION; GAB1; RAS; SRC; PTPN11; FAMILY; EXPRESSION; PAXILLIN;
D O I
10.1038/srep17626
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Shp2 is a ubiquitously expressed protein tyrosine phosphatase (PTP) related to adult acute myelogenous leukemia and human solid tumors. In this report, we describe identification of a potent Shp2 inhibitor, Fumosorinone (Fumos) from entomogenous fungi, which shows selective inhibition of Shp2 over other tested PTPs. Using a surface plasmon resonance analysis, we further confirmed the physical interaction between Shp2 and Fumos. Fumos inhibits Shp2-dependent activation of the Ras/ERK signal pathway downstream of EGFR, and interrupts EGF-induced Gab1-Shp2 association. As expected, Fumos shows little effects on the Shp2-independent ERK1/2 activation induced by PMA or oncogenic Ras. Furthermore, Fumos down-regulates Src activation, inhibits phosphorylation of Paxillin and prevents tumor cell invasion. These results suggest that Fumos can inhibit Shp2-dependent cell signaling in human cells and has a potential for treatment of Shp2-associated diseases.
引用
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页数:13
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