Work

UBC9 silencing-mediated PPARα desumoylation induces inhibition of cell proliferation by ferroptosis in acute myeloid leukemia

Year: 2025

Type: article

Abstract: Introduction Inhibited acute myeloid leukemia (AML) proliferation is accompanied by downregulated peroxisome proliferator-activated receptor alpha (PPARα), which however can be stabilized via sumoylation. This study investigated how PPARα sumoylation impacts on AML cell growth. Material and methods Human AML HL-60 and tohoku hospital pediatrics-1 (THP-1) cells were treated with the PPARα inhibitor, GW6471 (10 µM), for 24 and 48 h. THP-1 cells were exposed to the PPARα agonist, pirinixic acid (10 µM), after the expression of the small ubiquitin-like modifier proteins (SUMO)-conjugating enzyme UBC9 was manipulated. The interaction between PPARα and SUMO1 was detected by immunoprecipitation assay. HL-60 and THP-1 cell viability, apoptosis and ferroptosis were measured via cell counting kit-8 assay, flow cytometry, BODIPY-C11 staining and/or colorimetric assay. UBC9, glutathione peroxidase 4 (GPX4), recombinant solute carrier family 7, member 11(SLC7A11) and PPARα expressions were analyzed by qRT-PCR or Western blot. Results GW6471 treatment for 24 and 48 h suppressed viability, promoted apoptosis and lipid peroxidation, increased the level of Fe2+, and decreased the expressions of GPX4, SLC7A11 and PPARα in HL-60/THP-1 cells. PPARα antibody induced enrichment of PPARα and SUMO1 in THP-1 cells, which was attenuated after UBC9 silencing. UBC9 silencing resulted in viability decrease, apoptosis and lipid peroxidation promotion, Fe2+ upregulation, and GPX4, SLC7A11 and PPARα downregulation in THP-1 cells, which were all counteracted by pirinixic acid. Conclusions UBC9 silencing-induced PPARα desumoylation induces suppression of AML cell growth by ferroptosis.

Source: Archives of Medical Science

DOI: 10.5114/aoms/204235