Evidence map›Paper›PMID 32311219›Full record

ArticleChemMedChem2020

Pentathiepins: A Novel Class of Glutathione Peroxidase 1 Inhibitors that Induce Oxidative Stress, Loss of Mitochondrial Membrane Potential and Apoptosis in Human Cancer Cells.

Steven Behnisch-Cornwell, Siva Sankar Murthy Bandaru, Martin Napierkowski, Lisa Wolff, Muhammad Zubair, Claudia Urbainsky, Christopher Lillig, Carola Schulzke, Patrick J Bednarski

Open access · hybridAbstract read
In one paragraph

Article in ChemMedChem, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  5. GPX1 expression promotes stemness and aggressiveness in myxoid liposarcomas.International journal of biological sciences · 2025
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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

9 authors at 2 institutions in 1 country.

Steven Behnisch-CornwellPharmazeutische/Medizinische Chemie, Institut für Pharmazie, Universität Greifswald, 17489, Greifswald, Germany.
Siva Sankar Murthy BandaruBioanorganische Chemie, Institut für Biochemie, Universität Greifswald, 17489, Greifswald, Germany.
Martin NapierkowskiPharmazeutische/Medizinische Chemie, Institut für Pharmazie, Universität Greifswald, 17489, Greifswald, Germany.
Lisa WolffPharmazeutische/Medizinische Chemie, Institut für Pharmazie, Universität Greifswald, 17489, Greifswald, Germany.
Muhammad ZubairBioanorganische Chemie, Institut für Biochemie, Universität Greifswald, 17489, Greifswald, Germany.
Claudia UrbainskyInstitut für Medizinische Biochemie und Molekulare Biologie, Universitätsmedizin, Universität Greifswald, 17475, Greifswald, Germany.
Christopher LilligInstitut für Medizinische Biochemie und Molekulare Biologie, Universitätsmedizin, Universität Greifswald, 17475, Greifswald, Germany.
Carola SchulzkeBioanorganische Chemie, Institut für Biochemie, Universität Greifswald, 17489, Greifswald, Germany.
Patrick J BednarskiPharmazeutische/Medizinische Chemie, Institut für Pharmazie, Universität Greifswald, 17489, Greifswald, Germany.ORCID 0000-0002-9589-8241
Universität Greifswald · DEUniversitätsmedizin Greifswald · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel class of glutathione peroxidase 1 (GPx1) inhibitors, namely tri- and tetracyclic pentathiepins, has been identified that is approximately 15 times more potent than the most active known GPx1 inhibitor, mercaptosuccinic acid. Enzyme kinetic studies with bovine erythrocyte GPx1 indicate that pentathiepins reversibly inhibit oxidation of the substrate glutathione (GSH). Moreover, no inhibition of superoxide dismutase, catalase, thioredoxin reductase or glutathione reductase was observed at concentrations that effectively inhibit GPx1. As well as potent enzyme inhibitory activity, the pentathiepins show strong anticancer activity in various human cancer cell lines, with IC

Indexed as

Antineoplastic AgentsApoptosisCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorEnzyme InhibitorsGlutathione PeroxidaseGlutathione Peroxidase GPX1Heterocyclic CompoundsHumansMembrane Potential, MitochondrialMolecular StructureOxidative StressStructure-Activity RelationshipSulfidesAntineoplastic AgentsEnzyme InhibitorsGlutathione PeroxidaseGlutathione Peroxidase GPX1GPX1 protein, humanHeterocyclic CompoundsSulfidesapoptosiscancer cellscytotoxicityDNA fragmentationglutathione peroxidaseoxidative stresspentathiepin

Identifiers

PMID32311219
PMCPMC7496275
OpenAlexW3017066062

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.