Li Shanshan, Niu Jiahui, Smits Ron
Department of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, the Netherlands.
Department of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, the Netherlands..
Biochim Biophys Acta Rev Cancer. 2024 Nov;1879(6):189217. doi: 10.1016/j.bbcan.2024.189217. Epub 2024 Nov 17.
RNF43 and ZNRF3 are recognized as important regulators of Wnt/β-catenin signaling by maintaining Wnt-receptors at minimal essential levels. In various cancer types, particularly gastrointestinal tumors, mutations in these genes lead to abnormal Wnt-dependent activation of β-catenin signaling. However, recent findings implicate RNF43/ZNRF3 also in the regulation of other tumor-related proteins, including EGFR, BRAF, and the BMP-signaling pathway, which may have important implications for tumor biology. Additionally, we describe in detail how phosphorylation and ubiquitination may finetune RNF43 and ZNRF3 activity. We also address the variety of mutations observed in cancers and the mechanism through which they support tumor growth, and challenge the prevailing view that specific missense mutations in the R-spondin and RING domains may possess dominant-negative activity in contributing to tumor formation.
RNF43和ZNRF3被认为是Wnt/β-连环蛋白信号通路的重要调节因子,它们通过将Wnt受体维持在最低必需水平来发挥作用。在各种癌症类型中,尤其是胃肠道肿瘤,这些基因的突变会导致β-连环蛋白信号通路的异常Wnt依赖性激活。然而,最近的研究发现RNF43/ZNRF3也参与调节其他肿瘤相关蛋白,包括表皮生长因子受体(EGFR)、BRAF和骨形态发生蛋白(BMP)信号通路,这可能对肿瘤生物学具有重要意义。此外,我们详细描述了磷酸化和泛素化如何微调RNF43和ZNRF3的活性。我们还探讨了在癌症中观察到的各种突变以及它们支持肿瘤生长的机制,并对R-spondin和RING结构域中的特定错义突变可能在促进肿瘤形成中具有显性负性活性这一普遍观点提出了质疑。