Literature DB >> 28746895

Effects on human bronchial epithelial cells following low-dose chronic exposure to nanomaterials: A 6-month transformation study.

Santosh Phuyal1, Mayes Kasem1, Laura Rubio2, Hanna L Karlsson3, Ricard Marcos4, Vidar Skaug1, Shanbeh Zienolddiny5.   

Abstract

The most plausible exposure route to manufactured nanomaterials (MNM) remains pulmonary inhalation. Yet, few studies have attempted to assess carcinogenic properties in vitro following long-term exposure of human pulmonary cells to low and occupationally relevant doses. The most advanced in vitro tests for carcinogenicity, the cell transformation assay (CTA), rely mostly on rodent cells and short-term exposure. We hypothesized that long-term exposure of human bronchial epithelial cells with a normal phenotype could be a valuable assay for testing carcinogenicity of nanomaterials. Therefore, this study (performed within the framework of the FP7-NANoREG project) assessed carcinogenic potential of chronic exposure (up to 6months) to low doses of multi-walled carbon nanotubes (MWCNT, NM-400 and NM-401) and TiO2 materials (NM62002 and KC7000). In order to harmonize and standardize the experiments, standard operating protocols of MNM dispersion (NANOGENOTOX) were used by three different NANoREG project partners. All nanomaterials showed low cytotoxicity in short-term tests for the tested doses (0.96 and 1.92μg/cm2). During long-term exposure, however, NM-401 clearly affected cell proliferation. In contrast, no cell transformation was observed for NM-401 by any of the partners. NM-400 and NM62002 formed some colonies after 3months. We conclude that agglomerated NM-401 in low doses affect cell proliferation but do not cause cell transformation in the CTA assay used.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Carcinogenicity; Cell transformation; Cytotoxicity; HBEC-3KT cells; Long-term exposure; Manufactured nanomaterials

Mesh:

Substances:

Year:  2017        PMID: 28746895     DOI: 10.1016/j.tiv.2017.07.016

Source DB:  PubMed          Journal:  Toxicol In Vitro        ISSN: 0887-2333            Impact factor:   3.500


  5 in total

1.  Individual and combined toxicity of carboxylic acid functionalized multi-walled carbon nanotubes and benzo a pyrene in lung adenocarcinoma cells.

Authors:  Mansour Rezazadeh Azari; Yousef Mohammadian; Jalal Pourahmad; Fariba Khodagholi; Habibollah Peirovi; Yadollah Mehrabi; Meisam Omidi; Athena Rafieepour
Journal:  Environ Sci Pollut Res Int       Date:  2019-03-16       Impact factor: 4.223

2.  Multiwalled Carbon Nanotubes Induce Fibrosis and Telomere Length Alterations.

Authors:  Mayes Alswady-Hoff; Johanna Samulin Erdem; Mona Aleksandersen; Kristine Haugen Anmarkrud; Øivind Skare; Fang-Chin Lin; Vincent Simensen; Yke Jildouw Arnoldussen; Vidar Skaug; Erik Ropstad; Shanbeh Zienolddiny-Narui
Journal:  Int J Mol Sci       Date:  2022-05-26       Impact factor: 6.208

3.  Long-Term Exposure to Nanosized TiO2 Triggers Stress Responses and Cell Death Pathways in Pulmonary Epithelial Cells.

Authors:  Mayes Alswady-Hoff; Johanna Samulin Erdem; Santosh Phuyal; Oskar Knittelfelder; Animesh Sharma; Davi de Miranda Fonseca; Øivind Skare; Geir Slupphaug; Shanbeh Zienolddiny
Journal:  Int J Mol Sci       Date:  2021-05-19       Impact factor: 5.923

4.  Toxicity of TiO2 Nanoparticles: Validation of Alternative Models.

Authors:  Mélanie M Leroux; Zahra Doumandji; Laetitia Chézeau; Laurent Gaté; Sara Nahle; Romain Hocquel; Vadim Zhernovkov; Sylvie Migot; Jafar Ghanbaja; Céline Bonnet; Raphaël Schneider; Bertrand H Rihn; Luc Ferrari; Olivier Joubert
Journal:  Int J Mol Sci       Date:  2020-07-09       Impact factor: 5.923

5.  miR221 regulates cell migration by targeting annexin a1 expression in human mesothelial MeT-5A cells neoplastic-like transformed by multi-walled carbon nanotube.

Authors:  Li Ju; Lijin Zhu; Hao Wu; Min Yu; Xianhong Yin; Zhenyu Jia; Lingfang Feng; Shibo Ying; Hailing Xia; Shuzhi Zhang; Jianlin Lou; Jun Yang
Journal:  Genes Environ       Date:  2021-08-02
  5 in total

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