BCa tissues; matched adjacent nontumor bladder tissues; bladder tissues; tumor tissues; lung tumor tissues
5637; T24; EJ; 253 J-BV; SV-HUC-1; HEK-293 T
cell line-derived xenograft
proliferation (inhibits); migration (inhibits); invasion (inhibits); metastasis (inhibits); EMT (inhibits); ceRNA regulation (other)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; Actinomycin D / DRB Stability Assay; RT-qPCR; RNA-seq; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RIP (RNA Immunoprecipitation); RNA Pull-Down; Luciferase Reporter Assay; Transfection; CCK8; Colony Formation Assay; Transwell Assay; Wound Healing Assay; In Vivo Animal Model; H&E Staining; IHC (Immunohistochemistry); Western Blot; Survival Analysis; ROC Analysis; Bioinformatics Analysis
Lower circSTK39 expression was associated with worse prognosis, advanced pathology stage, shorter overall survival, and potential diagnostic value; circSTK39 is proposed as a promising biomarker for diagnosis and prognosis of BCa patients.
circSTK39/hsa_circ_0001079 is a human STK39-derived circRNA that is downregulated in bladder cancer tissues and cell lines. It acts as a tumor-suppressive circRNA by sponging miR-135a-5p, increasing NR3C2 expression, and inhibiting EMT-associated proliferation, migration, invasion, tumor growth, and metastasis. Higher circSTK39 expression is associated with longer overall survival, and the study proposes circSTK39 as a diagnostic and prognostic biomarker for BCa.
0.8981
CircSTK39 suppresses the proliferation and invasion of bladder cancer by regulating the miR-135a-5p/NR3C2-mediated epithelial-mesenchymal transition signaling pathway.
combined biological and clinical study