Evidence map›Paper›PMID 31916356›Full record

ArticleAngewandte Chemie (International ed. in English)2020

Functional Disruption of the Cancer-Relevant Interaction between Survivin and Histone H3 with a Guanidiniocarbonyl Pyrrole Ligand.

Cecilia Vallet, Dennis Aschmann, Christine Beuck, Matthias Killa, Annika Meiners, Marcel Mertel, Martin Ehlers, Peter Bayer, Carsten Schmuck, Michael Giese and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

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  17. NMR Spectroscopy of supramolecular chemistry on protein surfaces.Beilstein journal of organic chemistry · 2020
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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

11 authors at 1 institution in 1 country.

Cecilia ValletDepartment of Molecular Biology II, University of Duisburg-Essen, Universitätsstraße 5, 45141, Essen, Germany.ORCID 0000-0002-9413-846X
Dennis AschmannInstitute for Organic Chemistry, University of Duisburg-Essen, Germany.
Christine BeuckDepartment of Structural and Medicinal Biochemistry, University of Duisburg-Essen, Germany.
Matthias KillaInstitute for Organic Chemistry, University of Duisburg-Essen, Germany.
Annika MeinersDepartment of Molecular Biology II, University of Duisburg-Essen, Universitätsstraße 5, 45141, Essen, Germany.
Marcel MertelInstitute for Organic Chemistry, University of Duisburg-Essen, Germany.
Martin EhlersInstitute for Organic Chemistry, University of Duisburg-Essen, Germany.
Peter BayerDepartment of Structural and Medicinal Biochemistry, University of Duisburg-Essen, Germany.
Carsten SchmuckInstitute for Organic Chemistry, University of Duisburg-Essen, Germany.
Michael GieseInstitute for Organic Chemistry, University of Duisburg-Essen, Germany.
Shirley K KnauerDepartment of Molecular Biology II, University of Duisburg-Essen, Universitätsstraße 5, 45141, Essen, Germany.
University of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein Survivin is highly upregulated in most cancers and considered to be a key player in carcinogenesis. We explored a supramolecular approach to address Survivin as a drug target by inhibiting the protein-protein interaction of Survivin and its functionally relevant binding partner Histone H3. Ligand L1 is based on the guanidiniocarbonyl pyrrole cation and serves as a highly specific anion binder in order to target the interaction between Survivin and Histone H3. NMR titration confirmed binding of L1 to Survivin's Histone H3 binding site. The inhibition of the Survivin-Histone H3 interaction and consequently a reduction of cancer cell proliferation were demonstrated by microscopic and cellular assays.

Indexed as

Binding SitesCell Line, TumorCell ProliferationHistonesHumansLigandsMagnetic Resonance SpectroscopyMolecular Docking SimulationProtein BindingPyrrolesSurvivinBIRC5 protein, humanHistonesLigandsPyrrolesSurvivincancermolecular recognitionPPI inhibitorssupramolecular chemistrysurvivin

Identifiers

PMID31916356
PMCPMC7155087
OpenAlexW2999447048

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.