Evidence map›Paper›PMID 33303190›Full record

ReviewBiochemical and biophysical research communications2021

The biogenesis of SARS-CoV-2 spike glycoprotein: multiple targets for host-directed antiviral therapy.

Silvia Santopolo, Anna Riccio, M Gabriella Santoro

Abstract readReview
In one paragraph

Review in Biochemical and biophysical research communications, 2021. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
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  4. Review
  5. Review
  6. Article
  7. Article
  8. Principles of SARS-CoV-2 glycosylation.Current opinion in structural biology · 2022
    Review
  9. Human inhalable antibody fragments neutralizing SARS-CoV-2 variants for COVID-19 therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  10. Article
  11. Article
  12. ERp57/PDIA3: new insight.Cellular & molecular biology letters · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. 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

3 authors.

Silvia SantopoloDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Anna RiccioDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
M Gabriella SantoroDepartment of Biology, University of Rome Tor Vergata, Rome, Italy; Institute of Translational Pharmacology, CNR, Rome, Italy. Electronic address: santoro@uniroma2.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19 (coronavirus disease-19), represents a far more serious threat to public health than SARS and MERS coronaviruses, due to its ability to spread more efficiently than its predecessors. Currently, there is no worldwide-approved effective treatment for COVID-19, urging the scientific community to intense efforts to accelerate the discovery and development of prophylactic and therapeutic solutions against SARS-CoV-2 infection. In particular, effective antiviral drugs are urgently needed. With few exceptions, therapeutic approaches to combat viral infections have traditionally focused on targeting unique viral components or enzymes; however, it has now become evident that this strategy often fails due to the rapid emergence of drug-resistant viruses. Targeting host factors that are essential for the virus life cycle, but are dispensable for the host, has recently received increasing attention. The spike glycoprotein, a component of the viral envelope that decorates the virion surface as a distinctive crown ("corona") and is essential for SARS-CoV-2 entry into host cells, represents a key target for developing therapeutics capable of blocking virus invasion. This review highlights aspects of the SARS-CoV-2 spike biogenesis that may be amenable to host-directed antiviral targeting.

Indexed as

COVID-19 Drug TreatmentAntiviral AgentsCOVID-19GlycosylationHumansMolecular Targeted TherapyProtein FoldingSARS-CoV-2Spike Glycoprotein, CoronavirusVirus InternalizationAntiviral AgentsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2AntiviralCoronavirusCOVID-19ERp57FurinN-Glycosylation

Identifiers

PMID33303190
PMCPMC7698684

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.