reviewJournal of Clinical OncologyFeb 27, 2007Closed access

Sunitinib: From Rational Design to Clinical Efficacy

University of Colorado Health · University of Colorado Anschutz Medical Campus

PubMed
Indexed incrossrefpubmed

Abstract

Sunitinib (SU011248) is an oral small molecular tyrosine kinase inhibitor that exhibits potent antiangiogenic and antitumor activity. Tyrosine kinase inhibitors such as SU6668 and SU5416 (semaxanib) demonstrated poor pharmacologic properties and limited efficacy; therefore, sunitinib was rationally designed and chosen for its high bioavailability and its nanomolar-range potency against the antiangiogenic receptor tyrosine kinases (RTKs)--vascular endothelial growth factor receptor (VEGFR) and platelet-derived growth factor receptor (PDGFR). Sunitinib inhibits other tyrosine kinases including, KIT, FLT3, colony-stimulating factor 1 (CSF-1), and RET, which are involved in a number of malignancies including…

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877
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FWCI
37.52
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100%
References
103
Citations per year

Authors

2

Topics & keywords

Keywords
  • Sunitinib
  • Medicine
  • Tyrosine-kinase inhibitor
  • Cancer research
  • Erlotinib
  • Tyrosine kinase
  • Receptor tyrosine kinase
  • Platelet-derived growth factor receptor
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