Evidence map›Paper›PMID 40675861›Full record

ReviewTrends in parasitology2025

Outlining the structure of cAMP compartments in Trypanosoma cruzi.

Noelia Lander

Abstract readReview
In one paragraph

Review in Trends in parasitology, 2025. 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. Article
  2. 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

1 author.

Noelia LanderDepartment of Biological Sciences, University of Cincinnati, Cincinnati, OH 45221-006, USA. Electronic address: landernm@ucmail.uc.edu.

Funding

Large-scale CRISPR screening of essential calcium-related genes in the human parasite Tr. cruziR00AI137322 · NIAID · UNIVERSITY OF CINCINNATI · PI LANDER, NOELIA · 2021 to 2022
$498k
Characterization of cAMP signaling microdomains in the human pathogen Trypanosoma cruziR21AI182544 · NIAID · UNIVERSITY OF CINCINNATI · PI LANDER, NOELIA · 2025 to 2025
$445k
NIAID NIH HHS R00 AI137322NIAID NIH HHS R21 AI182544
6 · The paper itself

Abstract

Trypanosomatids are protozoan parasites that cause deadly infectious diseases. Despite the unique characteristics of their cAMP signaling pathways, little is known about the mechanisms driving signal specificity in these early divergent eukaryotes. From the activation of adenylate cyclases in response to environmental cues to the downstream regulation of gene expression, the signaling mechanisms triggering developmental transformations in trypanosomes are poorly understood. In this review we integrate previous and new evidence supporting the existence of membrane microdomains that assemble cAMP signaling proteins in different subcellular compartments of Trypanosoma cruzi, the etiologic agent of Chagas disease. We also discuss the main cellular processes regulated by cAMP compartments in this parasite. Advances in this field are crucial to identifying new targets for antiparasitic interventions.

Indexed as

Cyclic AMPTrypanosoma cruziAdenylyl CyclasesAnimalsChagas DiseaseHumansMembrane MicrodomainsProtozoan ProteinsSignal TransductionAdenylyl CyclasesCyclic AMPProtozoan Proteinscontractile vacuole complexenvironmental sensingflagellar distal domainmetacyclogenesisosmoregulationsignaling microdomains

Identifiers

PMID40675861
PMCPMC12981958

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Registered trials

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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.