Cargando…

Comparative Study on Nanotoxicity in Human Primary and Cancer Cells

Nanomaterial toxicity tests using normal and cancer cells may yield markedly different results. Here, nanomaterial toxicity between cancer and primary human cells was compared to determine the basic cell line selection criteria for nanomaterial toxicity analyses. Specifically, we exposed two cancer...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, In Young, Kwak, Minjeong, Kim, Jaeseok, Lee, Tae Geol, Heo, Min Beom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955245/
https://www.ncbi.nlm.nih.gov/pubmed/35335806
http://dx.doi.org/10.3390/nano12060993
_version_ 1784676289914863616
author Kim, In Young
Kwak, Minjeong
Kim, Jaeseok
Lee, Tae Geol
Heo, Min Beom
author_facet Kim, In Young
Kwak, Minjeong
Kim, Jaeseok
Lee, Tae Geol
Heo, Min Beom
author_sort Kim, In Young
collection PubMed
description Nanomaterial toxicity tests using normal and cancer cells may yield markedly different results. Here, nanomaterial toxicity between cancer and primary human cells was compared to determine the basic cell line selection criteria for nanomaterial toxicity analyses. Specifically, we exposed two cancer (A549 and HepG2) and two normal cell lines (NHBE and HH) cell lines to SiO(2) nanoparticles (NPs) and evaluated the cytotoxicity (MTS assay), cell death mode, and intracellular NP retention. MTS assay results revealed higher sensitivity of HH cells to SiO(2) NPs than HepG2 cells, while no difference was observed between NHBE and A549 cells. In addition, SiO(2) NPs primarily induced necrosis in all the cell lines. Moreover, we evaluated NP accumulation by treating the cell lines with fluorescein-isothiocyanate-labeled SiO(2) NPs. After 48 h of treatment, less than 10% of A549 and HepG2 cells and more than 30% of NHBE and HH cells contained the labeled NPs. Collectively, our results suggest that cell viability, death mode, and intracellular compound accumulation could be assessed using cancer cells. However, the outcomes of certain investigations, such as intracellular NP retention, may differ between cancer and normal cells.
format Online
Article
Text
id pubmed-8955245
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-89552452022-03-26 Comparative Study on Nanotoxicity in Human Primary and Cancer Cells Kim, In Young Kwak, Minjeong Kim, Jaeseok Lee, Tae Geol Heo, Min Beom Nanomaterials (Basel) Article Nanomaterial toxicity tests using normal and cancer cells may yield markedly different results. Here, nanomaterial toxicity between cancer and primary human cells was compared to determine the basic cell line selection criteria for nanomaterial toxicity analyses. Specifically, we exposed two cancer (A549 and HepG2) and two normal cell lines (NHBE and HH) cell lines to SiO(2) nanoparticles (NPs) and evaluated the cytotoxicity (MTS assay), cell death mode, and intracellular NP retention. MTS assay results revealed higher sensitivity of HH cells to SiO(2) NPs than HepG2 cells, while no difference was observed between NHBE and A549 cells. In addition, SiO(2) NPs primarily induced necrosis in all the cell lines. Moreover, we evaluated NP accumulation by treating the cell lines with fluorescein-isothiocyanate-labeled SiO(2) NPs. After 48 h of treatment, less than 10% of A549 and HepG2 cells and more than 30% of NHBE and HH cells contained the labeled NPs. Collectively, our results suggest that cell viability, death mode, and intracellular compound accumulation could be assessed using cancer cells. However, the outcomes of certain investigations, such as intracellular NP retention, may differ between cancer and normal cells. MDPI 2022-03-17 /pmc/articles/PMC8955245/ /pubmed/35335806 http://dx.doi.org/10.3390/nano12060993 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, In Young
Kwak, Minjeong
Kim, Jaeseok
Lee, Tae Geol
Heo, Min Beom
Comparative Study on Nanotoxicity in Human Primary and Cancer Cells
title Comparative Study on Nanotoxicity in Human Primary and Cancer Cells
title_full Comparative Study on Nanotoxicity in Human Primary and Cancer Cells
title_fullStr Comparative Study on Nanotoxicity in Human Primary and Cancer Cells
title_full_unstemmed Comparative Study on Nanotoxicity in Human Primary and Cancer Cells
title_short Comparative Study on Nanotoxicity in Human Primary and Cancer Cells
title_sort comparative study on nanotoxicity in human primary and cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955245/
https://www.ncbi.nlm.nih.gov/pubmed/35335806
http://dx.doi.org/10.3390/nano12060993
work_keys_str_mv AT kiminyoung comparativestudyonnanotoxicityinhumanprimaryandcancercells
AT kwakminjeong comparativestudyonnanotoxicityinhumanprimaryandcancercells
AT kimjaeseok comparativestudyonnanotoxicityinhumanprimaryandcancercells
AT leetaegeol comparativestudyonnanotoxicityinhumanprimaryandcancercells
AT heominbeom comparativestudyonnanotoxicityinhumanprimaryandcancercells