Farnhammer Fiona, Colozza Gabriele, Kim Jihoon
Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter (VBC), Vienna, Austria.
Division of Oncology and Children's Research Center, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland.
Int J Stem Cells. 2023 Nov 30;16(4):376-384. doi: 10.15283/ijsc23070. Epub 2023 Aug 30.
The Wnt -catenin signaling pathway is a highly conserved mechanism that plays a critical role from embryonic development and adult stem cell homeostasis. However, dysregulation of the Wnt pathway has been implicated in various diseases, including cancer. Therefore, multiple layers of regulatory mechanisms tightly control the activation and suppression of the Wnt signal. The E3 ubiquitin ligases RNF43 and ZNRF3, which are known negative regulators of the Wnt pathway, are critical component of Wnt signaling regulation. These E3 ubiquitin ligases control Wnt signaling by targeting the Wnt receptor Frizzled to induce ubiquitination-mediated endo-lysosomal degradation, thus controlling the activation of the Wnt signaling pathway. We also discuss the regulatory mechanisms, interactors, and evolution of RNF43 and ZNRF3. This review article summarizes recent findings on RNF43 and ZNRF3 and their potential implications for the development of therapeutic strategies to target the Wnt signaling pathway in various diseases, including cancer.
Wnt-β-连环蛋白信号通路是一种高度保守的机制,在胚胎发育和成人干细胞稳态中起着关键作用。然而,Wnt通路的失调与包括癌症在内的各种疾病有关。因此,多层调节机制严格控制Wnt信号的激活和抑制。E3泛素连接酶RNF43和ZNRF3是已知的Wnt通路负调节因子,是Wnt信号调节的关键组成部分。这些E3泛素连接酶通过靶向Wnt受体卷曲蛋白来控制Wnt信号,以诱导泛素化介导的内体-溶酶体降解,从而控制Wnt信号通路的激活。我们还讨论了RNF43和ZNRF3的调节机制、相互作用因子和进化。这篇综述文章总结了关于RNF43和ZNRF3的最新发现,以及它们对开发针对包括癌症在内的各种疾病中Wnt信号通路的治疗策略的潜在意义。