Combined transcriptomic and proteomic analyses reveal relevant myelin features in mice with ischemic stroke.
Ontology highlight
ABSTRACT: Ischemic stroke (IS), a leading cause of global disability and mortality, is characterized by white matter damage and demyelination. Despite advances, the molecular mechanisms driving post-IS myelin pathology remain poorly understood, limiting therapeutic development. This study investigates key myelin-related genes (MRGs) and their regulatory networks to identify novel therapeutic targets. A transient middle cerebral artery occlusion (MCAO) model was established in C57BL/6 mice, with brain tissues collected at four timepoints (Sham0D, MCAO0D, MCAO7D, MCAO14D). Transcriptomic and proteomic sequencing were performed, followed by soft clustering (Mfuzz), functional enrichment (GO/KEGG), and ROC analysis to identify key MRGs. Competing endogenous RNA (ceRNA) networks were constructed, and dru
SUBMITTER: Qian Q
PROVIDER: S-EPMC11909235 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA