Evidence map›Paper›PMID 17030448›Full record

ArticleVirus research2007

The tyrosine kinase inhibitor genistein blocks HIV-1 infection in primary human macrophages.

Tzanko S Stantchev, Ingrid Markovic, William G Telford, Kathleen A Clouse, Christopher C Broder

Open access · greenAbstract read
In one paragraph

Article in Virus research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 35% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Kinase Inhibitors as Underexplored Antiviral Agents.Journal of medicinal chemistry · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Host-Directed Antiviral Therapy.Clinical microbiology reviews · 2020
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Sigma receptors [σRs]: biology in normal and diseased states.Journal of receptor and signal transduction research · 2016
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

5 authors at 3 institutions in 1 country.

Tzanko S StantchevDepartment of Microbiology and Immunology, F. Edward Hébert School of Medicine, Uniformed Services University Bethesda, 4301 Jones Bridge Road, MD 20814, USA.
Ingrid Markovic
William G Telford
Kathleen A Clouse
Christopher C Broder
Center for Drug Evaluation and Research · USUniformed Services University of the Health Sciences · USNational Institutes of Health · US

Funding

HIV-1 Fusion CoreceptorsR01AI043885 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI BRODER, CHRISTOPHER C · 1998 to 2008
$1.8M
HIV-1 Fusion CoreceptorsR21AI043885 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI BRODER, CHRISTOPHER · 2003 to 2003
$299k
NIAID NIH HHS AI43885NIAID NIH HHS R01 AI043885NIAID NIH HHS R21 AI043885
6 · The paper itself

Abstract

Binding of HIV-1 envelope glycoprotein (Env) to its cellular receptors elicits a variety of signaling events, including the activation of select tyrosine kinases. To evaluate the potential role of such signaling, we examined the effects of the tyrosine kinase inhibitor, genistein, on HIV-1 entry and infection of human macrophages using a variety of assays. Without altering cell viability, cell surface expression of CD4 and CCR5 or their abilities to interact with Env, genistein inhibited infection of macrophages by reporter gene-encoding, beta-lactamase containing, or wild type virions, as well as Env-mediated cell-fusion. The observation that genistein blocked virus infection if applied before, during or immediately after the infection period, but not 24h later; coupled with a more pronounced inhibition of infection in the reporter gene assays as compared to both beta-lactamase and p24 particle entry assays, imply that genistein exerts its inhibitory effects on both entry and early post-entry steps. These findings suggest that other exploitable targets, or steps, of the HIV-1 infection process may exist and could serve as additional opportunities for the development of new therapeutics.

Indexed as

Cells, CulturedDose-Response Relationship, DrugGenisteinHIV-1HIV Envelope Protein gp120HIV InfectionsHumansMacrophagesMembrane FusionProtein-Tyrosine KinasesTime FactorsTumor Necrosis Factor-alphaVirus ReplicationGenisteinHIV Envelope Protein gp120Protein-Tyrosine KinasesTumor Necrosis Factor-alpha

Identifiers

PMID17030448
PMCPMC1847631
OpenAlexW1996938063

What OpenQuestion holds

Textmetadata
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.