NPC biopsy tissue samples; nasopharyngeal epithelial tissue samples; subcutaneous tumor tissues; lung metastatic lesions
CNE2; HONE1; 5-8F; HNE2; C666-1; NP69
cell line-derived xenograft
Hippo/YAP (inhibits); proliferation (inhibits); migration (inhibits); invasion (inhibits); metastasis (inhibits); cell cycle (inhibits); ubiquitination (promotes); other pathway/process (inhibits)
Back-Splice Junction PCR / divergent primers PCR; Sanger Sequencing; RNase R Treatment; Actinomycin D / DRB Stability Assay; RT-qPCR; RNA-seq; FISH / smFISH; ISH (In Situ Hybridization); IHC (Immunohistochemistry); IF (Immunofluorescence); Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RIP (RNA Immunoprecipitation); RNA Pull-Down; Co-IP; Luciferase Reporter Assay; Transfection; MTT; Colony Formation Assay; Transwell Assay; Wound Healing Assay; In Vivo Animal Model; H&E Staining; Western Blot; Bioinformatics Analysis
circTP63-N may serve as a novel potential molecular marker and therapeutic target for clinical diagnosis and treatment of NPC.
circTP63-N is a novel TP63-derived circRNA that is significantly downregulated in nasopharyngeal carcinoma. It acts as a tumor suppressor by binding HSP90AB1, recruiting LATS1/2 and YAP1, promoting YAP1 phosphorylation and ubiquitination-dependent degradation, and suppressing YAP1/Hippo downstream oncogenic programs including INHBA, MMP3, and CCNE2. Restoration of circTP63-N inhibits NPC proliferation, invasion, migration, and metastasis in vitro and in vivo.
0.8869
circTP63-N suppresses the proliferation and metastasis of nasopharyngeal carcinoma via engaging with HSP90AB1 to modulate the YAP1/Hippo signaling pathway.
combined biological and clinical study