Aerobic glycolysis (the Warburg effect) promotes
tumor metastasis; hence, drugs targeting its regulators are being developed. c-Myc, a critical
transcription factor that regulates the Warburg effect, is involved in the
tumorigenesis of many
cancers, including
pancreatic cancer (PC). However, the upstream regulating mechanisms of c-Myc in PC are unclear. Herein, we reported that
E3 ubiquitin ligase RING-finger
protein 6 (RNF6) was upregulated in PC tissues, and an elevated RNF6 level was closely associated with
metastasis and poor prognosis in patients with PC. In functional experiments, RNF6 over-expression accelerated the metastatic ability of PC cells, whereas RNF6 knockdown impaired PC cell motility and invasiveness along with
metastasis in an orthotopic mouse model. Furthermore, we found that RNF6 promoted PC cell
metastasis by enhancing c-Myc-mediated aerobic glycolysis. Mechanistically, RNF6 increased the expression level of c-Myc by catalyzing the ubiquitination of Max-dimerization protein-1 (MAD1), a cellular antagonist of c-Myc. Lastly, RNF6 promoted the degradation of MAD1 via the
ubiquitin-
proteasome pathway, and this reduction in the MAD1 levels enabled c-Myc to promote the Warburg effect in PC. Our results demonstrate that RNF6 may be a novel
biomarker in PC
carcinogenesis, thereby indicating that targeting the RNF6/MAD1/c-Myc axis is a potential strategy for PC
therapy.