Evidence map›Paper›PMID 33468168›Full record

ArticleJournal of nanobiotechnology2021

Few-layer graphene induces both primary and secondary genotoxicity in epithelial barrier models in vitro.

Michael J Burgum, Martin J D Clift, Stephen J Evans, Nicole Hondow, Afshin Tarat, Gareth J Jenkins, Shareen H Doak

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
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  8. Article
  9. Genotoxicity of Graphene-Based Materials.Nanomaterials (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Michael J BurgumInstitute of Life Science, Swansea University Medical School, Swansea University, Singleton Park, Swansea, SA2 8PP, Wales, UK.ORCID http://orcid.org/0000-0002-3123-8914
Martin J D CliftInstitute of Life Science, Swansea University Medical School, Swansea University, Singleton Park, Swansea, SA2 8PP, Wales, UK.ORCID http://orcid.org/0000-0001-6133-3368
Stephen J EvansInstitute of Life Science, Swansea University Medical School, Swansea University, Singleton Park, Swansea, SA2 8PP, Wales, UK.
Nicole HondowSchool of Chemical and Process Engineering, University of Leeds, Leeds, LS2 9JT, UK.
Afshin TaratPerpetuus Carbon Technologies, Unit B1, Olympus Court, Millstream Way, Llansamlet, Swansea Vale, SA70AQ, UK.
Gareth J JenkinsInstitute of Life Science, Swansea University Medical School, Swansea University, Singleton Park, Swansea, SA2 8PP, Wales, UK.
Shareen H DoakInstitute of Life Science, Swansea University Medical School, Swansea University, Singleton Park, Swansea, SA2 8PP, Wales, UK. s.h.doak@swansea.ac.uk.ORCID http://orcid.org/0000-0002-6753-1987
Swansea University · GBOlympus (United Kingdom) · GBUniversity of Leeds · GB

Funding

European Social Fund 80815National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/R001375/1
6 · The paper itself

Abstract

backgroundToxicological evaluation of engineered nanomaterials (ENMs) is essential for occupational health and safety, particularly where bulk manufactured ENMs such as few-layer graphene (FLG) are concerned. Additionally, there is a necessity to develop advanced in vitro models when testing ENMs to provide a physiologically relevant alternative to invasive animal experimentation. The aim of this study was to determine the genotoxicity of non-functionalised (neutral), amine- and carboxyl-functionalised FLG upon both human-transformed type-I (TT1) alveolar epithelial cell monocultures, as well as co-cultures of TT1 and differentiated THP-1 monocytes (d.THP-1 (macrophages)).

resultsIn monocultures, TT1 and d.THP-1 macrophages showed a statistically significant (p < 0.05) cytotoxic response with each ENM following 24-h exposures. Monoculture genotoxicity measured by the in vitro cytokinesis blocked micronucleus (CBMN) assay revealed significant (p < 0.05) micronuclei induction at 8 µg/ml for amine- and carboxyl-FLG. Transmission electron microscopy (TEM) revealed ENMs were internalised by TT1 cells within membrane-bound vesicles. In the co-cultures, ENMs induced genotoxicity in the absence of cytotoxic effects. Co-cultures pre-exposed to 1.5 mM N-acetylcysteine (NAC), showed baseline levels of micronuclei induction, indicating that the genotoxicity observed was driven by oxidative stress.

conclusionsTherefore, FLG genotoxicity when examined in monocultures, results in primary-indirect DNA damage; whereas co-cultured cells reveal secondary mechanisms of DNA damage.

Indexed as

Alveolar Epithelial CellsAnimalsCell DifferentiationCell LineCell SurvivalCoculture TechniquesDNA DamageFilaggrin ProteinsGraphiteHumansMacrophagesMutagenicity TestsNanostructuresOxidative StressTHP-1 CellsFilaggrin ProteinsFLG protein, humanGraphite

Identifiers

PMID33468168
PMCPMC7816456
OpenAlexW3122371299

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.