Identification of YL064 as a novel inhibitor of ATXN3 to suppress tumor growth and metastasis by promoting degradation of oncogenic substrates
TL;DR
YL064 is established as a promising ATXN3 inhibitor that targets the ubiquitin-proteasome pathway to exert anti-tumor effects, highlighting its potential as a novel therapeutic agent for ATXN3-driven cancers.
Abstract
ATXN3 has recently emerged as a pro-oncogenic deubiquitinating enzyme (DUB) involved in the progression of multiple cancers, including breast and prostate cancer. However, the therapeutic potential of targeting ATXN3 remains largely unexplored due to the lack of effective inhibitors. In this study, we performed an Ub-AMC-based high-throughput screening assay using full-length ATXN3 and identified YL064, a derivative of the natural product sinomenine isolated from Sinomenium acutum , as a novel ATXN3 inhibitor. Direct interaction between YL064 and ATXN3 was confirmed by thermal shift assay, cellular thermal shift assay, surface plasmon resonance, and molecular docking analysis. Functionally, YL064 suppressed cancer cell proliferation, induced cell-cycle arrest, and reduced metastatic potential. Mechanistically, YL064 inhibited ATXN3 deubiquitinating activity and promoted the ubiquitination and proteasomal degradation of ATXN3 substrates, including KLF4 and YAP. Furthermore, YL064 significantly inhibited tumor growth in an orthotopic breast cancer model in vivo. Collectively, our findings establish YL064 as a promising ATXN3 inhibitor that targets the ubiquitin-proteasome pathway to exert anti-tumor effects, highlighting its potential as a novel therapeutic agent for ATXN3-driven cancers.