Genotoxicity and oxidative stress induction by polystyrene nanoparticles in the colorectal cancer cell line HCT116.
Giulia VecchiottiSabrina ColafarinaMassimo AloisiOsvaldo ZariviPiero Di CarloAnna Maria Giuseppina PomaPublished in: PloS one (2021)
The potential risks of environmental nanoparticles (NPs), in particular Polystyrene Nanoparticles (PNPs), is an emerging problem; specifically, the interaction of PNPs with intestinal cells has not been characterized so far. The mechanism by which polystyrene particles are transferred to humans has not yet been clarified, whether directly through ingestion from contaminated food. We evaluated the interaction between PNPs and colorectal adenocarcinoma cells (HCT116). Cells were exposed to different concentrations of PNPs, metabolic activity and the consequent cytotoxic potential were assessed through viability test; we evaluated the PNP genotoxic potential through the Cytokinesis-Block Micronucleus cytome (CBMN cyt) assay. Finally, we detected Reactive Oxygen Species (ROS) production after NPs exposure and performed Western Blot analysis to analyze the enzymes (SOD1, SOD2, Catalase, Glutathione Peroxidase) involved in the cell detoxification process that comes into play during the cell-PNPs interaction. This work analyzes the cyto and genotoxicity of PNPs in the colorectal HCT116 cell line, in particular the potential damage from oxidative stress produced by PNPs inside the cells related to the consequent nuclear damage. Our results show moderate toxicity of PNPs both in terms of ROS production and DNA damage. Further studies will be needed on different cell lines to have a more complete picture of the impact of environmental pollution on human health in terms of PNPs cytotoxicity and genotoxicity.
Keyphrases
- heavy metals
- human health
- risk assessment
- oxidative stress
- induced apoptosis
- cell cycle arrest
- dna damage
- cell death
- reactive oxygen species
- climate change
- squamous cell carcinoma
- signaling pathway
- radiation therapy
- cell therapy
- pi k akt
- oxide nanoparticles
- mesenchymal stem cells
- high intensity
- bone marrow
- dna repair
- amyotrophic lateral sclerosis