{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Al-Dabet MM"],"funding":["Deutsche Forschungsgemeinschaft","NHLBI NIH HHS"],"pagination":["5062"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9420151"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["A major obstacle in diabetes is the metabolic or hyperglycemic memory, which lacks specific therapies. Here we show that glucose-mediated changes in gene expression largely persist in diabetic kidney disease (DKD) despite reversing hyperglycemia. The senescence-associated cyclin-dependent kinase inhibitor p21 (Cdkn1a) was the top hit among genes persistently induced by hyperglycemia and was associated with induction of the p53-p21 pathway. Persistent p21 induction was confirmed in various animal models, human samples and in vitro models. Tubular and urinary p21-levels were associated with DKD severity and remained elevated despite improved blood glucose levels in humans. Mechanistically, sustained tubular p21 expression in DKD is linked to demethylation of its promoter and reduced DNMT1 ex"],"journal":["Nature communications"],"pubmed_title":["Reversal of the renal hyperglycemic memory in diabetic kidney disease by targeting sustained tubular p21 expression."],"pmcid":["PMC9420151"],"funding_grant_id":["KO5736-/1-1","R15 HL127636"],"pubmed_authors":["Rana R","Gadi I","Al-Dabet MM","Bock F","Gupta D","Elwakiel A","Kohli S","Sulaj A","Kopf S","Scholz M","Dockendorff C","Fatima S","Griffin JH","Krishnan S","Keller M","Shahzad K","Manoharan J","Zimmermann S","Nawroth PP","Nazir S","Baber R","Mertens PR","Geffers R","Isermann B","Schwab C"],"additional_accession":[]},"is_claimable":false,"name":"Reversal of the renal hyperglycemic memory in diabetic kidney disease by targeting sustained tubular p21 expression.","description":"A major obstacle in diabetes is the metabolic or hyperglycemic memory, which lacks specific therapies. Here we show that glucose-mediated changes in gene expression largely persist in diabetic kidney disease (DKD) despite reversing hyperglycemia. The senescence-associated cyclin-dependent kinase inhibitor p21 (Cdkn1a) was the top hit among genes persistently induced by hyperglycemia and was associated with induction of the p53-p21 pathway. Persistent p21 induction was confirmed in various animal models, human samples and in vitro models. Tubular and urinary p21-levels were associated with DKD severity and remained elevated despite improved blood glucose levels in humans. Mechanistically, sustained tubular p21 expression in DKD is linked to demethylation of its promoter and reduced DNMT1 ex","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Aug","modification":"2025-04-18T19:06:40.496Z","creation":"2025-04-07T06:47:56.276Z"},"accession":"S-EPMC9420151","cross_references":{"pubmed":["36030260"],"doi":["10.1038/s41467-022-32477-9"]}}