GC tissues; paracancerous tissues; subcutaneous tumor tissue; mouse serum
GES-1; HEK-293 T; HGC-27; AGS; MKN-45; MGC-803
cell line-derived xenograft
TGF-beta/SMAD (inhibits); proliferation (inhibits); migration (inhibits); invasion (inhibits); metastasis (inhibits); EMT (inhibits); apoptosis (promotes); inflammation (inhibits); ceRNA regulation (other)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; RT-qPCR; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; Luciferase Reporter Assay; Transfection; CCK8; Annexin V/PI Flow Cytometry; Transwell Assay; Wound Healing Assay; In Vivo Animal Model; ELISA; Western Blot; IF (Immunofluorescence); Cohort Study; Survival Analysis; Bioinformatics Analysis
Low circGAPVD1 expression correlates with larger tumor size and advanced TNM stage; high circGAPVD1 expression predicts better overall survival and suggests diagnostic, prognostic, and therapeutic potential in GC.
circGAPVD1 is a human GAPVD1-derived circRNA downregulated in gastric cancer tissues and cell lines. It suppresses GC progression by sponging miR-4424 to regulate STK4, encoding the tumor-suppressive GAPVD1-137aa protein, and inhibiting SMAD signaling, thereby reducing proliferation, migration, invasion, EMT, inflammation, and tumor growth while promoting apoptosis. Clinically, higher circGAPVD1 expression is associated with better overall survival and lower tumor size/TNM stage.
0.8557
circGAPVD1 inhibits the progression of gastric cancer through miR-4424/STK4 axis and encoding GAPVD1-137aa protein.
combined biological and clinical study