Abstract
Inherited and somatic mutations in the APC gene, a human tumor-suppressor, occur in a large percentage of colon cancers, leading to elevated levels of nuclear beta-Catenin, and to activation of TCF/beta-Catenin-responsive genes including cyclin D1 and c-myc. To identify small molecule antagonists of this pathway, we screened transformed colorectal cells with a secondary structure-templated chemical library, in search of compounds that attenuated a TCF/beta-Catenin-responsive reporter gene. From this library we selected ICG-001 (IC50=3 microM) as a lead compound. Design and synthesis of the chemical library and some preliminary biological evaluation is described.
MeSH terms
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Bridged Bicyclo Compounds, Heterocyclic / chemical synthesis
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Bridged Bicyclo Compounds, Heterocyclic / chemistry
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Bridged Bicyclo Compounds, Heterocyclic / pharmacology*
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Cell Line
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Cells, Cultured
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Drug Design
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Drug Screening Assays, Antitumor
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Humans
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Molecular Structure
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Pyrimidinones / chemical synthesis
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Pyrimidinones / chemistry
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Pyrimidinones / pharmacology*
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Structure-Activity Relationship
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TCF Transcription Factors / antagonists & inhibitors*
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TCF Transcription Factors / genetics
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TCF Transcription Factors / metabolism*
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Transcription, Genetic / drug effects
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beta Catenin / antagonists & inhibitors*
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beta Catenin / genetics
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beta Catenin / metabolism*
Substances
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Bridged Bicyclo Compounds, Heterocyclic
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ICG 001
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Pyrimidinones
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TCF Transcription Factors
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beta Catenin