Polyethyleneimine coated Fe3O4 magnetic nanoparticles induce autophagy, NF-κB and TGF-β signaling pathway activation in HeLa cervical carcinoma cells via reactive oxygen species generation.
Shuli ManMiao LiJin ZhouHaiyue WangJinyan ZhangLong MaPublished in: Biomaterials science (2019)
Fe3O4 magnetic nanoparticles (MNPs), as one of the most intensively researched NPs, have a range of applications in cancer treatments. In current research, we have focused on the influences of MNPs on cancer cells. We chose polyethyleneimine (PEI) coated MNPs (PEI-MNPs) as a model and they are colloidally stable in biological media. It can be proved that PEI-MNPs result in autophagy induction via mTOR-Akt-p70S6 K and ATG7 signaling pathways. For the first time, we have reported that PEI-MNPs activate both NF-κB and TGF-β signaling, two key pro-inflammatory pathways, in cancer cells. More significantly, we have found that autophagy induction and NF-κB and TGF-β activation can be efficiently suppressed through the inhibition of PEI-MNP dependent reactive oxygen species (ROS) over-production. ROS are deemed as a 'double edge sword' for cancer cells, owing to the cancer-suppressing and cancer-promoting actions. Our findings would be useful for designing MNPs induced ROS anti-cancer strategies or diminishing long-term toxic effects.
Keyphrases
- signaling pathway
- reactive oxygen species
- pi k akt
- magnetic nanoparticles
- cell death
- papillary thyroid
- epithelial mesenchymal transition
- induced apoptosis
- squamous cell
- transforming growth factor
- dna damage
- oxidative stress
- cell proliferation
- cell cycle arrest
- squamous cell carcinoma
- childhood cancer
- high glucose
- young adults
- endothelial cells
- immune response
- stress induced