Browse views: by Year, by Function, by GLF, by Subfunction, by Conference, by Journal

Inhibition of wnt/β-catenin signaling in neuroendocrine tumors in vitro: Antitumoral effects

Jin, Xi-Feng and Spöttl, Gerald and Maurer, Julian and Nölting, Svenja and Auernhammer, Christoph J. (2020) Inhibition of wnt/β-catenin signaling in neuroendocrine tumors in vitro: Antitumoral effects. Cancers, 12 (2). p. 345. ISSN 20726694

Abstract

Background and aims: Inhibition of Wnt/β-catenin signaling by specific inhibitors is currently being investigated as an antitumoral strategy for various cancers. The role of Wnt/β-catenin signaling in neuroendocrine tumors still needs to be further investigated. Methods: This study investigated the antitumor activity of the porcupine (PORCN) inhibitor WNT974 and the β-catenin inhibitor PRI-724 in human neuroendocrine tumor (NET) cell lines BON1, QGP-1, and NCI-H727 in vitro. NET cells were treated with WNT974, PRI-724, or small interfering ribonucleic acids against β-catenin, and subsequent analyses included cell viability assays, flow cy-tometric cell cycle analysis, caspase3/7 assays and Western blot analysis. Results: Treatment of NET cells with WNT974 significantly reduced NET cell viability in a dose-and time-dependent manner by inducing NET cell cycle arrest at the G1 and G2/M phases without inducing apoptosis. WNT974 primarily blocked Wnt/β-catenin signaling by the dose-and time-dependent downregulation of low-density lipoprotein receptor-related protein 6 (LRP6) phosphorylation and non-phosphorylated β-catenin and total β-catenin, as well as the genes targeting the latter (c-Myc and cyclinD1). Furthermore, the WNT974-induced reduction of NET cell viability occurred through the inhibition of GSK-3-dependent or independent signaling (including pAKT/mTOR, pEGFR and pIGFR signaling). Similarly, treatment of NET cells with the β-catenin inhibitor PRI-724 caused significant growth inhibition, while the knockdown of β-catenin expression by siRNA reduced NET tumor cell viability of BON1 cells but not of NCI-H727 cells. Conclusions: The PORCN inhibitor WNT974 possesses antitumor properties in NET cell lines by inhibiting Wnt and related signaling. In addition, the β-catenin inhibitor PRI-724 possesses antitumor properties in NET cell lines. Future studies are needed to determine the role of Wnt/β-catenin signaling in NET as a potential therapeutic target.

Item Type: Article
Keywords: Neuroendocrine tumor Porcupine inhibitor Wnt/β-catenin signaling β-catenin inhibitor β-catenin siRNA
Date Deposited: 11 Mar 2020 00:45
Last Modified: 11 Mar 2020 00:45
URI: https://oak.novartis.com/id/eprint/40747

Search

Email Alerts

Register with OAK to receive email alerts for saved searches.