HMGCL-induced β-Hydroxybutyrate Production Attenuates Hepatocellular Carcinoma via DPP4-mediated Ferroptosis Susceptibility

Abstract

Abstract Background: Metabolic disorder is an essential characteristic of tumor development. Ketogenesis as a heterogeneous factor in multiple cancer, but the effect of ketogenesis on hepatocellular carcinoma (HCC) is elusive. Methods: We aimed to explain a role of ketogenesis related hydroxymethylglutaryl-CoA lyase (HMGCL) on HCC suppression. Expression pattern of HMGCL in HCC specimens was evaluated by immunohistochemistry (IHC). HMGCL was depleted or overexpressed in HCC cells to investigate the functions of HMGCL in vitro and in vivo. The antitumor function of HMGCL was studied in subcutaneous xenograft and Trp53Δhep/Δhep; c-Myc-driven HCC mouse models. The mechanism of HMGCL mediated tumor suppression was studied by IHC, western blot (WB) and Cut & Tag. Results: HMGCL depletion promoted HCC proliferation and metastasis, whereas its overexpression reversed this trend. As HMGCL catalyzes β-hydroxybutyric acid (β-OHB) production, we discovered that HMGCL increased acetylation at histone H3K9, which further promoted the transcription of Dipeptidyl peptidase-4 (DPP4), a key protein maintains intracellular lipid peroxidation and iron accumulation, leading to HCC cells vulnerability to erastin- and sorafenib-induced ferroptosis. Conclusions: Our study identified a critical role of HMGCL on HCC suppression, of which HMGCL regulated H3K9 acetylation through β-OHB and modulating the expression of DPP4 in a dose-dependent manner, which led to ferroptosis in HCC cells.