<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Liang Jin</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0017595000</full_dataset_link><submitter_email>6238564@qq.com</submitter_email><submitter_affiliation>China Pharmaceutical University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>CBX4 stabilizes NEUROD1 through SUMO-ubiquitin crosstalk to delay β-cell senescence</name><description>CBX4 expression is progressively lost in aged and diabetic pancreatic β-cells, correlating with cellular senescence. Mechanistically, CBX4 stabilizes NEUROD1 by promoting its SUMOylation at lysine 38, which antagonizes NEDD4-mediated ubiquitination. Stabilized NEUROD1 enhances insulin transcription and activates CaMKII signaling by suppressing Camk2n1 expression. This cascade preserves mitochondrial function and calcium homeostasis in β-cells. Thus, the STAT5A-CBX4-NEUROD1 axis represents a key protective pathway against β-cell aging and a potential therapeutic target for T2DM.</description><dates><publication>Thu Jun 04 00:00:00 BST 2026</publication></dates><accession>PXD079253</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>