Publication: Evaluation of tumorigenic potential of CeO<inf>2</inf> and Fe<inf>2</inf>O<inf>3</inf> engineered nanoparticles by a human cell in vitro screening model
Issued Date
2017-04-01
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ISSN
24520748
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2-s2.0-85008235220
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Mahidol University
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SCOPUS
Bibliographic Citation
NanoImpact. Vol.6, (2017), 39-54
Suggested Citation
Todd A. Stueckle, Donna C. Davidson, Raymond Derk, Tiffany G. Kornberg, Diane Schwegler-Berry, Sandra V. Pirela, Glen Deloid, Philip Demokritou, Sudjit Luanpitpong, Yon Rojanasakul, Liying Wang Evaluation of tumorigenic potential of CeO<inf>2</inf> and Fe<inf>2</inf>O<inf>3</inf> engineered nanoparticles by a human cell in vitro screening model. NanoImpact. Vol.6, (2017), 39-54. doi:10.1016/j.impact.2016.11.001 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/42618
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Title
Evaluation of tumorigenic potential of CeO<inf>2</inf> and Fe<inf>2</inf>O<inf>3</inf> engineered nanoparticles by a human cell in vitro screening model
Abstract
© 2016 With rapid development of novel nanotechnologies that incorporate engineered nanomaterials (ENMs) into manufactured products, long-term, low dose ENM exposures in occupational settings is forecasted to occur with potential adverse outcomes to human health. Few ENM human health risk assessment efforts have evaluated tumorigenic potential of ENMs. Two widely used nano-scaled metal oxides (NMOs), cerium oxide (nCeO2) and ferric oxide (nFe2O3) were screened in the current study using a sub-chronic exposure to human primary small airway epithelial cells (pSAECs). Multi-walled carbon nanotubes (MWCNT), a known ENM tumor promoter, was used as a positive control. Advanced dosimetry modeling was employed to ascertain delivered vs. administered dose in all experimental conditions. Cells were continuously exposed in vitro to deposited doses of 0.18 μg/cm2 or 0.06 μg/cm2 of each NMO or MWCNT, respectively, over 6 and 10 weeks, while saline- and dispersant-only exposed cells served as passage controls. Cells were evaluated for changes in several cancer hallmarks, as evidence for neoplastic transformation. At 10 weeks, nFe2O3- and MWCNT-exposed cells displayed a neoplastic-like transformation phenotype with significant increased proliferation, invasion, and soft agar colony formation ability compared to controls. nCeO2-exposed cells showed increased proliferative capacity only. Isolated nFe2O3 and MWCNT clones from soft agar colonies retained their respective neoplastic-like phenotypes. Interestingly, nFe2O3-exposed cells, but not MWCNT cells, exhibited immortalization and retention of the neoplastic phenotype after repeated passaging (12–30 passages) and after cryofreeze and thawing. High content screening and protein expression analyses in acute exposure ENM studies vs. immortalized nFe2O3 cells, and isolated ENM clones, suggested that long-term exposure to the tested ENMs resulted in iron homeostasis disruption, an increased labile ferrous iron pool, and subsequent reactive oxygen species generation, a well-established tumorigenesis promotor. In conclusion, sub-chronic exposure to human pSAECs with a cancer hallmark screening battery identified nFe2O3 as possessing neoplastic-like transformation ability, thus suggesting that further tumorigenic assessment is needed.