Abstract
Receptor tyrosine kinases (RTKs) modulate a variety of cellular events, including cell proliferation, differentiation, mobility and apoptosis. In addition, RTKs have been validated as targets for cancer therapies. Microtubules are another class of proven targets for many clinical anticancer drugs. Here, we report that 1-(4-chloro-3-(trifluoromethyl) phenyl)-3-(2-cyano-4-hydroxyphenyl)urea (D181) functions as both a receptor tyrosine kinase inhibitor and a tubulin polymerization enhancer. D181 displayed potent inhibitory activities against a panel of RTKs, including Flt3, VEGFR, cKit, FGFR1 and PDGFRβ. D181 also enhanced tubulin polymerization and modified the secondary structure of tubulin proteins to disrupt their dynamic instability. Because of synergistic cooperation, D181 strongly inhibited the proliferation of various cancer cell lines, induced LoVo cell cycle arrest in the G1 and M phases and suppressed tumor growth in nude mice bearing human LoVo and HT29 xenografts. Our studies have provided a new, promising lead compound and novel clues for multi-target anticancer drug design and development.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / pharmacology*
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Apoptosis / drug effects
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Binding Sites
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Cell Cycle Proteins / metabolism
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Cell Proliferation / drug effects
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Dose-Response Relationship, Drug
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ErbB Receptors / antagonists & inhibitors
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ErbB Receptors / metabolism
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G1 Phase Cell Cycle Checkpoints / drug effects*
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HT29 Cells
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HeLa Cells
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Hep G2 Cells
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Human Umbilical Vein Endothelial Cells / drug effects
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Human Umbilical Vein Endothelial Cells / enzymology
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Human Umbilical Vein Endothelial Cells / pathology
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Humans
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Inhibitory Concentration 50
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M Phase Cell Cycle Checkpoints / drug effects*
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Male
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Mice
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Mice, Inbred BALB C
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Mice, Nude
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Microtubules / drug effects*
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Microtubules / metabolism
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Models, Molecular
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Molecular Sequence Data
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NIH 3T3 Cells
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Neoplasms / blood supply
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Neoplasms / drug therapy*
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Neoplasms / enzymology
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Neoplasms / pathology
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Neovascularization, Pathologic / enzymology
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Neovascularization, Pathologic / prevention & control
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Phenylurea Compounds / chemistry
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Phenylurea Compounds / pharmacology*
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Phosphorylation
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Protein Conformation
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Protein Kinase Inhibitors / chemistry
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Protein Kinase Inhibitors / pharmacology*
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Receptor Protein-Tyrosine Kinases / antagonists & inhibitors*
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Receptor Protein-Tyrosine Kinases / chemistry
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Receptor Protein-Tyrosine Kinases / genetics
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Receptor Protein-Tyrosine Kinases / metabolism
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Receptor, Platelet-Derived Growth Factor beta / antagonists & inhibitors
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Receptor, Platelet-Derived Growth Factor beta / metabolism
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Signal Transduction / drug effects
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Time Factors
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Transfection
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Tubulin / metabolism
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Tubulin Modulators / chemistry
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Tubulin Modulators / pharmacology*
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Vascular Endothelial Growth Factor Receptor-2 / antagonists & inhibitors
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Vascular Endothelial Growth Factor Receptor-2 / metabolism
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Xenograft Model Antitumor Assays
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fms-Like Tyrosine Kinase 3 / antagonists & inhibitors
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fms-Like Tyrosine Kinase 3 / metabolism
Substances
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1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(2-cyano-4-hydroxyphenyl)urea
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Antineoplastic Agents
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Cell Cycle Proteins
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Phenylurea Compounds
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Protein Kinase Inhibitors
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Tubulin
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Tubulin Modulators
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EGFR protein, human
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ErbB Receptors
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FLT3 protein, human
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Receptor Protein-Tyrosine Kinases
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Receptor, Platelet-Derived Growth Factor beta
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Vascular Endothelial Growth Factor Receptor-2
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fms-Like Tyrosine Kinase 3