Evidence map›Paper›PMID 28415582›Full record

ArticleOncotarget2017

Respiratory status determines the effect of emodin on cell viability.

Verónica I Dumit, Ralf M Zerbes, Stephanie Kaeser-Pebernard, Michal Rackiewicz, Mona T Wall, Christine Gretzmeier, Victoria Küttner, Martin van der Laan, Ralf J Braun, Jörn Dengjel

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.5field-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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

10 authors at 4 institutions in 2 countries.

Verónica I DumitFreiburg Institute for Advanced Studies (FRIAS), University of Freiburg, Freiburg, Germany.
Ralf M ZerbesInstitute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Stephanie Kaeser-PebernardDepartment of Biology, University of Fribourg, Fribourg, Switzerland.
Michal RackiewiczCenter for Biological Systems Analysis (ZBSA), Freiburg, Germany.
Mona T WallFreiburg Institute for Advanced Studies (FRIAS), University of Freiburg, Freiburg, Germany.
Christine GretzmeierCenter for Biological Systems Analysis (ZBSA), Freiburg, Germany.
Victoria KüttnerCenter for Biological Systems Analysis (ZBSA), Freiburg, Germany.
Martin van der LaanInstitute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Ralf J BraunInstitute of Cell Biology, University of Bayreuth, Bayreuth, Germany.
Jörn DengjelFreiburg Institute for Advanced Studies (FRIAS), University of Freiburg, Freiburg, Germany.
University of Freiburg · DEUniversity Medical Center Freiburg · DEUniversity of Bayreuth · DEUniversity of Fribourg · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The anthraquinone emodin has been shown to have antineoplastic properties and a wealth of unconnected effects have been linked to its use, most of which are likely secondary outcomes of the drug treatment. The primary activity of emodin on cells has remained unknown. In the present study we demonstrate dramatic and extensive effects of emodin on the redox state of cells and on mitochondrial homeostasis, irrespectively of the cell type and organism, ranging from the yeast Saccharomyces cerevisiae to human cell lines and primary cells. Emodin binds to redox-active enzymes and its effectiveness depends on the oxidative and respiratory status of cells. We show that cells with efficient respiratory metabolism are less susceptible to emodin, whereas cells under glycolytic metabolism are more vulnerable to the compound. Our findings indicate that emodin acts in a similar way as known uncouplers of the mitochondrial electron transport chain and causes oxidative stress that particularly disturbs cancer cells.

Indexed as

A549 CellsCaco-2 CellsCell ProliferationCells, CulturedCell SurvivalEmodinFibroblastsHeLa CellsHumansMCF-7 CellsMitochondriaNeoplasmsPhosphorylationProtein Kinase InhibitorsProtein KinasesProteomicsEmodinProtein Kinase InhibitorsProtein KinasesReactive Oxygen Speciesanthraquinonechemoproteomicscomplex Imitochondriareactive oxygen species

Identifiers

PMID28415582
PMCPMC5514923
OpenAlexW2597944979

What OpenQuestion holds

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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.