Evidence map›Paper›PMID 32700163›Full record

ArticleArchives of toxicology2020

Following the adverse outcome pathway from micronucleus to cancer using H2B-eGFP transgenic healthy stem cells.

Bastian Niklas Hölzel, Kurt Pfannkuche, Bernhard Allner, Hans Thomas Allner, Jürgen Hescheler, Daniel Derichsweiler, Henner Hollert, Andreas Schiwy, Julia Brendt, Michael Schaffeld and 2 more

Abstract read
In one paragraph

Article in Archives of toxicology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

12 authors.

Bastian Niklas HölzelGOBIO GmbH, Institute for Ecology of Waters and Applied Biology, Scheidertalstraße 69a, 65326, Aarbergen, Hesse, Germany. bastianhoelzel@gobio-gmbh.de.
Kurt PfannkucheMedical Faculty, Center for Physiology and Pathophysiology, University of Cologne, Robert Koch Str. 39, 50923, Cologne, North Rhine-Westphalia, Germany. Kurt.Pfannkuche@uni-koeln.de.ORCID http://orcid.org/0000-0002-4284-774X
Bernhard AllnerGOBIO GmbH, Institute for Ecology of Waters and Applied Biology, Scheidertalstraße 69a, 65326, Aarbergen, Hesse, Germany.
Hans Thomas AllnerGOBIO GmbH, Institute for Ecology of Waters and Applied Biology, Scheidertalstraße 69a, 65326, Aarbergen, Hesse, Germany.
Jürgen HeschelerMedical Faculty, Center for Physiology and Pathophysiology, University of Cologne, Robert Koch Str. 39, 50923, Cologne, North Rhine-Westphalia, Germany.
Daniel DerichsweilerMedical Faculty, Center for Physiology and Pathophysiology, University of Cologne, Robert Koch Str. 39, 50923, Cologne, North Rhine-Westphalia, Germany.
Henner HollertEvolutionary Ecology and Environmental Toxicology, Goethe University Frankfurt Biologicum, Max-von-Laue-Straße 13, 60323, Frankfurt am Main, Hesse, Germany.
Andreas SchiwyEvolutionary Ecology and Environmental Toxicology, Goethe University Frankfurt Biologicum, Max-von-Laue-Straße 13, 60323, Frankfurt am Main, Hesse, Germany.
Julia BrendtInstitute for Environmental Research (Bio V), RWTH Aachen University, Worringerweg 1, 52062, Aachen, North Rhine-Westphalia, Germany.
Michael SchaffeldInstitute for Molecular Physiology, Johannes Gutenberg-University Mainz, Johann-Joachim Becher-Weg 7, 55122, Mainz, Rhineland Palatinate, Germany.
Alexander FroschauerFaculty of Biology, Applied Biology, Technische Universität Dresden, Zellescher Weg 20b, 01069, Dresden, Saxony, Germany.
Petra Stahlschmidt-AllnerGOBIO GmbH, Institute for Ecology of Waters and Applied Biology, Scheidertalstraße 69a, 65326, Aarbergen, Hesse, Germany. stahlschmidt@gobio-gmbh.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vitro assessment of genotoxicity as an early warning tool for carcinogenicity mainly relies on recording cytogenetic damages (micronuclei, nucleoplasmic bridges) in tumour-derived mammalian cell lines like V79 or CHO. The forecasting power of the corresponding standardised test is based on epidemiological evidence between micronuclei frequencies and cancer incidence. As an alternative to destructive staining of nuclear structures a fish stem cell line transgenic for a fusion protein of histone 2B (H2B) and enhanced green fluorescent protein (eGFP) was established. The cells are derived from koi carp brain (KCB) and distinguish from mammalian culturable cells by non-tumour-driven self-renewal. This technology enables the analysis of genotoxic- and malign downstream effects in situ in a combined approach. In proof-of concept-experiments, we used known carcinogens (4-Nitroquinoline 1-oxide, colchicine, diethylstilbestrol, ethyl methanesulfonate) and observed a significant increase in micronuclei (MNi) frequencies in a dose-dependent manner. The concentration ranges for MNi induction were comparable to human/mammalian cells (i.e. VH-16, CHL and HepG2). Cannabidiol caused the same specific cytogenetic damage pattern as observed in human cells, in particular nucleoplasmic bridges. Metabolic activation of aflatoxin B1 and cyclophosphamide could be demonstrated by pre-incubation of the test compounds using either conventional rat derived S9 mix as well as an in vitro generated biotechnological alternative product ewoS9R. The presented high throughput live H2B-eGFP imaging technology using non-transformed stem cells opens new perspectives in the field of in vitro toxicology. The technology offers experimental access to investigate the effects of carcinogens on cell cycle control, gene expression pattern and motility in the course of malign transformation. The new technology enables the definition of Adverse Outcome Pathways leading to malign cell transformation and contributes to the replacement of animal testing. Summary: Complementation of genotoxicity testing by addressing initiating events leading to malign transformation is suggested. A vertebrate cell model showing "healthy" stemness is recommended, in contrast to malign transformed cells used in toxicology/oncocology.

Indexed as

Adverse Outcome PathwaysMutagenicity TestsAnimalsAnimals, Genetically ModifiedCarcinogensCell LineCell NucleusCells, CulturedCell Transformation, NeoplasticCyclophosphamideDNA DamageEthyl MethanesulfonateGreen Fluorescent ProteinsHistonesHumansMutagensCarcinogensCyclophosphamideenhanced green fluorescent proteinEthyl MethanesulfonateGreen Fluorescent ProteinsHistonesMutagensAOP for malign transformationMicronucleus testNon-destructive live-cell imaging technology

Identifiers

PMID32700163
PMCPMC7415759

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.