Mechanistic insights into ENO2-driven glycolysis and tumor progression in hepatocellular carcinoma
Yan Liu, Xiao-Ran Zhang, Li Dai, Hai-Liang Li, Xiang-Ren Jin, Hong-Bin Qi, Ke Tang, Qiang LiBackground and Aims
Neuron-specific enolase 2 (ENO2) has been implicated in tumor metabolism, but its biological role in hepatocellular carcinoma remains incompletely defined. This study aimed to investigate the expression, prognostic relevance, and functional role of ENO2 in HCC.
Methods
Public transcriptomic datasets, RNA sequencing, WGCNA, survival analyses, and pathway enrichment analyses were integrated to identify HCC-associated genes. ENO2 expression was validated in HCC cell lines and paired clinical tissues.Gain- and loss-of-function, catalytic-rescue, glycolytic-inhibition, and pyruvate-rescue experiments were performed to evaluate glycolytic activity, proliferation, colony formation, migration, invasion, and tumor growth.
Results
ENO2 was upregulated in HCC and was associated with advanced tumor stage and unfavorable survival outcomes in public datasets. ENO2 overexpression increased glycolytic activity and malignant phenotypes, whereas ENO2 depletion produced opposite effects. In ENO2-depleted cells, re-expression of shRNA-resistant ENO2 wild type restored the impaired glycolytic and malignant phenotypes, whereas the catalytic-deficient ENO2 mutant failed to restore them. Moreover, 2-deoxy-D-glucose attenuated ENO2 overexpression-associated phenotypes, while pyruvate partially rescued phenotypes associated with ENO2 depletion. ENO2 expression was also associated with altered PI3K and AKT phosphorylation.
Conclusions
ENO2 may contribute to HCC progression by enhancing glycolytic metabolism and malignant phenotypes, partly in association with PI3K/AKT signaling. ENO2 is a candidate metabolic and prognostic biomarker that requires validation in larger independent clinical cohorts and warrants further investigation as a therapeutic candidate.