<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Jianye Yang</submitter><species>Rattus Norvegicus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0017820000</full_dataset_link><submitter_email>jianye_yang@hust.edu.cn</submitter_email><submitter_affiliation>Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>AQP9 Drives Myocardial Ferroptosis via TRIM25-Mediated GPX4 Ubiquitination and PI3K/AKT Suppression</name><description>This proteomics dataset investigates the role of aquaporin-9 (AQP9) in regulating ferroptosis during myocardial ischemia-reperfusion (I/R) injury. Quantitative proteomic analysis of H9c2 cardiomyocytes (shNC controls vs shAQP9 knockdowns) was performed on a Bruker timsTOF, and AQP9 immunoprecipitation-mass spectrometry (IP-MS) was acquired on a Thermo Q Exactive HF. The data reveal that AQP9 drives ferroptotic cell death by promoting GPX4 degradation via TRIM25-mediated ubiquitination while simultaneously inhibiting GPX4 synthesis through the PI3K/AKT pathway, thereby dismantling antioxidant defenses in ischemic cardiomyocytes.</description><dates><publication>Mon Jun 22 00:00:00 BST 2026</publication></dates><accession>PXD079978</accession><cross_references><TAXONOMY>10116</TAXONOMY></cross_references></HashMap>