Evidence map›Paper›PMID 30214075›Full record

ArticleScientific reports2018

Exploration of ligand binding modes towards the identification of compounds targeting HuR: a combined STD-NMR and Molecular Modelling approach.

Francesca Vasile, Serena Della Volpe, Francesca Alessandra Ambrosio, Giosuè Costa, M Yagiz Unver, Chiara Zucal, Daniela Rossi, Emanuela Martino, Alessandro Provenzani, Anna K H Hirsch and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  6. Neurodegeneration: can metabolites fromFrontiers in pharmacology · 2024
    Article
  7. Article
  8. Low Molecular Weight Inhibitors Targeting the RNA-Binding Protein HuR.International journal of molecular sciences · 2023
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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

13 authors at 5 institutions in 2 countries.

Francesca VasileDepartment of Chemistry, University of Milan, Via Golgi 19, 20133, Milano, Italy.ORCID 0000-0002-3926-8261
Serena Della VolpeDepartment of Chemistry, University of Milan, Via Golgi 19, 20133, Milano, Italy.
Francesca Alessandra AmbrosioDepartment of Health Sciences, University "Magna Græcia" of Catanzaro, Viale Europa, 88100, Catanzaro, Italy.
Giosuè CostaDepartment of Health Sciences, University "Magna Græcia" of Catanzaro, Viale Europa, 88100, Catanzaro, Italy.ORCID 0000-0003-0947-9479
M Yagiz UnverHelmholtz Institute for Pharmaceutical Research Saarland (HIPS) - Helmholtz Centre for Infection Research (HZI), Department of Drug Design and Optimization, Campus building E8.1, 66123, Saarbrücken, Germany.
Chiara ZucalCentre for Integrative Biology, CIBIO, University of Trento, Via Sommarive 9, 38123, Povo, TN, Italy.
Daniela RossiDepartment of Drug Sciences, Medicinal Chemistry and Technology Section, University of Pavia, Via Taramelli 12, 27100, Pavia, Italy.
Emanuela MartinoDepartment of Earth and Environmental Sciences, University of Pavia, via S. Epifanio 14, 27100, Pavia, Italy.
Alessandro ProvenzaniCentre for Integrative Biology, CIBIO, University of Trento, Via Sommarive 9, 38123, Povo, TN, Italy.
Anna K H HirschHelmholtz Institute for Pharmaceutical Research Saarland (HIPS) - Helmholtz Centre for Infection Research (HZI), Department of Drug Design and Optimization, Campus building E8.1, 66123, Saarbrücken, Germany.
Stefano AlcaroDepartment of Health Sciences, University "Magna Græcia" of Catanzaro, Viale Europa, 88100, Catanzaro, Italy.ORCID 0000-0002-0437-358X
Donatella PotenzaDepartment of Chemistry, University of Milan, Via Golgi 19, 20133, Milano, Italy.
Simona CollinaDepartment of Drug Sciences, Medicinal Chemistry and Technology Section, University of Pavia, Via Taramelli 12, 27100, Pavia, Italy. simona.collina@unipv.it.ORCID 0000-0002-2954-7558
Magna Graecia University · ITUniversity of Milan · ITUniversity of Pavia · ITHelmholtz Centre for Infection Research · DEUniversity of Trento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Post-transcriptional processes have been recognised as pivotal in the control of gene expression, and impairments in RNA processing are reported in several pathologies (i.e., cancer and neurodegeneration). Focusing on RNA-binding proteins (RBPs), the involvement of Embryonic Lethal Abnormal Vision (ELAV) or Hu proteins and their complexes with target mRNAs in the aetiology of various dysfunctions, has suggested the great potential of compounds able to interfere with the complex stability as an innovative pharmacological strategy for the treatment of numerous diseases. Here, we present a rational follow-up investigation of the interaction between ELAV isoform HuR and structurally-related compounds (i.e., flavonoids and coumarins), naturally decorated with different functional groups, by means of STD-NMR and Molecular Modelling. Our results represent the foundation for the development of potent and selective ligands able to interfere with ELAV-RNA complexes.

Indexed as

CoumarinsELAV-Like Protein 1FlavonoidsGene Expression RegulationHumansLigandsMagnetic Resonance ImagingModels, MolecularMolecular Docking SimulationMolecular Dynamics SimulationRNA, MessengerRNA Processing, Post-TranscriptionalCoumarinsELAVL1 protein, humanELAV-Like Protein 1FlavonoidsLigandsRNA, Messenger

Identifiers

PMID30214075
PMCPMC6137155
OpenAlexW2889854651

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.