Evidence map›Paper›PMID 32587806›Full record

ArticlePeerJ2020

A potential role for Galectin-3 inhibitors in the treatment of COVID-19.

John L Caniglia, Maheedhara R Guda, Swapna Asuthkar, Andrew J Tsung, Kiran K Velpula

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Novel inflammatory biomarkers in the prognosis of COVID-19.Therapeutic advances in respiratory disease
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Host Glycan-Lectin Interplay in SARS-CoV-2 Infection.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Article
  8. Targeting Fibrosis: From Molecular Mechanisms to Advanced Therapies.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
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  10. Review
  11. Review
  12. Article
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  18. Article
  19. Modulation of CaHandbook of experimental pharmacology · 2023
    Article
  20. 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

5 authors at 1 institution in 1 country.

John L CanigliaDepartment of Cancer Biology and Pharmacology, Neurosurgery, and Pediatrics, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Maheedhara R GudaDepartment of Cancer Biology and Pharmacology, Neurosurgery, and Pediatrics, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Swapna AsuthkarDepartment of Cancer Biology and Pharmacology, Neurosurgery, and Pediatrics, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.ORCID 0000-0002-0659-3068
Andrew J TsungDepartments of Cancer Biology and Pharmacology, Neurosurgery, and Pediatrics, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Kiran K VelpulaDepartments of Cancer Biology and Pharmacology, Pediatrics, Neurosurgery, and Pediatrics, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.ORCID 0000-0001-8947-5958
University of Illinois Urbana-Champaign · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV2), the causative agent of coronavirus disease 2019 (COVID-19), has been declared a global pandemic by the World Health Organization. With no standard of care for the treatment of COVID-19, there is an urgent need to identify therapies that may be effective in treatment. Recent evidence has implicated the development of cytokine release syndrome as the major cause of fatality in COVID-19 patients, with elevated levels of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α) observed in patients. Galectin-3 (Gal-3) is an animal lectin that has been implicated in the disease process of a variety of inflammatory conditions. Inhibitors of the small molecule Gal-3 have been shown to reduce the levels of both IL-6 and TNF-α in vitro and have shown anti-inflammatory effects in vivo. Additionally, a key domain in the spike protein of β-coronaviridae, a genus which includes SARS-CoV2, is nearly identical in morphology to human Gal-3. These spike proteins are critical for the virus' entry into host cells. Here we provide a systematic review of the available literature and an impetus for further research on the use of Gal-3 inhibitors in the treatment of COVID-19. Further, we propose a dual mechanism by which Gal-3 inhibition may be beneficial in the treatment of COVID-19, both suppressing the host inflammatory response and impeding viral attachment to host cells.

Indexed as

COVID-19CytokinesGalectin-3

Identifiers

PMID32587806
PMCPMC7301894
OpenAlexW3034947721

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.