{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["67"],"submitter":["Fan H"],"pubmed_abstract":["Reactive Oxygen Species (ROS) are widely accepted as a pernicious factor in the progression of intracranial aneurysm (IA), which is eminently related to cell apoptosis and extracellular matrix degradation, but the mechanism remains to be elucidated. Recent evidence has identified that enhancement of Cyclophilin D (CypD) under stress conditions plays a critical role in ROS output, thus accelerating vascular destruction. However, no study has confirmed whether cypD is a detrimental mediator of cell apoptosis and extracellular matrix degradation in the setting of IA development. Our data indicated that endogenous cypD mRNA was significantly upregulated in human IA lesions and mouse IA wall, accompanied by higher level of ROS, MMPs and cell apoptosis. CypD<sup>-/-</sup> remarkably reversed vas"],"journal":["Redox biology"],"pagination":["102887"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10514219"],"repository":["biostudies-literature"],"pubmed_title":["CypD induced ROS output promotes intracranial aneurysm formation and rupture by 8-OHdG/NLRP3/MMP9 pathway."],"pmcid":["PMC10514219"],"pubmed_authors":["Jin F","Liu Y","Li X","Su S","Fan H","Wen Z","Tian H","Zhang X","He X","Duan C"],"additional_accession":[]},"is_claimable":false,"name":"CypD induced ROS output promotes intracranial aneurysm formation and rupture by 8-OHdG/NLRP3/MMP9 pathway.","description":"Reactive Oxygen Species (ROS) are widely accepted as a pernicious factor in the progression of intracranial aneurysm (IA), which is eminently related to cell apoptosis and extracellular matrix degradation, but the mechanism remains to be elucidated. Recent evidence has identified that enhancement of Cyclophilin D (CypD) under stress conditions plays a critical role in ROS output, thus accelerating vascular destruction. However, no study has confirmed whether cypD is a detrimental mediator of cell apoptosis and extracellular matrix degradation in the setting of IA development. Our data indicated that endogenous cypD mRNA was significantly upregulated in human IA lesions and mouse IA wall, accompanied by higher level of ROS, MMPs and cell apoptosis. CypD<sup>-/-</sup> remarkably reversed vas","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Nov","modification":"2025-07-05T03:04:49.041Z","creation":"2025-04-06T15:58:49.581Z"},"accession":"S-EPMC10514219","cross_references":{"pubmed":["37717465"],"doi":["10.1016/j.redox.2023.102887"]}}