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NAT10-mediated ac4C-modification exacerbates ferroptosis by stabilizing HMOX1 in Deep vein thrombosis

ABSTRACT: In our study, we aimed to identify the pathways closely related to the pathogenesis of deep vein thrombosis. Through microarray analysis, we discovered the important pathway of ferroptosis.

ORGANISM(S): Homo sapiens

PROVIDER: GSE307102 | GEO | 2026/01/28

REPOSITORIES: GEO

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NAT10-mediated ac4C-modification exacerbates ferroptosis by stabilizing HMOX1 in Deep vein thrombosis

Project description:In our study, we aimed to identify the pathways and genes closely related to DVT. Through proteomic analysis, we found that the ferroptosis signaling pathway showed differential expression, and we also discovered that NAT10 (a key acetyltransferase modified by ac4C) was significantly overexpressed in DVT mice. Based on this discovery, we further investigated the downstream genes regulated by NAT10. We found that NAT10 enhances the stability of HMOX1 through ac4C modification, which results in iron overload and lipid peroxides, thereby forming a positive feedback loop that exacerbates DVT.

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