Development of small molecules targeting the Wnt pathway for the treatment of colon cancer: a high-throughput screening approach
Author(s) -
Wei Chen,
Minyong Chen,
Larry S. Barak
Publication year - 2010
Publication title -
ajp gastrointestinal and liver physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.644
H-Index - 169
eISSN - 1522-1547
pISSN - 0193-1857
DOI - 10.1152/ajpgi.00005.2010
Subject(s) - wnt signaling pathway , drug discovery , small molecule , colorectal cancer , high throughput screening , computational biology , drug , niclosamide , cancer , drug development , biology , signal transduction , cancer research , bioinformatics , pharmacology , microbiology and biotechnology , biochemistry , genetics , ecology
Wnt proteins play major roles in development and differentiation, and abnormalities in their regulation are believed to contribute to the formation of many cancers, including colorectal malignancies. As a result, there has been an interest in identifying small molecule inhibitors of Wnt signaling as tool compounds for research or as precursors to new generations of anticancer drugs. Advancements in robotic technology along with reductions in the costs of equipment, chemical libraries, and information handling have made high-throughput drug discovery programs possible in an academic setting. In this minireview we discuss the most plausible protein targets for inhibiting Wnt signaling in colon cancer therapy, list small molecule Wnt inhibitors that have been identified through recent drug discovery efforts, and provide our laboratory's strategy for identifying novel Wnt signaling antagonists using high-throughput screening. In particular, we summarize the results of a screen of over 1,200 drug and druglike compounds we recently completed in which niclosamide was identified as a Wnt pathway antagonist.
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