Evidence map›Paper›PMID 29463533›Full record

ArticleAntimicrobial agents and chemotherapy2018

Complex Interplay between Sphingolipid and Sterol Metabolism Revealed by Perturbations to the Leishmania Metabolome Caused by Miltefosine.

Emily G Armitage, Amjed Q I Alqaisi, Joanna Godzien, Imanol Peña, Alison J Mbekeani, Vanesa Alonso-Herranz, Ángeles López-Gonzálvez, Julio Martín, Raquel Gabarro, Paul W Denny and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2018. 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
5.1field-weighted citation impact, top 5% 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, 46 citations in OpenAlex.

  1. Review
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  6. Evaluation of theACS infectious diseases · 2024
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  7. Review
  8. Review
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  10. Unveiling drug-tolerant and persister-like cells inFrontiers in cellular and infection microbiology · 2023
    Article
  11. Article
  12. Genome deletions to overcome the directed loss of gene function inFrontiers in cellular and infection microbiology · 2022
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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

12 authors at 4 institutions in 3 countries.

Emily G ArmitageCentre for Metabolomics and Bioanalysis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Boadilla del Monte, Madrid, Spain.
Amjed Q I AlqaisiDepartment of Biosciences, Durham University, Lower Mountjoy, Durham, United Kingdom.
Joanna GodzienCentre for Metabolomics and Bioanalysis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Boadilla del Monte, Madrid, Spain.
Imanol PeñaGSK I+D Diseases of the Developing World (DDW), Parque Tecnológico de Madrid, Tres Cantos, Madrid, Spain.
Alison J MbekeaniDepartment of Biosciences, Durham University, Lower Mountjoy, Durham, United Kingdom.
Vanesa Alonso-HerranzCentre for Metabolomics and Bioanalysis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Boadilla del Monte, Madrid, Spain.
Ángeles López-GonzálvezCentre for Metabolomics and Bioanalysis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Boadilla del Monte, Madrid, Spain.
Julio MartínGSK I+D Diseases of the Developing World (DDW), Parque Tecnológico de Madrid, Tres Cantos, Madrid, Spain.
Raquel GabarroGSK I+D Diseases of the Developing World (DDW), Parque Tecnológico de Madrid, Tres Cantos, Madrid, Spain.
Paul W DennyDepartment of Biosciences, Durham University, Lower Mountjoy, Durham, United Kingdom p.w.denny@durham.ac.uk Michael.Barrett@glasgow.ac.uk cbarbas@ceu.es.
Michael P BarrettWellcome Centre for Molecular Parasitology, Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences & Glasgow Polyomics, University of Glasgow, Glasgow, United Kingdom p.w.denny@durham.ac.uk Michael.Barrett@glasgow.ac.uk cbarbas@ceu.es.
Coral BarbasCentre for Metabolomics and Bioanalysis (CEMBIO), Facultad de Farmacia, Universidad CEU San Pablo, Campus Montepríncipe, Boadilla del Monte, Madrid, Spain p.w.denny@durham.ac.uk Michael.Barrett@glasgow.ac.uk cbarbas@ceu.es.ORCID 0000-0003-4722-491X
Universidad San Pablo CEU · ESDurham University · GBUniversity of Baghdad · IQWellcome Centre for Molecular Parasitology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M024156/1Medical Research Council MR/P027989/1Wellcome TrustWellcome Trust 104111/Z/14/Z
6 · The paper itself

Abstract

With the World Health Organization reporting over 30,000 deaths and 200,000 to 400,000 new cases annually, visceral leishmaniasis is a serious disease affecting some of the world's poorest people. As drug resistance continues to rise, there is a huge unmet need to improve treatment. Miltefosine remains one of the main treatments for leishmaniasis, yet its mode of action (MoA) is still unknown. Understanding the MoA of this drug and parasite response to treatment could help pave the way for new and more successful treatments for leishmaniasis. A novel method has been devised to study the metabolome and lipidome of

Indexed as

Antiprotozoal AgentsErgosterolHumansLeishmania donovaniLeishmania majorLeishmaniasis, VisceralMembrane LipidsMetabolomePhospholipidsPhosphorylcholineSerine C-PalmitoyltransferaseSphingolipidsSterolsAntiprotozoal AgentsErgosterolMembrane LipidsmiltefosinePhospholipidsPhosphorylcholineSerine C-PalmitoyltransferaseSphingolipidsSterolsLeishmanialipid metabolismmechanisms of actionmetabolomicsmiltefosine

Identifiers

PMID29463533
PMCPMC5923112
OpenAlexW2790926941

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.