Evidence map›Paper›PMID 33170317›Full record

ReviewLung2020

ACE2: The Major Cell Entry Receptor for SARS-CoV-2.

Filippo Scialo, Aurora Daniele, Felice Amato, Lucio Pastore, Maria Gabriella Matera, Mario Cazzola, Giuseppe Castaldo, Andrea Bianco

Registry-linked trialAbstract readReview
In one paragraph

Review in Lung, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05165992 (Nebulized Fentanyl for Respiratory Symptoms in Patients With COVID-19), which is not on this map. Cited by 298 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
298citing papers in PubMed, 4 pooled it
–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.

NCT05165992 phase3unknown statusnot on this mapstarted 2022, after this paper: background citation

Nebulized Fentanyl for Respiratory Symptoms in Patients With COVID-19 (Ventanyl Trial)

TypeinterventionalSponsorHamad Medical CorporationRan2022 to 2022Enrolled200ConditionsCOVID-19 PneumoniaArmsNebulized Fentanyl
3 · Its place in the literature

Who cites it

298 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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238 more citing papers are in PubMed but not listed here.

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

8 authors.

Filippo ScialoDipartimento di Scienze Mediche Traslazionali, University of Campania "L. Vanvitelli", Naples, Italy.
Aurora DanieleDipartimento di Scienze e Tecnologie Ambientali Biologiche Farmaceutiche, University of Campania "L. Vanvitelli", Naples, Italy.
Felice AmatoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università Di Napoli Federico II, Naples, Italy.
Lucio PastoreDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università Di Napoli Federico II, Naples, Italy.
Maria Gabriella MateraDipartimento di Medicina Sperimentale, University of Campania "L. Vanvitelli", Naples, Italy.
Mario CazzolaDipartimento di Medicina Sperimentale, University of Rome "Tor Vergata", Rome, Italy. mario.cazzola@uniroma2.it.ORCID http://orcid.org/0000-0003-4895-9707
Giuseppe CastaldoDipartimento di Medicina Molecolare e Biotecnologie Mediche, Università Di Napoli Federico II, Naples, Italy.
Andrea BiancoDipartimento di Scienze Mediche Traslazionali, University of Campania "L. Vanvitelli", Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the unprecedented effort of the scientific community, the novel SARS-CoV-2 virus has infected more than 46 million people worldwide, killing over one million two hundred thousand. Understanding the mechanisms by which some individuals are more susceptible to SARS-CoV-2 infection and why a subgroup of them are prone to experience severe pneumonia, and death should lead to a better approach and more effective treatments for COVID-19. Here, we focus our attention on ACE2, a primary receptor of SARS-CoV-2. We will discuss its biology, tissue expression, and post-translational regulation that determine its potential to be employed by SARS-CoV-2 for cell entry. Particular attention will be given to how the ACE2 soluble form can have a great impact on disease progression and thus be used in a potential therapeutic strategy. Furthermore, we will discuss repercussions that SARS-CoV-2/ACE2 binding has on the renin-angiotensin system and beyond. Indeed, although mostly neglected, ACE2 can also act on [des-Arg 937]-bradykinin of the kinin-kallikrein system regulating coagulation and inflammation. Thorough comprehension of the role that ACE2 plays in different pathways will be the key to assess the impact that SARS-CoV-2/ACE2 binding has on organismal physiology and will help us to find better therapies and diagnostic tools.

Indexed as

Angiotensin-Converting Enzyme 2COVID-19HumansReceptors, CoronavirusRenin-Angiotensin SystemSARS-CoV-2Virus InternalizationAngiotensin-Converting Enzyme 2Receptors, CoronavirusACE2 receptorCOVID-19SARS-CoV-2

Identifiers

PMID33170317
PMCPMC7653219

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.