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Effects of polystyrene nano- and microplastics on human breast epithelial cells and human breast cancer cells

Heliyon 2024 19 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 60 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Maximilian Schnee, Mareike Sieler, Jessica Dörnen, Thomas Dittmar

Summary

Researchers tested how polystyrene nano- and microplastics affect both normal human breast cells and breast cancer cells in the lab. The plastic particles were absorbed by both cell types and caused slight but significant increases in cell growth and migration, behaviors associated with cancer progression. While this is a lab study, it raises questions about whether microplastic accumulation in breast tissue could influence cancer development.

Polymers

The continuous littering of the environment with plastic and the resulting nano- and microplastics produced from various processes are ever-increasing problems. These materials also affect humans, as the absorption and accumulation of nano- and microplastics and their effects on health have thus far been rarely researched, which also applies to cancer. In the present study, the absorption of different sizes of polystyrene (PS) nano- and microplastics (PS particles) into human breast epithelial cells and human breast cancer cells was investigated. Subsequently, how the proliferation, colony and mammosphere formation abilities, cell fusion and migration of the cells were influenced by the PS particles were investigated. Our data revealed granularity-, dose- and cell line-dependent absorption of the PS particles, with the highest absorption observed in the MDA-MB-231-DSP1-7 cells and the lowest in the M13SV1_Syn1-DSP8-11 cells. Neither the colony-forming ability nor the cell fusion activity increased with the addition of PS particles. In contrast, slight, partially significant stimulatory effects on both proliferation and cell migration were observed, although these effects depended on the particle quantity and size and the cell line used. In summary, PS particles are absorbed by human breast epithelial and human breast cancer cells and influence cells that may be associated with cancer progression.

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