Evidence map›Paper›PMID 35367865›Full record

ArticleBiochemical and biophysical research communications2022

Evidence for investigating GSK-3 inhibitors as potential therapeutics for severe COVID-19.

Davoud Ghazanfari, Maria Cecilia Courreges, Lydia Belinski, Stephen C Bergmeier, Kelly D McCall, Douglas J Goetz

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 1 institution in 1 country.

Davoud GhazanfariDepartment of Chemical and Biomolecular Engineering, Ohio University, Athens, OH, 45701, United States.
Maria Cecilia CourregesDepartment of Specialty Medicine, Ohio University, Athens, OH, 45701, United States.
Lydia BelinskiDepartment of Chemical and Biomolecular Engineering, Ohio University, Athens, OH, 45701, United States.
Stephen C BergmeierBiomedical Engineering Program, Ohio University, Athens, OH, 45701, United States; Department of Chemistry and Biochemistry, Ohio University, Athens, OH, 45701, United States.
Kelly D McCallDepartment of Specialty Medicine, Ohio University, Athens, OH, 45701, United States; Biomedical Engineering Program, Ohio University, Athens, OH, 45701, United States; The Diabetes Institute, Ohio University, Athens, OH, 45701, United States.
Douglas J GoetzDepartment of Chemical and Biomolecular Engineering, Ohio University, Athens, OH, 45701, United States; Biomedical Engineering Program, Ohio University, Athens, OH, 45701, United States. Electronic address: goetzd@ohio.edu.
Ohio University · US

Funding

Novel Glycogen Synthase Kinase-3 (GSK-3) Inhibitors as Therapeutic AgentsR15GM110602 · NIGMS · OHIO UNIVERSITY ATHENS · PI GOETZ, DOUGLAS J · 2016 to 2025
$1.5M
NIGMS NIH HHS R15 GM110602
6 · The paper itself

Abstract

A key component of severe COVID-19 is a "cytokine storm" i.e., the excessive expression of unneeded cytokines. Previous studies suggest that SARS-CoV-2 proteins can induce macrophages to secrete pro-inflammatory cytokines; a process that may involve Toll-like receptors (TLRs). Glycogen synthase kinase-3 (GSK-3) has been implicated in TLR signal transduction and a selective GSK-3 inhibitor, termed COB-187, dramatically attenuates cytokine expression induced by the TLR ligand lipopolysaccharide (LPS). In the present study, we provide evidence that the SARS-CoV-2 spike protein (S) and the S2 subunit (S2) induce production of CXCL10 (a chemokine elevated in severe COVID-19) by a human macrophage cell line. Further, we report that two clinically relevant GSK-3 inhibitors and COB-187 attenuate S and S2 protein-induced CXCL10 production. Combined, our observations provide impetus for investigating GSK-3 inhibitors as potential therapeutics for severe COVID-19.

Indexed as

COVID-19 Drug TreatmentGlycogen Synthase Kinase 3CytokinesHumansSARS-CoV-2Spike Glycoprotein, CoronavirusCytokinesGlycogen Synthase Kinase 3Spike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19CXCL10Cytokine stormGlycogen synthase kinase-3Spike protein

Identifiers

PMID35367865
PMCPMC8924054
OpenAlexW4221065328

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.