Evidence map›Paper›PMID 37349300›Full record

ArticleNature communications2023

Non-covalent inhibitors of thioredoxin glutathione reductase with schistosomicidal activity in vivo.

Valentina Z Petukhova, Sammy Y Aboagye, Matteo Ardini, Rachel P Lullo, Francesca Fata, Margaret E Byrne, Federica Gabriele, Lucy M Martin, Luke N M Harding, Vamshikrishna Gone and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
11.9field-weighted citation impact, top 1% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Endothelial c-IAP2 loss amplifies P2X7 receptor-driven inflammation and worsens schistosomiasis-associated pulmonary hypertension.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  16. Assigning function to active site residues ofFrontiers in molecular biosciences · 2023
    Article
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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

21 authors at 5 institutions in 3 countries.

Valentina Z Petukhova *Department of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Sammy Y Aboagye *Department of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, IL, USA.ORCID 0000-0001-7702-982X
Matteo Ardini *Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Rachel P LulloDepartment of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, IL, USA.ORCID 0000-0001-9002-9453
Francesca FataDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.ORCID 0000-0002-8412-6326
Margaret E ByrneDepartment of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, IL, USA.
Federica GabrieleDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Lucy M MartinDepartment of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, IL, USA.ORCID 0000-0003-3948-0913
Luke N M HardingDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0002-2079-4851
Vamshikrishna GoneUICentre, Department of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0002-8665-8465
Bikash DangiDepartment of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Daniel D LantvitUICentre, Department of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Dejan NikolicDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Rodolfo IppolitiDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Grégory EffantinUniversity of Grenoble Alpes, CEA, CNRS, IBS, F-38000, Grenoble, France.ORCID 0000-0002-6957-0875
Wai Li LingUniversity of Grenoble Alpes, CEA, CNRS, IBS, F-38000, Grenoble, France.ORCID 0000-0002-4264-5750
Jeremy J JohnsonDepartment of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Gregory R J ThatcherDepartment of Pharmacology & Toxicology, R. Ken Coit College of Pharmacy, University of Arizona, Tucson, AZ, USA.
Francesco AngelucciDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy. francesco.angelucci@univaq.it.ORCID 0000-0001-7305-7903
David L WilliamsDepartment of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, IL, USA. david_williams@rush.edu.ORCID 0000-0002-6815-4909
Pavel A PetukhovDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA. pap4@uic.edu.ORCID 0000-0003-1554-242X
University of Illinois Chicago · USRush University Medical Center · USUniversity of L'Aquila · ITCentre National de la Recherche Scientifique · FRUniversity of Arizona · US

Funding

Identification of preclinical drug candidates for the treatment of schistosomiasisR33AI127635 · NIAID · RUSH UNIVERSITY MEDICAL CENTER · PI PETUKHOV, PAVEL A, THATCHER, GREGORY R. J · 2019 to 2021
$1.3M
NIAID NIH HHS R33 AI127635
6 · The paper itself

Abstract

Only praziquantel is available for treating schistosomiasis, a disease affecting more than 200 million people. Praziquantel-resistant worms have been selected for in the lab and low cure rates from mass drug administration programs suggest that resistance is evolving in the field. Thioredoxin glutathione reductase (TGR) is essential for schistosome survival and a validated drug target. TGR inhibitors identified to date are irreversible and/or covalent inhibitors with unacceptable off-target effects. In this work, we identify noncovalent TGR inhibitors with efficacy against schistosome infections in mice, meeting the criteria for lead progression indicated by WHO. Comparisons with previous in vivo studies with praziquantel suggests that these inhibitors outperform the drug of choice for schistosomiasis against juvenile worms.

Indexed as

SchistosomiasisSchistosomicidesAnimalsMiceMultienzyme ComplexesNADH, NADPH OxidoreductasesPraziquantelSchistosomaSchistosoma mansoniMultienzyme ComplexesNADH, NADPH OxidoreductasesPraziquantelSchistosomicidesthioredoxin glutathione reductase

Identifiers

PMID37349300
PMCPMC10287695
OpenAlexW4381687213

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.