bladder cancer tissues; paired adjacent normal bladder tissues; adjacent normal bladder tissues; xenograft tumors
T24T; EJ; UMUC3; J82; 5637; SV-HUC-1
cell line-derived xenograft
proliferation (inhibits); cell cycle (inhibits); ceRNA regulation (other)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; RT-qPCR; RNA-seq; Northern Blot; FISH / smFISH; Clinical Sample Validation; RNA Pull-Down; Luciferase Reporter Assay; Transfection; CCK8; EdU Staining; Colony Formation Assay; Cell Cycle Assay; In Vivo Animal Model; IHC (Immunohistochemistry); Western Blot; Bioinformatics Analysis
circNR3C1 and miR-27a-3p were suggested as potential therapeutic targets for bladder cancer treatment; lower circNR3C1 expression was not correlated with clinical indicators including bladder cancer grade and pathological stage.
circNR3C1 is a human NR3C1-derived circRNA downregulated in bladder cancer tissues and cell lines. It acts as an anti-oncogenic cytoplasmic miRNA sponge for miR-27a-3p, reducing cyclin D1 protein expression, inducing G0/G1 arrest, and inhibiting bladder cancer cell proliferation and xenograft tumor growth. The study suggests circNR3C1 as a potential therapeutic target rather than a prognostic marker, since its lower expression was not correlated with grade or pathological stage.
0.866
CircNR3C1 inhibits proliferation of bladder cancer cells by sponging miR-27a-3p and downregulating cyclin D1 expression.
combined biological and clinical study