Hypoxia increases the expression of stem cell markers in human osteosarcoma cells

Osteosarcoma (OS) is the most common primary malignant tumor of bone. It is a common phenomenon that osteosarcoma cells have a hypoxic microenvironment. Hypoxia can dedifferentiate cells of several malignant tumor types into stem cell-like phenotypes. However, the role of hypoxia in stemness induction and the expression of cancer stem cell (CSC) markers in human osteosarcoma cells has not been reported. The present study examined the effects of hypoxia on stem-like cells in the human osteosarcoma MNNG/HOS cells. Under the incubation with 1% oxygen, the expression of CSCs markers (Oct-4, Nanog and CD133) in MNNG/HOS cells were increased. Moreover, MNNG/HOS cells cultured under hypoxic conditions were more likely to proliferate into spheres and resulted in larger xenograft tumor. Hypoxia also increased the mRNA and protein levels of hypoxia-inducible factor (HIF)-1 alpha. Then rapamycin was used, which has been shown to lower HIF-1 alpha protein level, to inhibit the hypoxic response. Rapamycin suppressed the expression of HIF-1 alpha protein and CSCs markers (Oct4, Nanog and CD133) in MNNG/HOS cells. In addition, pretreatment with rapamycin reduced the efficiency of MNNG/HOS cells in forming spheres and xenograft tumors. The results demonstrated that hypoxia (1% oxygen) can dedifferentiate some of the MNNG/HOS cells into stem cell-like phenotypes, and that the mTOR signaling pathway participates in this process via regulating the expression of HIF-1 alpha protein.

Automated summary

Hypoxia can induce stem cell-like phenotypes in some osteosarcoma cells, with increased expression of CSC markers and enhanced sphere formation and xenograft tumor growth. Rapamycin, by suppressing HIF-1 alpha protein levels, inhibits the hypoxic response and reduces stem cell marker expression, leading to decreased sphere and xenograft tumor formation efficiency in osteosarcoma cells.