Evidence map›Paper›PMID 34202329›Full record

ArticleInternational journal of molecular sciences2021

Combinatory Effects of Cerium Dioxide Nanoparticles and Acetaminophen on the Liver-A Case Study of Low-Dose Interactions in Human HuH-7 Cells.

Benjamin C Krause, Fabian L Kriegel, Victoria Tartz, Harald Jungnickel, Philipp Reichardt, Ajay Vikram Singh, Peter Laux, Mohamed Shemis, Andreas Luch

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. ZnO/CeOJournal of functional biomaterials · 2022
    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

9 authors.

Benjamin C KrauseDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.ORCID 0000-0003-4684-2206
Fabian L KriegelDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.ORCID 0000-0003-1536-2840
Victoria TartzDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.
Harald JungnickelDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.
Philipp ReichardtDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.
Ajay Vikram SinghDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.ORCID 0000-0002-9875-7727
Peter LauxDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.
Mohamed ShemisDepartment of Biochemistry & Molecular Biology, Theodor Bilharz Research Institute, Warak El-Hadar, Kornish El-Nile, P.O. Box 30 Imbaba, Giza 12411, Egypt.ORCID 0000-0003-2493-7466
Andreas LuchDepartment of Chemical & Product Safety, German Federal Institute for Risk Assessment, Max-Dohrn-Straße 8-10, 10589 Berlin, Germany.

Funding

Bundesinstitut für Risikobewertung SFP1322-642Bundesministerium für Bildung und Forschung BfR-CPS-08-1334-230, 01DH17052Science and Technology Development Fund STDF-DAAD 23052
6 · The paper itself

Abstract

The interactions between pharmaceuticals and nanomaterials and its potentially resulting toxicological effects in living systems are only insufficiently investigated. In this study, two model compounds, acetaminophen, a pharmaceutical, and cerium dioxide, a manufactured nanomaterial, were investigated in combination and individually. Upon inhalation, cerium dioxide nanomaterials were shown to systemically translocate into other organs, such as the liver. Therefore we picked the human liver cell line HuH-7 cells as an in vitro system to investigate liver toxicity. Possible synergistic or antagonistic metabolic changes after co-exposure scenarios were investigated. Toxicological data of the water soluble tetrazolium (WST-1) assay for cell proliferation and genotoxicity assessment using the Comet assay were combined with an untargeted as well as a targeted lipidomics approach. We found an attenuated cytotoxicity and an altered metabolic profile in co-exposure experiments with cerium dioxide, indicating an interaction of both compounds at these endpoints. Single exposure against cerium dioxide showed a genotoxic effect in the Comet assay. Conversely, acetaminophen exhibited no genotoxic effect. Comet assay data do not indicate an enhancement of genotoxicity after co-exposure. The results obtained in this study highlight the advantage of investigating co-exposure scenarios, especially for bioactive substances.

Indexed as

NanoparticlesAcetaminophenBiological TransportCell Line, TumorCeriumDNA DamageDrug SynergismHumansLiverMetabolomeMetabolomicsParticle SizeSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAcetaminophenceric oxideCeriumacetaminophencerium dioxideHuH-7 cellslivermetabolomicsnanoparticlesToF-SIMS

Identifiers

PMID34202329
PMCPMC8268126

What OpenQuestion holds

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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.