Recently, increasing studies have suggested that
miRNAs play a significant role in the occurrence and development of
glioma. More researches are needed to explore the role of
miRNAs in
glioma, which will help to find new therapeutic targets. miR-212-5p has been reported to be involved in the progression in many
cancers. However, whether miR-212-5p has a regulative effect on
glioma remains un clear. In this study, we aimed to explore the effect of miR-212-5p on
glioma development and its mechanism. Here, we demonstrated that miR-212-5p was lowly expressed in
glioma cell. miR-212-5p suppressed the
glioma cell proliferation, inhibited the migratory and invasive capabilities and promoted apoptosis in
glioma cells. Besides, miR-212-5p also inhibited
tumor growth in vivo. We found small
ubiquitin-like modifier 2 (SUMO2) was the target of miR-212-5p, and miR-212-5p suppressed SUMO2 expression to regulate the proliferation, migration, and apoptosis of
glioma cells. These findings indicated that miR-212-5p may be a possible therapeutic target for the treatment for
glioma.