Evidence map›Paper›PMID 25498194›Full record

ArticleTrends in parasitology2015

Targeting sterol metabolism for the development of antileishmanials.

Sébastien Pomel, Sandrine Cojean, Philippe M Loiseau

Abstract readComment
PubMed Publisher
In one paragraph

Article in Trends in parasitology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Frontiers in immunology · 2026
    Review
  2. Unravelling the myth surrounding sterol biosynthesis as plausible target for drug design against leishmaniasis.Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Sébastien PomelAntiparasitic Chemotherapy, UMR 8076 CNRS BioCIS, Labex LERMIT, University Paris-Sud, 5 rue Jean-Baptiste Clément, 92290- Châtenay-Malabry, France. Electronic address: sebastien.pomel@u-psud.fr.
Sandrine CojeanAntiparasitic Chemotherapy, UMR 8076 CNRS BioCIS, Labex LERMIT, University Paris-Sud, 5 rue Jean-Baptiste Clément, 92290- Châtenay-Malabry, France.
Philippe M LoiseauAntiparasitic Chemotherapy, UMR 8076 CNRS BioCIS, Labex LERMIT, University Paris-Sud, 5 rue Jean-Baptiste Clément, 92290- Châtenay-Malabry, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane sterol profiles differ between humans and Leishmania parasites, and the sterol pathway has been investigated for potential therapeutic targets. Recently, mutants of the C14α-sterol demethylase in Leishmania major were found to have several major alterations such as increased membrane fluidity, hypersensitivity to heat stress, and severe reduction of virulence.

Indexed as

AnimalsEukaryotaFemaleLeishmaniaSterolsSterolsantileishmanial agentsbiological targetLeishmania sp.sterol metabolism

Identifiers

What OpenQuestion holds

Textmetadata
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.