human GC tissues; paired noncancerous tissues; xenograft tumours; lung metastatic nodules
MKN28; AGS; SGC7901; MKN45; MGC803; BGC823; HEK-293T; GES-1
cell line-derived xenograft
Wnt/beta-catenin (inhibits); proliferation (inhibits); migration (inhibits); metastasis (inhibits); EMT (inhibits); ceRNA regulation (other)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; Actinomycin D / DRB Stability Assay; RT-qPCR; Microarray; FISH / smFISH; Clinical Sample Validation; RIP (RNA Immunoprecipitation); RNA Pull-Down; Luciferase Reporter Assay; Transfection; CCK8; EdU Staining; Colony Formation Assay; Transwell Assay; Wound Healing Assay; IF (Immunofluorescence); Western Blot; IHC (Immunohistochemistry); In Vivo Animal Model; Survival Analysis; Bioinformatics Analysis; Cohort Study
Low circFGD4 expression was correlated with poor tumour differentiation, lymphatic metastasis, and poor prognosis; circFGD4 may serve as a novel biomarker and therapeutic strategy for GC.
circFGD4 is a human FGD4-derived circRNA that is down-regulated in gastric cancer tissues and cell lines. It functions as a tumor suppressor by sponging miR-532-3p, increasing APC expression, and inactivating beta-catenin/Wnt/beta-catenin signaling, thereby inhibiting GC proliferation, migration, EMT, tumorigenesis and metastasis. Clinically, low circFGD4 expression is associated with poor differentiation, lymphatic metastasis and poor prognosis, supporting its potential as a GC biomarker and therapeutic target.
0.8961
Circular RNA circFGD4 suppresses gastric cancer progression via modulating miR-532-3p/APC/beta-catenin signalling pathway.
combined biological and clinical study