Microplastics role in cell migration and distribution during cancer cell division

Standard

Microplastics role in cell migration and distribution during cancer cell division. / Brynzak-Schreiber, Ekaterina; Schögl, Elisabeth; Bapp, Carolin; Cseh, Klaudia; Kopatz, Verena; Jakupec, Michael A; Weber, Andreas; Lange, Tobias; Toca-Herrera, José L; Del Favero, Giorgia; Wadsak, Wolfgang; Kenner, Lukas; Pichler, Verena.

In: CHEMOSPHERE, Vol. 353, 04.2024, p. 141463.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Brynzak-Schreiber, E, Schögl, E, Bapp, C, Cseh, K, Kopatz, V, Jakupec, MA, Weber, A, Lange, T, Toca-Herrera, JL, Del Favero, G, Wadsak, W, Kenner, L & Pichler, V 2024, 'Microplastics role in cell migration and distribution during cancer cell division', CHEMOSPHERE, vol. 353, pp. 141463. https://doi.org/10.1016/j.chemosphere.2024.141463

APA

Brynzak-Schreiber, E., Schögl, E., Bapp, C., Cseh, K., Kopatz, V., Jakupec, M. A., Weber, A., Lange, T., Toca-Herrera, J. L., Del Favero, G., Wadsak, W., Kenner, L., & Pichler, V. (2024). Microplastics role in cell migration and distribution during cancer cell division. CHEMOSPHERE, 353, 141463. https://doi.org/10.1016/j.chemosphere.2024.141463

Vancouver

Brynzak-Schreiber E, Schögl E, Bapp C, Cseh K, Kopatz V, Jakupec MA et al. Microplastics role in cell migration and distribution during cancer cell division. CHEMOSPHERE. 2024 Apr;353:141463. https://doi.org/10.1016/j.chemosphere.2024.141463

Bibtex

@article{0ed667719ed543fdbb5f226ee403375d,
title = "Microplastics role in cell migration and distribution during cancer cell division",
abstract = "Amidst the global plastic pollution crisis, the gastrointestinal tract serves as the primary entry point for daily exposure to micro- and nanoplastics. We investigated the complex dynamics between polystyrene micro- and nanoplastics (PS-MNPs) and four distinct human colorectal cancer cell lines (HT29, HCT116, SW480, and SW620). Our findings revealed a significant size- and concentration dependent uptake of 0.25, 1, and 10 μm PS-MNPs across all cell lines, with HCT116 cells exhibiting the highest uptake rates. During cell division, particles were distributed between mother and daughter cells. Interestingly, we observed no signs of elimination from the cells. Short-term exposure to 0.25 μm particles significantly amplified cell migration, potentially leading to pro-metastatic effects. Particles demonstrated high persistence in 2D and 3D cultures, and accumulation in non-proliferating parts of spheroids, without interfering with cell proliferation or division. Our study unveils the disturbing fact of the persistence and bioaccumulation of MNPs in colorectal cancer cell lines, key toxicological traits under REACH (Regulation concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals). Our observations underscore the potential of MNPs as hidden catalysts for tumor progression, particularly through enhancing cell migration and possibly fueling metastasis - a finding that sheds light on a significant and previously underexplored area of concern.",
author = "Ekaterina Brynzak-Schreiber and Elisabeth Sch{\"o}gl and Carolin Bapp and Klaudia Cseh and Verena Kopatz and Jakupec, {Michael A} and Andreas Weber and Tobias Lange and Toca-Herrera, {Jos{\'e} L} and {Del Favero}, Giorgia and Wolfgang Wadsak and Lukas Kenner and Verena Pichler",
note = "Copyright {\textcopyright} 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.",
year = "2024",
month = apr,
doi = "10.1016/j.chemosphere.2024.141463",
language = "English",
volume = "353",
pages = "141463",
journal = "CHEMOSPHERE",
issn = "0045-6535",
publisher = "Elsevier Limited",

}

RIS

TY - JOUR

T1 - Microplastics role in cell migration and distribution during cancer cell division

AU - Brynzak-Schreiber, Ekaterina

AU - Schögl, Elisabeth

AU - Bapp, Carolin

AU - Cseh, Klaudia

AU - Kopatz, Verena

AU - Jakupec, Michael A

AU - Weber, Andreas

AU - Lange, Tobias

AU - Toca-Herrera, José L

AU - Del Favero, Giorgia

AU - Wadsak, Wolfgang

AU - Kenner, Lukas

AU - Pichler, Verena

N1 - Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.

PY - 2024/4

Y1 - 2024/4

N2 - Amidst the global plastic pollution crisis, the gastrointestinal tract serves as the primary entry point for daily exposure to micro- and nanoplastics. We investigated the complex dynamics between polystyrene micro- and nanoplastics (PS-MNPs) and four distinct human colorectal cancer cell lines (HT29, HCT116, SW480, and SW620). Our findings revealed a significant size- and concentration dependent uptake of 0.25, 1, and 10 μm PS-MNPs across all cell lines, with HCT116 cells exhibiting the highest uptake rates. During cell division, particles were distributed between mother and daughter cells. Interestingly, we observed no signs of elimination from the cells. Short-term exposure to 0.25 μm particles significantly amplified cell migration, potentially leading to pro-metastatic effects. Particles demonstrated high persistence in 2D and 3D cultures, and accumulation in non-proliferating parts of spheroids, without interfering with cell proliferation or division. Our study unveils the disturbing fact of the persistence and bioaccumulation of MNPs in colorectal cancer cell lines, key toxicological traits under REACH (Regulation concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals). Our observations underscore the potential of MNPs as hidden catalysts for tumor progression, particularly through enhancing cell migration and possibly fueling metastasis - a finding that sheds light on a significant and previously underexplored area of concern.

AB - Amidst the global plastic pollution crisis, the gastrointestinal tract serves as the primary entry point for daily exposure to micro- and nanoplastics. We investigated the complex dynamics between polystyrene micro- and nanoplastics (PS-MNPs) and four distinct human colorectal cancer cell lines (HT29, HCT116, SW480, and SW620). Our findings revealed a significant size- and concentration dependent uptake of 0.25, 1, and 10 μm PS-MNPs across all cell lines, with HCT116 cells exhibiting the highest uptake rates. During cell division, particles were distributed between mother and daughter cells. Interestingly, we observed no signs of elimination from the cells. Short-term exposure to 0.25 μm particles significantly amplified cell migration, potentially leading to pro-metastatic effects. Particles demonstrated high persistence in 2D and 3D cultures, and accumulation in non-proliferating parts of spheroids, without interfering with cell proliferation or division. Our study unveils the disturbing fact of the persistence and bioaccumulation of MNPs in colorectal cancer cell lines, key toxicological traits under REACH (Regulation concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals). Our observations underscore the potential of MNPs as hidden catalysts for tumor progression, particularly through enhancing cell migration and possibly fueling metastasis - a finding that sheds light on a significant and previously underexplored area of concern.

U2 - 10.1016/j.chemosphere.2024.141463

DO - 10.1016/j.chemosphere.2024.141463

M3 - SCORING: Journal article

C2 - 38423146

VL - 353

SP - 141463

JO - CHEMOSPHERE

JF - CHEMOSPHERE

SN - 0045-6535

ER -