Evidence map›Paper›PMID 38672424›Full record

ReviewBiomolecules2024

Unmasking the Mechanism behind Miltefosine: Revealing the Disruption of Intracellular Ca

Gustavo Benaim, Alberto Paniz-Mondolfi

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2024. 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
8.7field-weighted citation impact, top 2% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Treatment ofMicroorganisms · 2025
    Review
  9. Review
  10. ComparativeFrontiers in pharmacology · 2025
    Article
  11. Review
  12. Review
  13. 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

2 authors at 2 institutions in 2 countries.

Gustavo BenaimUnidad de Señalización Celular y Bioquímica de Parásitos, Instituto de Estudios Avanzados (IDEA), Caracas 1080, Venezuela.ORCID 0000-0002-9359-5546
Alberto Paniz-MondolfiDepartment of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, Division of Microbiology, New York, NY 10029, USA.ORCID 0000-0003-1259-1736
Icahn School of Medicine at Mount Sinai · USInstituto de Estudios Avanzados · VE

Funding

Consejo Nacional de Investigaciones Cientificas y Tecnologicas (FONACIT) Grant no. 2023PGP99 to G.B.
6 · The paper itself

Abstract

Originally developed as a chemotherapeutic agent, miltefosine (hexadecylphosphocholine) is an inhibitor of phosphatidylcholine synthesis with proven antiparasitic effects. It is the only oral drug approved for the treatment of Leishmaniasis and American Trypanosomiasis (Chagas disease). Although its precise mechanisms are not yet fully understood, miltefosine exhibits broad-spectrum anti-parasitic effects primarily by disrupting the intracellular Ca

Indexed as

CalciumChagas DiseaseHomeostasisLeishmaniasisPhosphorylcholineAnimalsAntiprotozoal AgentsHumansLeishmaniaMitochondriaTrypanosoma cruziAntiprotozoal AgentsCalciummiltefosinePhosphorylcholineacidocalcisomeCa2+ channelCa2+ regulationCa2+ signalingmiltefosinemitochondriasphingosine

Identifiers

PMID38672424
PMCPMC11047903
OpenAlexW4393217002

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.