Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2005-2-11
pubmed:abstractText
CP-673,451 is a potent inhibitor of platelet-derived growth factor beta-receptor (PDGFR-beta) kinase- and PDGF-BB-stimulated autophosphorylation of PDGFR-beta in cells (IC(50) = 1 nmol/L) being more than 450-fold selective for PDGFR-beta versus other angiogenic receptors (e.g., vascular endothelial growth factor receptor 2, TIE-2, and fibroblast growth factor receptor 2). Multiple models have been used to evaluate in vivo activity of CP-673,451 and to understand the pharmacology of PDGFR-beta inhibition and the effect on tumor growth. These models include an ex vivo measure of PDGFR-beta phosphorylation in glioblastoma tumors, a sponge model to measure inhibition of angiogenesis, and multiple models of tumor growth inhibition. Inhibition of PDGFR-beta phosphorylation in tumors correlates with plasma and tumor levels of CP-673,451. A dose of 33 mg/kg was adequate to provide >50% inhibition of receptor for 4 hours corresponding to an EC(50) of 120 ng/mL in plasma at C(max). In a sponge angiogenesis model, CP-673,451 inhibited 70% of PDGF-BB-stimulated angiogenesis at a dose of 3 mg/kg (q.d. x 5, p.o., corresponding to 5.5 ng/mL at C(max)). The compound did not inhibit vascular endothelial growth factor- or basic fibroblast growth factor-induced angiogenesis at concentrations which inhibited tumor growth. The antitumor efficacy of CP-673,451 was evaluated in a number of human tumor xenografts grown s.c. in athymic mice, including H460 human lung carcinoma, Colo205 and LS174T human colon carcinomas, and U87MG human glioblastoma multiforme. Once-daily p.o. x 10 days dosing routinely inhibited tumor growth (ED(50) < or = 33 mg/kg). These data show that CP-673,451 is a pharmacologically selective PDGFR inhibitor, inhibits tumor PDGFR-beta phosphorylation, selectively inhibits PDGF-BB-stimulated angiogenesis in vivo, and causes significant tumor growth inhibition in multiple human xenograft models.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0008-5472
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
957-66
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15705896-Angiogenesis Inhibitors, pubmed-meshheading:15705896-Animals, pubmed-meshheading:15705896-Antineoplastic Agents, pubmed-meshheading:15705896-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:15705896-Benzimidazoles, pubmed-meshheading:15705896-Cell Growth Processes, pubmed-meshheading:15705896-Female, pubmed-meshheading:15705896-Glioblastoma, pubmed-meshheading:15705896-Humans, pubmed-meshheading:15705896-Inhibitory Concentration 50, pubmed-meshheading:15705896-Mice, pubmed-meshheading:15705896-Mice, Nude, pubmed-meshheading:15705896-Neovascularization, Pathologic, pubmed-meshheading:15705896-Paclitaxel, pubmed-meshheading:15705896-Phosphorylation, pubmed-meshheading:15705896-Platelet-Derived Growth Factor, pubmed-meshheading:15705896-Protein Kinase Inhibitors, pubmed-meshheading:15705896-Quinolines, pubmed-meshheading:15705896-Rats, pubmed-meshheading:15705896-Receptor, Platelet-Derived Growth Factor alpha, pubmed-meshheading:15705896-Receptor, Platelet-Derived Growth Factor beta, pubmed-meshheading:15705896-Xenograft Model Antitumor Assays
pubmed:year
2005
pubmed:articleTitle
Antiangiogenic and antitumor activity of a selective PDGFR tyrosine kinase inhibitor, CP-673,451.
pubmed:affiliation
Pfizer Oncology, Pfizer Global Research and Development, Eastern Point Road, Groton, CT 06340, USA. robertswg@groton.pfizer.com
pubmed:publicationType
Journal Article