Sorafenib is a potent inhibitor of FIP1L1-PDGFRα and the imatinib-resistant FIP1L1-PDGFRα T674I mutant
Data up to Jan 2025
Total Citations Per Year
Abstract
References (24)
BAY 43-9006 Exhibits Broad Spectrum Oral Antitumor Activity and Targets the RAF/MEK/ERK Pathway and Receptor Tyrosine Kinases Involved in Tumor Progression and Angiogenesis
2004 • 3,873 citations
A small molecule–kinase interaction map for clinical kinase inhibitors
2005 • 1,854 citations
A Tyrosine Kinase Created by Fusion of thePDGFRAandFIP1L1Genes as a Therapeutic Target of Imatinib in Idiopathic Hypereosinophilic Syndrome
2003 • 1,683 citations
The idiopathic hypereosinophilic syndrome
1994 • 928 citations
Phase I Clinical and Pharmacokinetic Study of the Novel Raf Kinase and Vascular Endothelial Growth Factor Receptor Inhibitor BAY 43-9006 in Patients With Advanced Refractory Solid Tumors
2004 • 855 citations
Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases
2005 • 556 citations
Targeted Therapy for Metastatic Renal Cell Carcinoma
2006 • 437 citations
Discovery of a novel Raf kinase inhibitor.
2001 • 417 citations
CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy
2003 • 395 citations
Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness
2003 • 388 citations
Phase I safety and pharmacokinetics of BAY 43-9006 administered for 21 days on/7 days off in patients with advanced, refractory solid tumours
2005 • 328 citations
Treatment of hypereosinophilic syndrome with imatinib mesilate
2002 • 310 citations
Structure of the Kinase Domain of an Imatinib-Resistant Abl Mutant in Complex with the Aurora Kinase Inhibitor VX-680
2006 • 278 citations
PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative disease
2003 • 219 citations
Discovery of a fusion kinase in EOL-1 cells and idiopathic hypereosinophilic syndrome
2003 • 203 citations
Preclinical and clinical development of the oral multikinase inhibitor sorafenib in cancer treatment
2005 • 193 citations
Phase I Trial of Sorafenib and Gemcitabine in Advanced Solid Tumors with an Expanded Cohort in Advanced Pancreatic Cancer
2006 • 187 citations
Targeted therapy for metastatic renal cell carcinoma
2006 • 141 citations
The t(4;22)(q12;q11) in atypical chronic myeloid leukaemia fuses BCR to PDGFRA
2002 • 140 citations
Characterization of a Conserved Structural Determinant Controlling Protein Kinase Sensitivity to Selective Inhibitors
2004 • 137 citations
The small molecule tyrosine kinase inhibitor AMN107 inhibits TEL-PDGFR and FIP1L1-PDGFR in vitro and in vivo
2005 • 115 citations
The EOL-1 cell line as an in vitro model for the study of FIP1L1-PDGFRA–positive chronic eosinophilic leukemia
2003 • 87 citations
Resistance to tyrosine kinase inhibitors: Calling on extra forces
2005 • 40 citations
The idiopathic hypereosinophilic syndrome and eosinophilic leukemias.
2004 • 27 citations