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Small Particles, Big Problems: Polystyrene nanoparticles induce DNA damage, oxidative stress, migration, and mitogenic pathways predominantly in non-malignant lung cells

Journal of Hazardous Materials 2025 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 63 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Büsra Ernhofer, Andreas Spittler, Franziska Ferk, Miroslav Mišík, Martha Zylka, Lisa Glatt, Kristiina Boettiger, Anna Solta, Dominik Kirchhofer, Gerald Timelthaler, Zsolt Megyesfalvi, Verena Kopatz, Heinrich Kovar, Siegfried Knasmüller, Clemens Aigner, Lukas Kenner, Balázs Döme, Karin Schelch

Summary

Researchers found that polystyrene nanoparticles caused more DNA damage, oxidative stress, and cell migration in normal lung cells than in lung cancer cells. The healthy cells absorbed and processed the nanoparticles more actively, which paradoxically made them more vulnerable to damage. This is an important finding because it suggests that everyday nanoplastic exposure from the environment may pose greater risks to healthy lung tissue than previously assumed.

Polymers
Body Systems

Polystyrene micro- and nanoplastics (PS-MNPs) are emerging environmental pollutants with potential implications for human health. This study investigated the cytotoxic effects of PS particles by using two different sizes of PS-MNPs (0.25 µm and 1 µm) on non-small cell lung cancer (A549, H460), small cell lung cancer (DMS53, H372), and normal lung epithelial (BEAS-2B) cells as well as on human-derived lung organoids. Neither PS-MPs nor PS-NPs interfered with cell viability or proliferation at lower concentrations (< 30 µg/cm2, equivalent to 50 µg/ml). Intracellular kinetic assays revealed that non-malignant (BEAS-2B) lung cells had the strongest turnover of PS-NPs compared to malignant cells. Since PS-NPs exhibited more pronounced cellular effects, additional analyses focused on their impact. Furthermore, we observed significantly increased migration, prolonged S-phase arrest with induced DNA damage, and oxidative stress in non-malignant (BEAS-2B) lung cells. Thus, our data suggest that BEAS-2B cells exhibit the highest sensitivity to PS-NPs. These cells displayed decreased base excision repair capacity and increased activation of survival pathways including AKT and ERK phosphorylation after PS-NP treatment. PS-NP internalization and increase of signal pathways were validated in a physiological lung organoid setting. Our findings suggest that while PS-NPs do not significantly affect the malignant behavior of cancer cells, they could promote malignant features in normal lung cells through the induction of survival pathways, migration, and altered stress response mechanisms.

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