Deubiquitinase PSMD14 promotes tumorigenicity of glioblastoma by deubiquitinating and stabilizing β‐catenin

The deubiquitinating enzyme 26S proteasome non‐ATPase regulatory subunit 14 (PSMD14), a member of the JAB1/MPN/Mov34 metalloenzyme (JAMM) family, has been shown to function as an oncogene in various human cancers. However, the function of PSMD14 in glioma and the underlying mechanism remain unclear. In this study, our findings reveal a dramatic upregulation of PSMD14 in GBMs, which is associated with poor survival outcomes. Knocking down PSMD14 is associated with decreased proliferation and invasion of GBM cells in vitro and inhibited tumor growth in a xenograft mouse model. Mechanistically, PSMD14 directly interacts with β‐catenin, leading to a decrease in the K48‐linked ubiquitination of β‐catenin and subsequent β‐catenin stabilization. Increased β‐catenin expression significantly reverses the inhibitory effects of PSMD14 knockdown on the migration, invasion, and tumor growth of GBM cells. Moreover, we observed a significant correlation between PSMD14 and β‐catenin expression in human GBM samples. In summary, our results reveal that PSMD14 is a crucial deubiquitinase that is responsible for stabilizing the β‐catenin protein, highlighting its potential for use as a therapeutic target for GBM. PSMD14 is up‐regulated and promotes tumor growth in glioma. Mechanistically, PSMD14 promotes WNT/β‐catenin signaling through deubiquitinating and maintaining β‐catenin stability. In addition, PSMD14 promotes GBM cell proliferation, invasion, and tumor growth via the PSMD14/β‐catenin axis.