{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["31(11)"],"submitter":["Hong J"],"pubmed_abstract":["Hyperglycaemia-induced ferroptosis is a significant contributor to kidney dysfunction in diabetic nephropathy (DN) patients. In addition, targeting ferroptosis has clinical implications for the treatment of DN. However, effective therapeutic targets for ferroptosis have not been identified. In this study, we aimed to explore the precise role of protein arginine methyltransferase 6 (PRMT6) in regulating ferroptosis in DN. In the present study, we utilized a mouse DN model consisting of both wild-type and PRMT6-knockout (PRMT6<sup>-/-</sup>) mice. Transcriptomic and lipidomic analyses, along with various molecular biological methodologies, were used to determine the potential mechanism by which PRMT6 regulates ferroptosis in DN. Our results indicate that PRMT6 downregulation participates in "],"journal":["Cell death and differentiation"],"pagination":["1561-1575"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11519485"],"repository":["biostudies-literature"],"pubmed_title":["The PRMT6/STAT1/ACSL1 axis promotes ferroptosis in diabetic nephropathy."],"pmcid":["PMC11519485"],"pubmed_authors":["Li X","Zhu M","Yu L","Zhang J","Hong J","Hao Y","Xu H","Meng Z"],"additional_accession":[]},"is_claimable":false,"name":"The PRMT6/STAT1/ACSL1 axis promotes ferroptosis in diabetic nephropathy.","description":"Hyperglycaemia-induced ferroptosis is a significant contributor to kidney dysfunction in diabetic nephropathy (DN) patients. In addition, targeting ferroptosis has clinical implications for the treatment of DN. However, effective therapeutic targets for ferroptosis have not been identified. In this study, we aimed to explore the precise role of protein arginine methyltransferase 6 (PRMT6) in regulating ferroptosis in DN. In the present study, we utilized a mouse DN model consisting of both wild-type and PRMT6-knockout (PRMT6<sup>-/-</sup>) mice. Transcriptomic and lipidomic analyses, along with various molecular biological methodologies, were used to determine the potential mechanism by which PRMT6 regulates ferroptosis in DN. Our results indicate that PRMT6 downregulation participates in ","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Nov","modification":"2026-06-05T07:32:08.137Z","creation":"2026-05-14T03:12:51.71Z"},"accession":"S-EPMC11519485","cross_references":{"pubmed":["39134684"],"doi":["10.1038/s41418-024-01357-8"]}}