LSCC tissue; corresponding relative normal tissue; tumour tissues
Hep2; AMC-HN-8
cell line-derived xenograft
proliferation (promotes); migration (promotes); invasion (promotes); metastasis (promotes); EMT (promotes); apoptosis (inhibits); cell cycle (promotes); ceRNA regulation (promotes); other pathway/process (promotes)
RT-qPCR; Clinical Sample Validation; Transfection; CCK8; EdU Staining; Colony Formation Assay; Annexin V/PI Flow Cytometry; Cell Cycle Assay; Transwell Assay; IHC (Immunohistochemistry); IF (Immunofluorescence); Western Blot; In Vivo Animal Model; Survival Analysis; Cohort Study
High CDR1as levels were associated with high TNM stage, poor cellular differentiation, extensive lymph node metastasis, shorter survival time, poor clinical outcome, and potential diagnostic biomarker value in LSCC.
CDR1as is up-regulated in LSCC tissues and acts as an oncogenic circRNA. It promotes proliferation, cell-cycle progression, migration, invasion, EMT, and xenograft tumour growth by sponging miR-7 and increasing CCNE1 and PIK3CD expression. Clinically, high CDR1as expression is associated with advanced disease features and shorter survival, suggesting biomarker potential.
0.6745
CDR1as is overexpressed in laryngeal squamous cell carcinoma to promote the tumour's progression via miR-7 signals.
combined biological and clinical study