Evidence map›Paper›PMID 34395098›Full record

ArticlePeerJ2021

HepGentox: a novel promising HepG2 reportergene-assay for the detection of genotoxic substances in complex mixtures.

Elisabeth Pinter, Christina Friedl, Alexandra Irnesberger, Thomas Czerny, Tina Piwonka, Alfonso Peñarroya, Manfred Tacker, Elisabeth Riegel

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 62% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

Elisabeth PinterDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Christina FriedlDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Alexandra IrnesbergerDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Thomas CzernyDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Tina PiwonkaDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Alfonso PeñarroyaDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Manfred TackerDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
Elisabeth RiegelDepartement of Applied Life Sciences, University of Applied Sciences Vienna, FH Campus Wien, Vienna, Austria.
FH Campus Wien · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn risk assessment, genotoxicity is a key factor to determine the safety for the consumer. Most

methodsA HepG2 liver cell line was characterized for its suitability for genotoxicity assessment. For this, a luciferase based reporter gene assay revolving around the p53 pathway was validated for the analysis of pure substances and of complex mixtures. Further, the cell's capability to detect genotoxins correctly with and without an exogenous metabolizing system, namely rat liver S9, was assessed.

resultsThe assay proved to have a high toxicological sensitivity (87.5%) and specificity (94%). Further, the endogenous metabolizing system of the HepG2 cells was able to detect some genotoxins, which are known to depend on an enzymatic system. When complex mixtures were added this did not lead to any adverse effects concerning the assays performance and cytotoxicity was not an issue. DISCUSSION: The HepGentox proved to have a high toxicological sensitivity and specificity for the tested substances, with similar or even lower lowest effective concentration (LEC) values, compared to other regulatory mammalian assays. This combines some important aspects in one test system, while also being less time and material consuming and covering several genotoxicity endpoints. As the assay performs well with and without an exogenous metabolizing system, no animal liver fractions have to be used, which application is discussed controversially and is considered to be expensive and laborious in sample testing. Because of this, the HepGentox is suitable for a cost-efficient first screening approach to obtain important information with human cells for further approaches, with a relatively fast and easy method. Therefore, the HepGentox is a promising assay to detect genotoxic substances correctly in complex mixtures even at low concentrations, with the potential for a high throughput application. In a nutshell, as part of an

Indexed as

Complex MixturesFood Contact MaterialsGenotoxicityHepG2Metabolizationp53Reportergene-assay

Identifiers

PMID34395098
PMCPMC8323594
OpenAlexW3183534671

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.