Journal
CELLULAR SIGNALLING
Volume 26, Issue 6, Pages 1303-1309Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2014.02.018
Keywords
LRP6; Wnt signaling; mTORCI signaling; Rottlerin; Cancer; Drug discovery
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Funding
- National Institutes of Health [R01CAl24531, R21CA182056]
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Activation of Wnt/beta-catenin signaling can result in up-regulation of mTORC1 signaling in cancer cells. The low density lipoprotein receptor-related protein-6 (LRP6) is an essential Wnt co-receptor for Wnt/S-catenin signaling. We found that rottlerin, a natural plant polyphenol, suppressed LRP6 expression and phosphotylation, and inhibited Wnt43-catenin signaling in HEK293 cells. Furthermore, the inhibitory effects of rottlerin on LRP6 expression/phosphorylation and Wnt/beta-catenin signaling were confirmed in human prostate cancer PC-3 and DU145 cells and breast cancer MDA-MB-231 and T-47D cells. Mechanistically, rottlerin promoted LRP6 degradation, but had no effects on LRP6 transcriptional activity. In addition, rottlerin-mediated LRP6 downregulation was unrelated to activation of 5'-AMP-activated protein kinase (AMPK). Importantly, we also found that rottlerin inhibited mTORC1 signaling in prostate and breast cancer cells. Finally, we demonstrated that rottlerin was able to suppress the expression of cyclin D1 and survivin, two targets of both Wnt/S-catenin and mTORC1 signaling, in prostate and breast cancer cells, and displayed remarkable anticancer activity with IC50 values between 0.7 and 1.7 mu M for prostate cancer PC-3 and DU145 cells and breast cancer MDA-MB-231 and T-47D cells. The IC50 values are comparable to those shown to suppress the activities of Wnt/S-catenin and mTORC1 signaling in prostate and breast cancer cells. Our data indicate that rottlerin is a novel LRP6 inhibitor and suppresses both Wnt/S-catenin and mTORC1 signaling in prostate and breast cancer cells, and that LRP6 represents a potential therapeutic target for cancers. (c) 2014 Elsevier B.V. All rights reserved.
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