Pharmacological inhibition of the Wnt acyltransferase PORCN prevents growth of WNT-driven mammary cancer

KD Proffitt, B Madan, Z Ke, V Pendharkar, L Ding… - Cancer research, 2013 - AACR
KD Proffitt, B Madan, Z Ke, V Pendharkar, L Ding, MA Lee, RN Hannoush, DM Virshup
Cancer research, 2013AACR
Porcupine (PORCN) is a membrane bound O-acyltransferase that is required for Wnt
palmitoylation, secretion, and biologic activity. All evaluable human Wnts require PORCN for
their activity, suggesting that inhibition of PORCN could be an effective treatment for cancers
dependent on excess Wnt activity. In this study, we evaluated the PORCN inhibitor Wnt-C59
(C59), to determine its activity and toxicity in cultured cells and mice. C59 inhibits PORCN
activity in vitro at nanomolar concentrations, as assessed by inhibition of Wnt palmitoylation …
Abstract
Porcupine (PORCN) is a membrane bound O-acyltransferase that is required for Wnt palmitoylation, secretion, and biologic activity. All evaluable human Wnts require PORCN for their activity, suggesting that inhibition of PORCN could be an effective treatment for cancers dependent on excess Wnt activity. In this study, we evaluated the PORCN inhibitor Wnt-C59 (C59), to determine its activity and toxicity in cultured cells and mice. C59 inhibits PORCN activity in vitro at nanomolar concentrations, as assessed by inhibition of Wnt palmitoylation, Wnt interaction with the carrier protein Wntless/WLS, Wnt secretion, and Wnt activation of β-catenin reporter activity. In mice, C59 displayed good bioavailability, as once daily oral administration was sufficient to maintain blood concentrations well above the IC50. C59 blocked progression of mammary tumors in MMTV-WNT1 transgenic mice while downregulating Wnt/β-catenin target genes. Surprisingly, mice exhibit no apparent toxicity, such that at a therapeutically effective dose there were no pathologic changes in the gut or other tissues. These results offer preclinical proof-of-concept that inhibiting mammalian Wnts can be achieved by targeting PORCN with small-molecule inhibitors such as C59, and that this is a safe and feasible strategy in vivo. Cancer Res; 73(2); 502–7. ©2012 AACR.
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