Evidence map›Paper›PMID 25516839›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2014

Serum albumin and α-1 acid glycoprotein impede the killing of Schistosoma mansoni by the tyrosine kinase inhibitor Imatinib.

Svenja Beckmann, Thavy Long, Christina Scheld, Rudolf Geyer, Conor R Caffrey, Christoph G Grevelding

Open access · goldAbstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
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  4. Chemical modulation ofWellcome open research · 2023
    Article
  5. Article
  6. Protein Kinases: Potential Drug Targets AgainstFrontiers in cellular and infection microbiology · 2021
    Review
  7. Article
  8. Targeting Kinases inFrontiers in veterinary science · 2020
    Article
  9. Article
  10. Article
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  12. Article
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  14. Article
  15. Article
  16. Taurine drinking ameliorates hepatic granuloma and fibrosis in mice infected with Schistosoma japonicum.International journal for parasitology. Drugs and drug resistance · 2016
    Article
  17. Article
  18. Article
  19. 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

6 authors at 3 institutions in 2 countries.

Svenja BeckmannBFS, Institute for Parasitology, Justus-Liebig-University, Giessen, Germany.
Thavy LongCenter for Discovery and Innovation in Parasitic Diseases and the Department of Pathology, University of California San Francisco, San Francisco, CA, USA.
Christina ScheldBFS, Institute for Parasitology, Justus-Liebig-University, Giessen, Germany.
Rudolf GeyerInstitute for Biochemistry, Justus-Liebig-University, Giessen, Germany.
Conor R CaffreyCenter for Discovery and Innovation in Parasitic Diseases and the Department of Pathology, University of California San Francisco, San Francisco, CA, USA.
Christoph G GreveldingBFS, Institute for Parasitology, Justus-Liebig-University, Giessen, Germany.
University of Giessen · DECenter for Discovery · USUniversity of California, San Francisco · US

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
Exploring statins as a small molecule therapy for treatment of schistosomiasisR21AI107390 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ARKIN, MICHELLE · 2013 to 2014
$421k
NIAID NIH HHS R21 AI107390NIDDK NIH HHS P30 DK026743
6 · The paper itself

Abstract

In the search for new drugs and drug targets to treat the flatworm disease schistosomiasis, protein kinases (PKs) have come under particular scrutiny because of their essential roles in developmental and physiological processes in schistosome parasites. In this context the application of the anti-cancer Abl tyrosine kinase (TK) inhibitor Imatinib (Gleevec/Glivec; STI-571) to adult Schistosoma mansoni in vitro has indicated negative effects on diverse physiological processes including survival. Motivated by these in vitro findings, we performed in vivo experiments in rodent models of S. mansoni infection. Unexpectedly, Imatinib had no effect on worm burden or egg-production. We found that the blood components serum albumin (SA) and alpha-1 acid glycoprotein (AGP or orosomucoid) negated Imatinib's deleterious effects on adult S. mansoni and schistosomula (post-infective larvae) in vitro. This negative effect was partially reversed by erythromycin. AGP synthesis can increase as a consequence of inflammatory processes or infection; in addition upon infection AGP levels are 6-8 times higher in mice compared to humans. Therefore, mice and probably other rodents are poor infection models for measuring the effects of Imatinib in vivo. Accordingly, we suggest the routine evaluation of the ability of AGP and SA to block in vitro anti-schistosomal effects of small molecules like Imatinib prior to laborious and expensive animal experiments.

Indexed as

Abl tyrosine kinase (Abl)ErythromycinImatinib (Gleevec, Glivec, STI-571)In vitro cultureProtein tyrosine kinase (PTK)Schistosoma mansoniSerum albumin (SA)α-1 acidic glycoprotein (AGP)

Identifiers

PMID25516839
PMCPMC4266805
OpenAlexW2049246241

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.