plasma; peripheral blood samples; midbrain; SNpc; striatum
SH-SY5Y; HEK-293T; C8; BV2
other disease animal model
ceRNA regulation (other); autophagy (promotes); mitochondrial function (promotes); apoptosis (inhibits); proliferation (promotes); other pathway/process (promotes)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; RT-qPCR; RNA-seq; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RIP (RNA Immunoprecipitation); Luciferase Reporter Assay; Transfection; CCK8; Annexin V/PI Flow Cytometry; Flow Cytometry(Non-apoptosis/cycle); IF (Immunofluorescence); IHC (Immunohistochemistry); Western Blot; In Vivo Animal Model; ROC Analysis; Bioinformatics Analysis
circEPS15 is downregulated in PD patients, distinguishes PD patients from normal controls by ROC analysis, correlates negatively with H-Y stage and UPDRS motor score, and is proposed as a potential biomarker and therapeutic target for PD.
circEPS15 is downregulated in plasma of PD patients and in MPTP-induced PD mouse models, and lower levels correlate with worse PD motor severity. Functionally, circEPS15 overexpression protects dopaminergic neurons in vitro and in vivo by sponging MIR24-3p, increasing PINK1 expression, and boosting PINK1-PRKN-mediated mitophagy to maintain mitochondrial homeostasis. The study proposes circEPS15 as a potential biomarker and therapeutic target for Parkinson disease.
0.8792
CircEPS15, as a sponge of MIR24-3p ameliorates neuronal damage in Parkinson disease through boosting PINK1-PRKN-mediated mitophagy.
combined biological and clinical study