CRC tissues; adjacent normal tissues; tumor tissues; liver tissues; peripheral blood
FHC; HT29; HCT116; LOVO; SW480; SW620
cell line-derived xenograft
proliferation (promotes); migration (promotes); invasion (promotes); metastasis (promotes); EMT (promotes); immune regulation (promotes); ceRNA regulation (promotes); apoptosis (other)
Bioinformatics Analysis; RT-qPCR; Clinical Sample Validation; Back-Splice Junction PCR / divergent primers PCR; Sanger Sequencing; RNase R Treatment; Actinomycin D / DRB Stability Assay; Transfection; CCK8; EdU Staining; Transwell Assay; Annexin V/PI Flow Cytometry; Western Blot; Flow Cytometry(Non-apoptosis/cycle); ELISA; Nuclear-Cytoplasmic Fractionation; RNA Pull-Down; Luciferase Reporter Assay; RIP (RNA Immunoprecipitation); In Vivo Animal Model; IHC (Immunohistochemistry); H&E Staining; Cohort Study; Survival Analysis
circEIF2S2 is associated with unfavorable clinical outcomes; high circEIF2S2 expression is associated with TNM stage, distant node metastasis, tumor differentiation, and poorer survival rates, suggesting potential prognostic and therapeutic value.
circEIF2S2 is a human colorectal cancer-associated circRNA that is significantly upregulated in CRC tissues and cell lines and whose high expression predicts poorer survival. It functions as an oncogenic and immunosuppressive circRNA by sponging miR-646 to increase UHMK1 expression, thereby promoting proliferation, migration, invasion, tumor growth, liver metastasis, EMT, PD-L1 expression, and suppression of CD8+ T cell responses. EIF4A3 acts upstream to promote circEIF2S2 biogenesis through interaction with EIF2S2 pre-mRNA.
0.8913
EIF4A3-induced circEIF2S2 facilitates colorectal cancer growth, metastasis, and immune suppression via the miR-646/UHMK1 Axis.
combined biological and clinical study