4.7 Article

Immunotoxicity, genotoxicity and epigenetic toxicity of nanomaterials: New strategies for toxicity testing?

Journal

FOOD AND CHEMICAL TOXICOLOGY
Volume 109, Issue -, Pages 797-811

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2017.08.030

Keywords

Nanomaterials; Nanotoxicology; Immunotoxicity; Genotoxicity; Epigenetic toxicity; Testing strategy

Funding

  1. NRC NorNANoREG [239199/O70]
  2. EC FP7 QualityNano [INFRA-2010-262163, 214547-2]
  3. Norwegian Institute for Air Research [NILU-TAF-276, NILU-TAF-279]
  4. Horizon NANoREG2 project [H2020-NMP-2014-2015-646221]
  5. HISENTS project [H2020-NMP-2015-685817]
  6. ERA-NET EuroNanoMed II GEMNS project
  7. ERA-NET EuroNanoMed II INNOCENT project
  8. Slovak Research and Development Agency [APVV-0404-11]
  9. ITMS project from the European Regional Development Fund [26240120033]

Ask authors/readers for more resources

The unique properties of nanomaterials (NMs) are beneficial in numerous industrial and medical applications. However, they could also induce unintended effects. Thus, a proper strategy for toxicity testing is essential in human hazard and risk assessment. Toxicity can be tested in vivo and in vitro; in compliance with the 3Rs, alternative strategies for in vitro testing should be further developed for NMs. Robust, standardized methods are of great importance in nanotoxicology, with comprehensive material characterization and uptake as an integral part of the testing strategy. Oxidative stress has been shown to be an underlying mechanism of possible toxicity of NMs, causing both immunotoxicity and genotoxicity. For testing NMs in vitro, a battery of tests should be performed on cells of human origin, either cell lines or primary cells, in conditions as close as possible to an in vivo situation. Novel toxicity pathways, particularly epigenetic modification, should be assessed along with conventional toxicity testing methods. However, to initiate epigenetic toxicity screens for NM exposure, there is a need to better understand their adverse effects on the epigenome, to identify robust and reproducible causal links between exposure, epigenetic changes and adverse phenotypic endpoints, and to develop improved assays to monitor epigenetic toxicity. (C) 2017 The Authors. Published by Elsevier Ltd.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available