Author/Authors :
Celia Dominguez، نويسنده , , Leon Smith II، نويسنده , , Qi Huang، نويسنده , , Chester Yuan، نويسنده , , Xiaohu Ouyang، نويسنده , , Lynn Cai، نويسنده , , Paul Chen، نويسنده , , Joseph Kim، نويسنده , , Timothy Harvey، نويسنده , , Rashid Syed، نويسنده , , Tae-Seong Kim، نويسنده , , Andrew Tasker، نويسنده , , Ling Wang، نويسنده , , Michael Zhang، نويسنده , , Angela Coxon، نويسنده , , James Bready، نويسنده , , Charles Starnes، نويسنده , , Danlin Chen، نويسنده , , Yongmei Gan، نويسنده , , Sesha Neervannan، نويسنده , , et al.، نويسنده ,
Abstract :
Inhibition of tumor-induced angiogenesis is a promising strategy in anticancer research. Neovascularization is a process required for both tumor growth and metastasis. Enhanced understanding of the underlying molecular mechanisms has led to the discovery of a variety of pharmaceutically attractive targets. Decades of investigation suggest that vascular endothelial growth factor (VEGF) and its receptors, in particular VEGFR2 or kinase insert-domain-containing receptor (Kdr), play a critical role in the growth and survival of endothelial cells in newly forming vasculature. The clinical utility of inhibitors of this receptor tyrosine kinase is currently under intense investigation. Herein we report our efforts in this arena.
Keywords :
VEGF , VEGFR-2 inhibitor , kinase inhibitor , Kdr inhibitor , Angiogenesis inhibitor