Hepatocellular carcinoma (HCC) is a major threat to human health worldwide. Its suboptimal responses to current therapies are largely attributable to the immunosuppressive tumor microenvironment (TME) that dampens the efficiency of available treatments. Although metabolic reprogramming is regarded as a hallmark of HCC, the exact role of peroxisomal metabolism in immune evasion is poorly understood. By integrating bioinformatic analysis of TCGA-LIHC datasets and peroxisomal gene profiling, glyceronephosphate O-acyltransferase (GNPAT) was identified as a regulator of HCC pathogenesis. GNPAT was highly expressed in malignant tissues and positively associated with poor clinical outcomes and immunosuppressive cellular infiltration types. Functional experiments showed that GNPAT facilitated the proliferation, migration, and resistance to apoptosis of HCC cells in an autocrine manner via enhancing plasmalogen synthesis and downstream PPAR pathway activation. Interestingly, overexpression of GNPAT in HCC cells polarized macrophages to the M2-like phenotype and reinforced immunosuppressive TME through the plasmalogen-PPAR axis. An unrecognized mode of immunometabolic crosstalk mediated by peroxisomal metabolism in HCC was thereby revealed, providing a preclinical rationale and mechanistic basis for future exploration of GNPAT inhibition as a potential therapeutic strategy to antagonize immunosuppression and enhance antitumor immunity.
Hu et al. (Tue,) studied this question.