Evidence map›Paper›PMID 34764412›Full record

ArticleScientific reports2021

Factors that influence the quality of metabolomics data in in vitro cell toxicity studies: a systematic survey.

Marta Moreno-Torres, Guillem García-Llorens, Erika Moro, Rebeca Méndez, Guillermo Quintás, José Vicente Castell

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Trial
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  4. Article
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  7. Endocrine-disrupting compounds and metabolomic reprogramming in breast cancer.Journal of biochemical and molecular toxicology · 2023
    Review
  8. Article
  9. Article
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  11. Review
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

6 authors.

Marta Moreno-TorresUnidad de Hepatología Experimental y Trasplante Hepático, Health Research Institute Hospital La Fe, Valencia, Spain.
Guillem García-LlorensUnidad de Hepatología Experimental y Trasplante Hepático, Health Research Institute Hospital La Fe, Valencia, Spain.
Erika MoroUnidad de Hepatología Experimental y Trasplante Hepático, Health Research Institute Hospital La Fe, Valencia, Spain.
Rebeca MéndezUnidad de Hepatología Experimental y Trasplante Hepático, Health Research Institute Hospital La Fe, Valencia, Spain.
Guillermo QuintásHealth and Biomedicine, LEITAT Technological Center, Barcelona, Spain. gquintas@leitat.org.
José Vicente CastellUnidad de Hepatología Experimental y Trasplante Hepático, Health Research Institute Hospital La Fe, Valencia, Spain.

Funding

European Union's Horizon 2020 681002Generalitat Valenciana ACIF/2019/145Ministerio español de Ciencia e Innovación IJC2018-036209-I
6 · The paper itself

Abstract

REACH (Registration, Evaluation, Authorization and Restriction of Chemicals) is a global strategy and regulation policy of the EU that aims to improve the protection of human health and the environment through the better and earlier identification of the intrinsic properties of chemical substances. It entered into force on 1st June 2007 (EC 1907/2006). REACH and EU policies plead for the use of robust high-throughput "omic" techniques for the in vitro investigation of the toxicity of chemicals that can provide an estimation of their hazards as well as information regarding the underlying mechanisms of toxicity. In agreement with the 3R's principles, cultured cells are nowadays widely used for this purpose, where metabolomics can provide a real-time picture of the metabolic effects caused by exposure of cells to xenobiotics, enabling the estimations about their toxicological hazards. High quality and robust metabolomics data sets are essential for precise and accurate hazard predictions. Currently, the acquisition of consistent and representative metabolomic data is hampered by experimental drawbacks that hinder reproducibility and difficult robust hazard interpretation. Using the differentiated human liver HepG2 cells as model system, and incubating with hepatotoxic (acetaminophen and valproic acid) and non-hepatotoxic compounds (citric acid), we evaluated in-depth the impact of several key experimental factors (namely, cell passage, processing day and storage time, and compound treatment) and instrumental factors (batch effect) on the outcome of an UPLC-MS metabolomic analysis data set. Results showed that processing day and storage time had a significant impact on the retrieved cell's metabolome, while the effect of cell passage was minor. Meta-analysis of results from pathway analysis showed that batch effect corrections and quality control (QC) measures are critical to enable consistent and meaningful estimations of the effects caused by compounds on cells. The quantitative analysis of the changes in metabolic pathways upon bioactive compound treatment remained consistent despite the concurrent causes of metabolomic data variation. Thus, upon appropriate data retrieval and correction and by an innovative metabolic pathway analysis, the metabolic alteration predictions remained conclusive despite the acknowledged sources of variability.

Indexed as

AcetaminophenCell Line, TumorChemical and Drug Induced Liver InjuryCitric AcidHep G2 CellsHumansLiverMetabolic Networks and PathwaysMetabolomeMetabolomicsQuality ControlReproducibility of ResultsValproic AcidXenobioticsAcetaminophenCitric AcidValproic AcidXenobiotics

Identifiers

PMID34764412
PMCPMC8586040

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Registered trials

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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.