UCB tissues; matched adjacent normal tissues; matched non-tumor tissues; patient-derived UCB organoids
T24; 5637; TCC-SUP; J82; RT4; UM-UC-3; SV-HUC-1
cell line-derived xenograft
proliferation (promotes); apoptosis (inhibits); oxidative phosphorylation (promotes); mitochondrial function (promotes); ubiquitination (inhibits); mRNA stability (promotes); other pathway/process (promotes)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; Actinomycin D / DRB Stability Assay; RT-qPCR; Microarray; FISH / smFISH; IF (Immunofluorescence); Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RIP (RNA Immunoprecipitation); RNA Pull-Down; Co-IP; Transfection; CCK8; Colony Formation Assay; Annexin V/PI Flow Cytometry; Flow Cytometry(Non-apoptosis/cycle); IHC (Immunohistochemistry); In Vivo Animal Model; Western Blot; Cohort Study; Survival Analysis; Bioinformatics Analysis
circRCP overexpression serves as an independent prognostic factor for poor survival in UCB patients; high co-expression of circRCP and LRPPRC predicts the poorest OS and may serve as a diagnostic/prognostic biomarker and therapeutic target.
circRCP is a human RAB11FIP1-derived circRNA that is frequently upregulated in UCB and predicts poor survival. It promotes UCB tumorigenesis by localizing predominantly to mitochondria and stabilizing the LRPPRC/SLIRP complex, thereby maintaining mitochondrial mRNA metabolism, oxidative phosphorylation, redox homeostasis and resistance to intrinsic apoptosis.
0.8981
Mitochondria-located circRCP regulates redox homeostasis via stabilizing LRPPRC/SLIRP complex to promote bladder urothelial carcinoma tumorigenesis.
combined biological and clinical study