Evidence map›Paper›PMID 32260516›Full record

ArticleMarine drugs2020

A Novel High-Throughput Screening Platform Identifies Itaconate Derivatives from Marine

Pietro Marchese, Nipun Mahajan, Enda O'Connell, Howard Fearnhead, Maria Tuohy, Janusz Krawczyk, Olivier P Thomas, Frank Barry, Mary J Murphy

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2020. 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
1.9field-weighted citation impact, top 16% 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, 20 citations in OpenAlex.

  1. Itaconate and its derivatives in human health and diseases.Signal transduction and targeted therapy · 2026
    Review
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
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  12. Article
  13. A re-evaluation ofPersoonia · 2021
    Article
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 1 institution in 1 country.

Pietro MarcheseRegenerative Medicine Institute, School of Medicine, National University of Ireland Galway, H91TK33 Galway, Ireland.
Nipun MahajanMarine Biodiscovery, School of Chemistry and Ryan Institute, National University of Ireland Galway, H91TK33 Galway, Ireland.
Enda O'ConnellGenomics and Screening Core, National Centre for Biomedical Engineering Science, National University of Ireland Galway, H91TK33 Galway, Ireland.
Howard FearnheadPharmacology and Therapeutics, School of Medicine, National University of Ireland Galway, H91TK33 Galway, Ireland.
Maria TuohyMolecular Glycobiotechnology, School of Natural Sciences, National University of Ireland Galway, H91TK33 Galway, Ireland.ORCID 0000-0003-0004-0523
Janusz KrawczykGalway University Hospital, National University of Ireland Galway, School of Medicine, H91YR71 Galway, Ireland.
Olivier P ThomasMarine Biodiscovery, School of Chemistry and Ryan Institute, National University of Ireland Galway, H91TK33 Galway, Ireland.
Frank BarryRegenerative Medicine Institute, School of Medicine, National University of Ireland Galway, H91TK33 Galway, Ireland.
Mary J MurphyRegenerative Medicine Institute, School of Medicine, National University of Ireland Galway, H91TK33 Galway, Ireland.
Ollscoil na Gaillimhe – University of Galway · IE

Funding

Irish Research Council GOIPG/2016/1113Marine Institute PBA/MB/16/01Science Foundation Ireland 09/SRC/B1794
6 · The paper itself

Abstract

Worldwide diffused diseases such as osteoarthritis, atherosclerosis or chronic kidney disease are associated with a tissue calcification process which may involve unexpected local stem cell differentiation. Current pharmacological treatments for such musculoskeletal conditions are weakly effective, sometimes extremely expensive and often absent. The potential to develop new therapies is represented by the discovery of small molecules modulating resident progenitor cell differentiation to prevent aberrant tissue calcification. The marine environment is a rich reserve of compounds with pharmaceutical potential and many novel molecules are isolated from macro and microorganisms annually. The potential of small molecules synthetized by marine filamentous fungi to influence the osteogenic and chondrogenic differentiation of human mesenchymal stem/stromal cells (hMSCs) was investigated using a novel, high-throughput automated screening platform. Metabolites synthetized by the marine-derived fungus Penicillium antarcticum were evaluated on the platform. Itaconic acid derivatives were identified as inhibitors of calcium elaboration into the matrix of osteogenically differentiated hMSCs and also inhibited hMSC chondrogenic differentiation, highlighting their capacity to impair ectopic calcification. Bioactive small molecule discovery is critical to address ectopic tissue calcification and the use of biologically relevant assays to identify naturally occurring metabolites from marine sources represents a strategy that can contribute to this effort.

Indexed as

Cell DifferentiationCells, CulturedChondrogenesisDrug DiscoveryHigh-Throughput Screening AssaysHumansMesenchymal Stem CellsOsteogenesisPenicilliumRegenerative MedicineSmall Molecule LibrariesSuccinatesitaconic acidSmall Molecule LibrariesSuccinatesdrug discoveryhigh throughput screeningmarine fungiPenicillium antarcticumregenerative medicinestem cell

Identifiers

PMID32260516
PMCPMC7230868
OpenAlexW3014098568

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.