PRMT5 acts as a tumor suppressor by inhibiting Wnt/β-catenin signaling in murine gastric tumorigenesis.

Previous studies have demonstrated the oncogenic role of protein arginine methyltransferase 5 (PRMT5) in gastric cancer cell lines. The function of PRMT5 in gastric tumorigenesis, however, is still unexplored. Here, we showed that deletion in mouse gastric epithelium resulted in spontaneous tumorigenesis in gastric antrum. All -deficient mice displayed intestinal-type gastric cancer within 4 months of age. Of note, 20% (2/10) of mutants finally developed into invasive gastric cancer by 8 months of age. Gastric cancer caused by PRMT5 loss exhibited the increase in Lgr5 stem cells, which are proposed to contribute to both the gastric tumorigenesis and progression in mouse models. Consistent with the notion that Lgr5 is the target of Wnt/β-catenin signaling, whose activation is the most predominant driver for gastric tumorigenesis, mutant gastric cancer showed the activation of Wnt/β-Catenin signaling. Furthermore, in human gastric cancer samples, deletion and downregulation were frequently observed and associated with the poor prognosis. We propose that as opposed to the tumor-promoting role of PRMT5 well-established in the progression of various cancer types, PRMT5 functions as a tumor suppressor , at least during gastric tumor formation.