| Expression pattern: |
DN |
| Associated gene: |
NF-kappaB p65, SIRT1, Ago2 |
| Associated microRNA: |
miR-132 |
| Biological function: |
Inhibits inflammatory phenotypic switching of VSMCs, represses vascular inflammation, and alleviates injury-induced neointimal formation. |
| Molecular mechanism: |
circ-Sirt1 directly binds NF-kappaB p65 to sequester it in the cytoplasm and suppress NF-kappaB activity; additionally, it sponges miR-132/212 to relieve repression of SIRT1, increasing SIRT1-mediated deacetylation/inactivation of nuclear NF-kappaB p65. |
| Biological pathway or process: |
NF-kappaB (inhibits); inflammation (inhibits); ceRNA regulation (promotes) |
| Detected method: |
Q
H
|
| Validation methods: |
RT-qPCR; ISH (In Situ Hybridization); Clinical Sample Validation; Nuclear-Cytoplasmic Fractionation; RNase R Treatment; RIP (RNA Immunoprecipitation); RNA Pull-Down; Luciferase Reporter Assay; Transfection; Western Blot; IF (Immunofluorescence); In Vivo Animal Model; H&E Staining; ChIP / ChIP-seq; Co-IP |
| Clinical significance: |
circ-Sirt1 is decreased in atherosclerotic tissues and CAD plasma and may act as a biomarker for detection of patients with atherosclerosis. |
| Description: |
circ-Sirt1 is down-regulated in vascular injury/atherosclerosis-related settings and suppresses VSMC inflammatory phenotypic switching. Mechanistically, it directly binds NF-kappaB p65 to limit nuclear translocation and sponges miR-132/212 to increase SIRT1, thereby reducing p65 acetylation and NF-kappaB transcriptional activity. Its decreased level in patient tissues/plasma suggests biomarker potential in atherosclerosis/CAD. |
| Confidence score: |
0.802 |