| Literature DB >> 28043913 |
Yonghe Li1, Patsy G Oliver2, Wenyan Lu3, Vibha Pathak3, Sivaram Sridharan2, Corinne E Augelli-Szafran3, Donald J Buchsbaum2, Mark J Suto3.
Abstract
Activation of Wnt/β-catenin signaling is associated with pancreatic and colorectal cancer, among others. To-date, there are no FDA-approved small molecule Wnt/β-catenin inhibitors and many past efforts resulted in compounds with undesirable off-target effects. We recently identified a series of benzimidazole analogs as potent inhibitors of Wnt/β-catenin signaling. Here, we show that the lead compound SRI36160 displayed selective Wnt inhibition and potent antiproliferative activity in pancreatic and colorectal cancer cells. Moreover, SRI36160 had no effect on STAT3 and mTORC1 signaling in pancreatic and colorectal cancer cells, and was not effective in inhibiting proliferation of non-cancerous cells. Our findings suggest that this series of benzimidazole analogs presents a novel approach for the treatment of Wnt-dependent cancers such as colorectal and pancreatic cancer.Entities:
Keywords: Benzimidazole; Drug discovery; Niclosamide; Targeted therapy; Wnt signaling
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Year: 2016 PMID: 28043913 PMCID: PMC5544029 DOI: 10.1016/j.canlet.2016.12.030
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679