Fig. 6. LSECtin upregulates FN1/CHD4 expression and promotes GC progression via the circFBXL4/miR-146a-5p/STAT1 axis.
A LSECtin promoted the expression of miR-146a-5p in GC cells. B LSECtin inhibited the expression of hsa_circ_0077417 in GC cells. C Western blot experiments showed that LSECtin and miR-146a-5p coregulate STAT1 expression in GC cells. D Western blot experiments showed that LSECtin and circFBXL4 coregulate STAT1 expression in GC cells. E Western blot experiments showed that LSECtin upregulate FN1/CHD4 expression via the circFBXL4/miR-146a-5p axis. F Cell viability in different groups was detected by EdU assays, and the statistical analysis of EdU staining. G The migration of BGC-823 cells in different groups was detected by wound healing assays. H Transwell migration and invasion assays were performed to analyze the migration and invasion abilities of GC cells. I Adhesion between GC cells and frozen mouse lymph node sections in vitro was detected by H&E staining (left), The right panel shows the number of analysis of cells. J LSECtin expressed in lymph nodes of nude mice affected the expression of circFBXL4, miR-146a-5p and STAT1 in gastric cancer cells. K The expression of circFBXL4, miR-146a-5p and STAT1 in lymph nodes was correlated with statistical significance. Error bars indicate standard deviation (n = 3). Data, the means ± SD.
