gastric cancer tissues; colon cancer tissues; prostate cancer tissues; neuroblastoma tissues; adjacent normal tissues; ganglioneuroblastoma tissues; xenografts
MKN-45; AGS; HCT-116; PC-3; HEK293T; HeLa; LoVo; SH-SY5Y; SK-N-SH
cell line-derived xenograft
proliferation (promotes); migration (promotes); invasion (promotes); metastasis (promotes); angiogenesis (promotes); mRNA stability (promotes); other pathway/process (promotes)
Back-Splice Junction PCR / divergent primers PCR; RNase R Treatment; Sanger Sequencing; RT-qPCR; Northern Blot; FISH / smFISH; Nuclear-Cytoplasmic Fractionation; Clinical Sample Validation; RNA Pull-Down; Co-IP; RIP (RNA Immunoprecipitation); Luciferase Reporter Assay; Actinomycin D / DRB Stability Assay; Transfection; MTT; Colony Formation Assay; Transwell Assay; Wound Healing Assay; In Vivo Animal Model; H&E Staining; IHC (Immunohistochemistry); IF (Immunofluorescence); Western Blot; Survival Analysis; Bioinformatics Analysis; RNA-seq
CircAGO2 is highly expressed in gastric cancer tissues with metastasis, and high circAGO2 expression is associated with worse overall survival and poor outcome.
CircAGO2 is a human AGO2-derived intronic circRNA that is up-regulated in gastric cancer, colon cancer, prostate cancer, and neuroblastoma. It functions as an oncogenic circRNA by binding and activating HuR, thereby reducing AGO2/miRNA-mediated gene silencing of cancer progression-related target genes and promoting tumor growth, invasion, metastasis, and poor prognosis.
0.898
Circular RNA circAGO2 drives cancer progression through facilitating HuR-repressed functions of AGO2-miRNA complexes.
combined biological and clinical study