Evidence map›Paper›PMID 30232605›Full record

ReviewParasitology research2018

Experimental models in Chagas disease: a review of the methodologies applied for screening compounds against Trypanosoma cruzi.

Cristina Fonseca-Berzal, Vicente J Arán, José A Escario, Alicia Gómez-Barrio

Abstract readReview
PubMed Publisher
In one paragraph

Review in Parasitology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Optimization of anBiology methods & protocols · 2026
    Article
  5. Article
  6. Reporter genes and transgenicFrontiers in medicine · 2025
    Review
  7. Article
  8. Article
  9. Murine colon organoids as a novel model to studyFrontiers in cellular and infection microbiology · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Anti-International journal of molecular sciences · 2021
    Article
  15. Optimization and biological validation of anBiology methods & protocols · 2021
    Article
  16. Dynamics of Mammalian Cell Infection byFrontiers in microbiology · 2020
    Article
  17. Hybrids ofMolecules (Basel, Switzerland) · 2019
    Article
  18. Review
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

4 authors at 2 institutions in 1 country.

Cristina Fonseca-BerzalDepartamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid, Pza. Ramón y Cajal s/n, 28040, Madrid, Spain. crfonseca@pdi.ucm.es.
Vicente J AránInstituto de Química Médica (IQM), Consejo Superior de Investigaciones Científicas (CSIC), c/ Juan de la Cierva 3, 28006, Madrid, Spain.
José A EscarioDepartamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid, Pza. Ramón y Cajal s/n, 28040, Madrid, Spain.
Alicia Gómez-BarrioDepartamento de Microbiología y Parasitología, Facultad de Farmacia, Universidad Complutense de Madrid, Pza. Ramón y Cajal s/n, 28040, Madrid, Spain.
Universidad Complutense de Madrid · ESInstituto de Química Médica · ES

Funding

Ministerio de Economía, Industria y Competitividad (MINEICO) SAF2015-66690-R
6 · The paper itself

Abstract

One of the main problems of Chagas disease (CD), the parasitic infection caused by Trypanosoma cruzi, is the lack of a completely satisfactory treatment, which is currently based on two old nitroheterocyclic drugs (i.e., nifurtimox and benznidazole) that show important limitations for treating patients. In this context, many laboratories look for alternative therapies potentially applicable to the treatment, and therefore, research in CD chemotherapy works in the design of experimental protocols for detecting molecules with activity against T. cruzi. Phenotypic assays are considered the most valuable strategy for screening these antiparasitic compounds. Among them, in vitro experiments are the first step to test potential anti-T. cruzi drugs directly on the different parasite forms (i.e., epimastigotes, trypomastigotes, and amastigotes) and to detect cytotoxicity. Once the putative trypanocidal drug has been identified in vitro, it must be moved to in vivo models of T. cruzi infection, to explore (i) acute toxicity, (ii) efficacy during the acute infection, and (iii) efficacy in the chronic disease. Moreover, in silico approaches for predicting activity have emerged as a supporting tool for drug screening procedures. Accordingly, this work reviews those in vitro, in vivo, and in silico methods that have been routinely applied during the last decades, aiming to discover trypanocidal compounds that contribute to developing more effective CD treatments.

Indexed as

AnimalsChagas DiseaseDrug Evaluation, PreclinicalHumansLife Cycle StagesMiceModels, TheoreticalNitroimidazolesParasitic Sensitivity TestsTrypanocidal AgentsTrypanosoma cruzibenzonidazoleNitroimidazolesTrypanocidal AgentsChagas diseaseExperimental chemotherapyIn silicoIn vitroIn vivoTrypanosoma cruzi

Identifiers

PMID30232605
OpenAlexW2891512704

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.