Targeting β-catenin: PROTACs and precision degraders for Wnt-driven cancers

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Authors: Jonathan Trapani, Kailey P. Caroland, Yashi Ahmed, David J. Robbins, Vivian L. Weiss, Ethan Lee
Cited by: 5
References: 181

Abstract

The Wnt signaling pathway, a highly conserved molecular cascade, orchestrates critical biological processes including embryonic development, cell differentiation, and proliferation across diverse organisms. Despite the pivotal role that Wnt signaling plays in many diseases, most notably cancer, there are still no FDA-approved, efficacious drugs available that inhibit this pathway. Most Wnt inhibitors target upstream components (e.g., Wnt ligand production and receptors) rather than the most commonly mutated downstream proteins in the pathway. Consequently, there is considerable interest in developing drugs that target the downstream effector, β-catenin. This review examines the challenges in targeting β-catenin, current approaches, and insights into overcoming on-target toxicity associated with cadherin-bound β-catenin.

Fields of Study & Subjects

Protein Degradation and Inhibitors HER2/EGFR in Cancer Research Wnt/β-catenin signaling in development and cancer

Publication details

Journal / source
Frontiers in Oncology
Publisher
Frontiers Media SA
Volume
16
Pages
1777843–1777843
Publication date
2 February 2026
Language
EN