| Expression pattern: |
UP |
| Associated gene: |
mTOR signaling, p-mTOR, ATG5, LC3, Bcl-2, caspase-3 |
| Associated microRNA: |
- |
| Biological function: |
circCDK8 represses osteogenic differentiation of PDLSCs under hypoxia, induces autophagy and apoptosis, and circCDK8 silencing reverses the inhibitory effect of CoCl2 on osteogenic differentiation. |
| Molecular mechanism: |
circCDK8 induces ER stress/autophagy and apoptosis through mTOR signaling during hypoxia, thereby inhibiting osteogenic differentiation of PDLSCs. |
| Biological pathway or process: |
autophagy (promotes); apoptosis (promotes); other pathway/process (inhibits) |
| Detected method: |
Q
|
| Validation methods: |
RT-qPCR; Clinical Sample Validation; Transfection; CCK8; IF (Immunofluorescence); Annexin V/PI Flow Cytometry; Western Blot; Bioinformatics Analysis |
| Clinical significance: |
CircCDK8 could be a new therapeutic target of periodontitis. |
| Description: |
This study identifies hsa_circ_0003489/circCDK8 as an up-regulated circRNA in periodontitis tissues and in CoCl2-induced hypoxic PDLSCs. Functionally, circCDK8 promotes ER stress/autophagy and apoptosis through mTOR signaling, thereby repressing osteogenic differentiation of PDLSCs under hypoxia. Silencing circCDK8 reverses hypoxia-induced inhibition of osteogenesis, suggesting circCDK8 as a potential therapeutic target for periodontitis. |
| Confidence score: |
0.5732 |