miR‐1254 inhibits progression of glioma in vivo and in vitro by targeting CSF‐1

The role of miRNAs (microRNAs) has been implicated in glioma initiation and progression, although the inherent biochemical mechanisms still remain to be unravelled. This study strived to evaluate the association between CSF‐1 and miR‐1254 and their effect on advancement of glioma cells. The levels of miR‐1254 in glioma cells and tissues were determined by real‐time RT‐PCR. Proliferation, apoptosis and cell cycle arrest, invasion and migration, were assessed by CCK‐8 assay, colony formation assay, flow cytometry, transwell assay and wound‐healing assay, respectively. The targeted relationship between miR‐1254 and CSF‐1 was confirmed by dual‐luciferase reporter assay. The effects of CSF‐1 on cellular functions were also assessed. The in vivo effect of miR‐1254 on the formation of a tumour was explored by using the mouse xenograft model. We found in both glioma tissues and glioma cells, the down‐regulated expressions of miR‐1254 while that of CSF‐1 was abnormally higher than normal level. The target relationship between CSF‐1 and miR‐1254 was validated by dual‐luciferase reporter assay. The CSF‐1 down‐regulation or miR‐1254 overexpression impeded the invasion, proliferation and migratory ability of U251 and U87 glioma cells, concurrently occluded the cell cycle and induced cell apoptosis. Moreover, in vivo tumour development was repressed due to miR‐1254 overexpression. Thus, CSF‐1 is targeted directly by miR‐1254, and the miR‐1254/CSF‐1 axis may be a potential diagnostic target for malignant glioma.