Fig. 7From: Extracellular vesicles-derived microRNA-222 promotes immune escape via interacting with ATF3 to regulate AKT1 transcription in colorectal cancerSilencing of AKT1 antagonizes the effects of ATF3 knockdown on CRC cells. a, the activation of the AKT pathway in CRC cells treated with MSC-EVs alone or with si-ATF3/miR-222 inhibitor determined by western blot. Full-length blots are presented in Additional file 5 (Supplementary Figure S4); b, AKT1 expression in CRC cells; c, cell proliferation activity after co-transfection in cells assessed by EdU assay; d, tumor volume in xenograft models; e, assessment of tumorigenesis by tumor weight; f, percentage of CD3+ cells in tumor tissues detected by immunohistochemistry; g, expression of immune escape-related proteins in tumor tissues examined by western blot. Full-length blots are presented in Additional file 6 (Supplementary Figure S5). Unpaired t test was applied to analyze the differences between two experimental groups (panel f), while two-way ANOVA was utilized to analyze data among multiple groups, along with Tukey’s post hoc test (panel a, b, c, d, e and g)Back to article page