identified a vital effect exerted by miR-370 in regulating the glioblastoma development process, indicating that miR-370-3p acts as a neoplasm suppressor element; suppressing glioma cell growth; migration and invasion through HIF1A, HMGA2, and lncRNA NEAT1 targeting; and acting as a potential alternative to treat glioblastoma patients.22 This evidence concerns the gene NEAT1 and glioma.