Tumor tissues; adjacent normal nasopharyngeal tissues; NPC tissues; tumor xenografts; lungs; inguinal lymph nodes
NP69; HK-1; C666-1; HEK293T; HEK293
cell line-derived xenograft
proliferation (promotes); migration (promotes); invasion (promotes); metastasis (promotes); EMT (promotes); ceRNA regulation (promotes); ubiquitination (promotes)
RNase R Treatment; RT-qPCR; Northern Blot; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RIP (RNA Immunoprecipitation); RNA Pull-Down; Luciferase Reporter Assay; Transfection; EdU Staining; Colony Formation Assay; Transwell Assay; IF (Immunofluorescence); Western Blot; Co-IP; In Vivo Animal Model; H&E Staining; Cohort Study; Survival Analysis; Bioinformatics Analysis
High circMAN1A2 expression is associated with severer lymph node metastasis and tumor staging and predicts shorter OS, DFS, and DMFS in NPC patients; it may be a potential therapeutic target and may provide a potential novel target for future diagnosis and prognosis.
circMAN1A2 is up-regulated in NPC tissues and cells and its high expression is associated with shorter OS, DFS, and DMFS. Functionally, circMAN1A2 promotes NPC proliferation, migration, invasion, EMT, tumor growth, and metastasis. Mechanistically, cytoplasmic circMAN1A2 sponges miR-135a-3p to increase UBR5 expression, leading to UBR5-mediated ubiquitination of ATMIN.
0.8637
CircMAN1A2 contributes to nasopharyngeal carcinoma progression via enhancing the ubiquitination of ATMIN through miR-135a-3p/UBR5 axis.
combined biological and clinical study