Function of the tumor suppressor RNF43 and gastrointestinal carcinogenesis
The canonical Wnt signaling pathway is essential in developmental processes and plays a crucial role in the regulation of epithelial stem cell self-renewal. Deregulation of this pathway is associated with carcinogenesis, particularly in the gastrointestinal tract. We identified a target gene of the Wnt signaling pathway, RNF43, which is selectively expressed in intestinal stem cells and is overexpressed in colorectal adenomas and a subset of colorectal cancers. Overexpression of RNF43 was shown to inhibit Wnt signaling in colon cancer cells by impairing Frizzled receptor turnover. Interestingly, we found an alternative mechanism of RNF43-mediated Wnt inhibition downstream of (mutated) β-catenin. Thus, RNF43 sequesters TCF4 to the nuclear membrane, dampening the transcription of important Wnt target genes (Loregger et al. Sci Signal. 2015). Mutations in RNF43 have been identified in several tumor types, suggesting an important role for RNF43 as a tumor suppressor gene. Indeed, depletion of RNF43 expression in colon and gastric cells increases their tumorigenic potential (Neumeyer et al. Carcinogenesis 2019). To further explore the function of RNF43 we have generated two mouse models expressing mutated Rnf43, which we are currently analyzing in different experimental settings.