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Subsequently, the expression of VEGF‑C, BDNF and CCL3 in BMSCs overexpressing miR‑210 or BMSCs suppressing miR‑210 was examined by RT‑qPCR and western blot analyses. BMSCs promoted the migration of NPC, particularly when pre‑cultured with BMSCs for 24 h and co‑cultured with NPCs for 24 h; the miR‑210 expression levels increased under hypoxic conditions. Additionally, the migration of NPCs was also increased when the BMSCs overexpressed miR‑210 compared with the BMSCs transfected with a negative control miR and BMSCs with downregulated m