Gliomas are one of the most common and most aggressive types of central nervous system tumor. Angiogenesis is an important basis for the growth of solid tumors, including gliomas, which is regulated by microRNAs (miRNAs). However, the mechanism remains unclear. Recently, it was demonstrated that miR-24 was upregulated in gliomas, so the aim of the present study is to establish whether the dysregulation of miR-24 in glioma cells promotes microvascular proliferation of endothelial cells (ECs), and to investigate the potential mechanism. miR-24 was ovcrexpressed or downregulated in U251 glioma cell line cells using miR-24 mimics or inhibitors, respectively. Subsequently, the effects of conditional medium from miR-24 mimic- or inhibitor-transfected U251 cells on cell viability, migration and angiogenesis of human umbilical vein ECs (HUVECs) were examined. The expression levels of vascular endothelial growth factor (VEGF) mRNA, basic fibroblast growth factor (bFGF) mRNA, epidermal growth factor (EGF) mRNA, transforming growth factor (TGF)-beta mRNA, matrix metalloproteinase (MMP)-2 mRNA and MMP-9 mRNA, and the mRNA and protein levels of VEGF and TGF-beta in miR-24 mimic- or inhibitor-transfected U251 cells were obtained by reverse transcription-quantitative polymerase chain reaction and western blot analysis, respectively. The effects of conditional medium from miR-24 mimic- or inhibitor-transfected U251 cells on expression levels of VEGF mRNA, TGF-beta mRNA, MMP-2 mRNA and MMP-9 mRNA, and mRNA and protein expression levels of VEGF and TGF-beta, and intracellular AKT and beta-catenin signaling in HUVECs were also examined. The results indicated that the conditional medium from miR-24 mimic-transfected U251 cells exhibited significantly increased cell viability, cell migration and tube formation of HUVECs. By contrast, the conditional medium from miR-24 inhibitor-transfected U251 cells exhibited significantly decreased cell viability, cell migration and tube formation of HUVECs. Enforced expression of miR-24 in U251 cells may promote the cell viability and angiogenesis of HUVECs. The mRNA expression levels of VEGF, bFGF, EGF, TGF-beta, MMP-2 and MMP-9 in U251 cells were significantly increased by miR-24 mimics. Western blot detection confirmed the increased levels of VEGF and TGF-beta protein expression in U251 by miR-24 mimics, and the decrease of VEGF and TGF-beta protein expression levels in U251 by miR-24 inhibitors. The conditional medium from miR-24 mimic-transfected U251 cells increased the expression levels of the angiogenesis-associated factors, including VEGF, TGF-beta, MMP-2, and MMP-9. By contrast, reduced expression of miR-24 in U251 cells may downregulate the expression of those angiogenesis-associated factors. Thus, miR-24 in U251 cells may be important in the angiogenesis of HUVECs via VEGF and TGF-beta, and the intracellular signaling of AKT and beta-catenin may be involved in this process.