Evidence map›Paper›PMID 28107750›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2017

Effect of clinically approved HDAC inhibitors on Plasmodium, Leishmania and Schistosoma parasite growth.

Ming Jang Chua, Megan S J Arnold, Weijun Xu, Julien Lancelot, Suzanne Lamotte, Gerald F Späth, Eric Prina, Raymond J Pierce, David P Fairlie, Tina S Skinner-Adams and 1 more

Abstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Characterization of the Activities of Vorinostat AgainstInternational journal of molecular sciences · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. The mitochondrion ofProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

11 authors.

Ming Jang ChuaGriffith Institute for Drug Discovery, Griffith University, Queensland, Australia.
Megan S J ArnoldGriffith Institute for Drug Discovery, Griffith University, Queensland, Australia.
Weijun XuInstitute for Molecular Bioscience, The University of Queensland, Brisbane, 4072, Australia.
Julien LancelotUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 8204- CIIL -Centre D'Infection et D'Immunité de Lille, F-59000 Lille, France.
Suzanne LamotteInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.
Gerald F SpäthInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.
Eric PrinaInstitut Pasteur and INSERM U1201, Unité de Parasitologie Moléculaire et Signalisation, Paris, France.
Raymond J PierceUniv. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 8204- CIIL -Centre D'Infection et D'Immunité de Lille, F-59000 Lille, France.
David P FairlieInstitute for Molecular Bioscience, The University of Queensland, Brisbane, 4072, Australia.
Tina S Skinner-AdamsGriffith Institute for Drug Discovery, Griffith University, Queensland, Australia.
Katherine T AndrewsGriffith Institute for Drug Discovery, Griffith University, Queensland, Australia. Electronic address: k.andrews@griffith.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria, schistosomiasis and leishmaniases are among the most prevalent tropical parasitic diseases and each requires new innovative treatments. Targeting essential parasite pathways, such as those that regulate gene expression and cell cycle progression, is a key strategy for discovering new drug leads. In this study, four clinically approved anti-cancer drugs (Vorinostat, Belinostat, Panobinostat and Romidepsin) that target histone/lysine deacetylase enzymes were examined for in vitro activity against Plasmodium knowlesi, Schistosoma mansoni, Leishmania amazonensis and L. donovani parasites and two for in vivo activity in a mouse malaria model. All four compounds were potent inhibitors of P. knowlesi malaria parasites (IC

Indexed as

AcetylationAdministration, OralAnimalsDepsipeptidesHEK293 CellsHistone Deacetylase InhibitorsHistone DeacetylasesHistonesHumansHydroxamic AcidsIndolesInhibitory Concentration 50LeishmaniaLife Cycle StagesMalariaMicebelinostatDepsipeptidesHistone Deacetylase InhibitorsHistone DeacetylasesHistonesHydroxamic AcidsIndolesPanobinostatromidepsinSulfonamidesVorinostatHistone deacetylaseLeishmaniaPanobinostatPlasmodiumSchistosoma

Identifiers

PMID28107750
PMCPMC5241585

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.