Evidence map›Paper›PMID 26004537›Full record

ReviewTrends in parasitology2015

cAMP signalling in trypanosomatids: role in pathogenesis and as a drug target.

Laura Makin, Eva Gluenz

Open access · hybridAbstract readReview
In one paragraph

Review 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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Adhesion ofmSphere · 2024
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Frequent Recombination Events inPathogens (Basel, Switzerland) · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Adenylate Cyclases ofPathogens (Basel, Switzerland) · 2018
    Review
  12. 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

2 authors at 1 institution in 1 country.

Laura MakinSir William Dunn School of Pathology, University of Oxford, Oxford, UK. Electronic address: laura.makin@path.ox.ac.uk.
Eva GluenzSir William Dunn School of Pathology, University of Oxford, Oxford, UK.
University of Oxford · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Despite recent research linking cAMP signalling to virulence in trypanosomatids and detailed studies of trypanosomatid adenylyl cyclases (ACs) and phosphodiesterases (PDEs) since their discoveries 40 years ago, downstream components of the pathway and their biological functions have remained remarkably elusive. However, in recent years, significant discoveries have been made: a role for parasite ACs has been proposed in cytokinesis, evasion of the host immune response, and social motility. cAMP phosphodiesterases PDEB1 and PDEB2 were found to be essential for survival and virulence of Trypanosoma brucei and, in Trypanosoma cruzi, PDEC2 was shown to be required for normal osmoregulation. As we discuss here, these breakthroughs have led to an ongoing surge in the development of PDE inhibitors as lead compounds for trypanocidal drugs.

Indexed as

Signal TransductionAdenylyl CyclasesCyclic AMPDrug DiscoveryEuglenozoa InfectionsHost-Parasite InteractionsHumansPhosphodiesterase InhibitorsPhosphoric Diester HydrolasesTrypanocidal AgentsTrypanosomatinaAdenylyl CyclasesCyclic AMPPhosphodiesterase InhibitorsPhosphoric Diester HydrolasesTrypanocidal Agentsadenylyl cyclasescAMPdrug targetphosphodiesterasestrypanosomatids

Identifiers

PMID26004537
PMCPMC4534343
OpenAlexW1541536598

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.