Evidence map›Paper›PMID 37864277›Full record

ReviewChemical biology & drug design2024

Glucose metabolism in the pathogenic free-living amoebae: Tempting targets for treatment development.

Jillian E Milanes, Samuel Kwain, Allyson Drawdy, Laura Dodson, Matthew T Monaghan, Christopher A Rice, Brian N Dominy, Daniel C Whitehead, James C Morris

Open access · hybridAbstract readReview
In one paragraph

Review in Chemical biology & drug design, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 2 institutions in 1 country.

Jillian E MilanesDepartment of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
Samuel KwainDepartment of Chemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0002-4065-2025
Allyson DrawdyDepartment of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
Laura DodsonDepartment of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
Matthew T MonaghanDepartment of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
Christopher A RiceDepartment of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, Indiana, USA.
Brian N DominyDepartment of Chemistry, Clemson University, Clemson, South Carolina, USA.
Daniel C WhiteheadDepartment of Chemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0001-6881-2628
James C MorrisDepartment of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
Clemson University · USPurdue University West Lafayette · US

Funding

Regulation of Cryptosporidium DevelopmentP20GM146584 · NIGMS · CLEMSON UNIVERSITY · PI KERRY Scot SMITH · 2022 to 2026
$13.5M
Enolase inhibitors as therapeutic leads for Naegleria fowleri infectionsR21AI171217 · NIAID · CLEMSON UNIVERSITY · PI MORRIS, JAMES CULVIN, MOSEMAN, E. ASHLEY · 2023 to 2024
$468k
Approaches for genetic manipulation of Naegleria fowleriR21AI175463 · NIAID · CLEMSON UNIVERSITY · PI MORRIS, JAMES CULVIN · 2023 to 2024
$419k
NIAID NIH HHS R21 AI171217NIAID NIH HHS R21 AI175463NIGMS NIH HHS P20 GM146584NIH HHS
6 · The paper itself

Abstract

Pathogenic free-living amoebae (pFLA) are single-celled eukaryotes responsible for causing intractable infections with high morbidity and mortality in humans and animals. Current therapeutic approaches include cocktails of antibiotic, antifungal, and antimicrobial compounds. Unfortunately, the efficacy of these can be limited, driving the need for the discovery of new treatments. Pan anti-amebic agents would be ideal; however, identifying these agents has been a challenge, likely due to the limited evolutionary relatedness of the different pFLA. Here, we discuss the potential of targeting amoebae glucose metabolic pathways as the differences between pFLA and humans suggest specific inhibitors could be developed as leads for new therapeutics.

Indexed as

AmoebaAnimalsAntifungal AgentsHumansAntifungal Agentsdrug discoveryglucosemetabolismpathogenic amoebaetarget-based drug design

Identifiers

PMID37864277
PMCPMC10843269
OpenAlexW4387840649

What OpenQuestion holds

Textmetadata
LicenceTDM
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.