Osteosarcoma accounts for about 0.2% in human malignant solid
tumors. The mortality and metastatic rates of
osteosarcoma remain relatively high.
MicroRNA (
miRNA) is a kind of non-coding small-molecular
RNA discovered in recent years. Various studies have identified the involvement of
miRNA in the occurrence and development of
tumor as an oncogene or tumor-suppressor gene. This study aims to investigate the effect of hsa-miR-889-3p on the progression of
osteosarcoma and its underlying mechanism. Through the bioinformatics methods, we first found that hsa-miR-889-3p was upregulated in
osteosarcoma, and it was a prognostic risk factor for
osteosarcoma. Additionally, the gene set enrichment analysis (GSEA) revealed that hsa-miR-889-3p mainly affected cell cycle progression and proliferation of
osteosarcoma. To verify the bioinformatics results, regulatory effects of hsa-miR-889-3p on
osteosarcoma both in vitro and in vivo experiments were investigated. It is found that hsa-miR-889-3p could promote the proliferation of
osteosarcoma cells though regulating cell cycle progression.
Tumor size and growth rate of
osteosarcoma were influenced by hsa-miR-889-3p in xenograft models. To further explore its potential mechanism, the target gene of hsa-miR-889-3p was predicted. Furthermore, hsa-miR-889-3p was confirmed to inhibit the expression of myeloid cell nuclear
differentiation antigen (MNDA) in a targeted manner. In conclusion, hsa-miR-889-3p could promote the proliferation of
osteosarcoma through inhibiting MNDA expression, which provides a potential therapeutic strategy in treatment for
osteosarcoma.