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Long-Term Exposure to Real-Life Polyethylene Terephthalate Nanoplastics Induces Carcinogenesis In Vitro
Summary
In a lab study, human lung cells exposed to PET nanoplastics (the same plastic used in water bottles) for 30 weeks developed signs of cancer, including DNA damage, the ability to grow without normal anchoring, and increased activity of cancer-related genes. These findings suggest that long-term, chronic exposure to nanoplastics through breathing could carry serious cancer risks that short-term safety tests would miss.
Micro/nanoplastics (MNPLs) are environmental contaminants originating mainly from plastic waste degradation that pose potential health risks. Inhalation is a major exposure route, as evidenced by their detection in human lungs, with polyethylene terephthalate (PET) among the most abundant particles in respiratory airways. However, the harmful effects of particle bioaccumulation remain unclear, as chronic effects are understudied. To assess long-term effects, specifically carcinogenic effects, BEAS-2B cells were exposed to PET-NPLs for 30 weeks. Genotoxicity, carcinogenic phenotypic hallmarks, and a panel of genes and pathways associated with cell transformation and lung cancer were examined and compared across three exposure durations. No significant effects were observed after 24 h or 15 weeks of exposure. However, a 30-week exposure led to increased genotoxic damage, anchorage-independent growth, and invasive potential. Transcriptomic analysis showed the upregulation of several oncogenes and lung cancer-associated genes at the end of the exposure. Further analysis revealed an increase in differentially expressed genes over time and a temporal gradient of lung cancer-related genes. Altogether, the data suggest PET-NPLs' potential carcinogenicity after extended exposure, highlighting serious long-term health risks of MNPLs. Assessing their carcinogenic risks under chronic scenarios of exposure is crucial to addressing knowledge gaps and eventually developing preventive policies.