GC primary tumors; adjacent non-tumor tissue; tumor tissue
BGC-823; HGC-27; AGS; GES-1; 293 T
cell line-derived xenograft
Wnt/beta-catenin (promotes); proliferation (promotes); migration (promotes); invasion (promotes); metastasis (promotes); ceRNA regulation (promotes); immune regulation (promotes); other pathway/process (other)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; Actinomycin D / DRB Stability Assay; RT-qPCR; Microarray; Clinical Sample Validation; Luciferase Reporter Assay; Nuclear-Cytoplasmic Fractionation; Transfection; CCK8; EdU Staining; Colony Formation Assay; Transwell Assay; Wound Healing Assay; In Vivo Animal Model; H&E Staining; IHC (Immunohistochemistry); Western Blot; IF (Immunofluorescence); ChIP / ChIP-seq; Bioinformatics Analysis
High hsa_circ_0001479 expression is associated with tumor infiltration depth, lymph node metastasis, distant metastasis, TNM stage, and may serve as a biomarker for predicting immunotherapy efficacy in GC patients.
hsa_circ_0001479 is upregulated in gastric cancer and functions as an oncogenic circRNA that promotes GC cell proliferation, migration, invasion, and in vivo tumor growth. Mechanistically, it sponges miR-133a-5p to upregulate DEK and activate Wnt/beta-catenin/c-Myc signaling, while c-Myc further enhances hsa_circ_0001479 generation through ZNF131 promoter activation. The circRNA also contributes to immune escape by reducing CD8 + T cell infiltration and correlating with immune checkpoint molecules, suggesting potential immunotherapy biomarker value.
0.8686
Hsa_circ_0001479 accelerates tumorigenesis of gastric cancer and mediates immune escape.
combined biological and clinical study