| Expression pattern: |
UP |
| Associated gene: |
TRAM2 |
| Associated microRNA: |
miR-140-3p |
| Biological function: |
circ-STK39 promotes pancreatic cancer cell proliferation, migration, tumor growth, pulmonary metastasis, EMT and angiogenesis; downregulation of circ-STK39 suppresses these malignant phenotypes. |
| Molecular mechanism: |
circ-STK39 acts as a miR-140-3p sponge to enhance TRAM2 expression, thereby regulating TRAM2-mediated EMT in pancreatic cancer. |
| Biological pathway or process: |
proliferation (promotes); migration (promotes); metastasis (promotes); EMT (promotes); angiogenesis (promotes); ceRNA regulation (promotes) |
| Detected method: |
Q
H
S
|
| Validation methods: |
RT-qPCR; RNA-seq; FISH / smFISH; Clinical Sample Validation; Luciferase Reporter Assay; Transfection; CCK8; EdU Staining; Transwell Assay; In Vivo Animal Model; H&E Staining; IHC (Immunohistochemistry); Bioinformatics Analysis |
| Clinical significance: |
circ-STK39 was identified as a potential biomarker and potential therapeutic target for pancreatic cancer. |
| Description: |
circ-STK39/hsa_circ_0001079 is up-regulated in pancreatic cancer tissues and cell lines. The study shows that silencing circ-STK39 suppresses pancreatic cancer proliferation, migration, tumor growth, pulmonary metastasis and EMT by releasing miR-140-3p and reducing TRAM2-mediated EMT signaling, suggesting biomarker and therapeutic potential. |
| Confidence score: |
0.7486 |