Evidence map›Paper›PMID 38257739›Full record

ArticleViruses2023

Diversity in Proprotein Convertase Reactivity among Human Papillomavirus Types.

Gonzalo Izaguirre, Lam Minh Uyen Phan, Shaan Asif, Samina Alam, Craig Meyers, Lijun Rong

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. 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
0.6field-weighted citation impact, top 27% 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, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

6 authors at 2 institutions in 1 country.

Gonzalo IzaguirreDepartment of Periodontics, College of Dentistry, University of Illinois Chicago, Chicago, IL 60612, USA.ORCID 0000-0002-6648-981X
Lam Minh Uyen PhanDepartment of Periodontics, College of Dentistry, University of Illinois Chicago, Chicago, IL 60612, USA.ORCID 0000-0001-7737-3807
Shaan AsifDepartment of Periodontics, College of Dentistry, University of Illinois Chicago, Chicago, IL 60612, USA.ORCID 0009-0003-9605-5005
Samina AlamDepartments of Microbiology and Immunology, College of Medicine, Penn State University, Hershey, PA 17033, USA.
Craig MeyersDepartments of Microbiology and Immunology, College of Medicine, Penn State University, Hershey, PA 17033, USA.
Lijun RongDepartments of Microbiology and Immunology, College of Medicine, University of Illinois Chicago, Chicago, IL 60612, USA.
University of Illinois Chicago · USPennsylvania State University · US

Funding

Proteolytic Regulation of HPV InfectionR21AI151674 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI IZAGUIRRE, GONZALO · 2020 to 2021
$451k
NIAID NIH HHS R21 AI151674
6 · The paper itself

Abstract

The cleavage of viral surface proteins by furin is associated with some viruses' high virulence and infectivity. The human papillomavirus (HPV) requires the proteolytic processing of its capsid proteins for activation before entry. Variability in reactivity with furin and other proprotein convertases (PCs) among HPV types was investigated. HPV16, the most prevalent and carcinogenic HPV type, reacted with PCs with the broadest selectivity compared to other types in reactions of pseudoviral particles with the recombinant PCs, furin, PC4, PC5, PACE4, and PC7. Proteolytic preactivation was assessed using a well-established entry assay into PC-inhibited cells based on the green fluorescent protein as a reporter. The inhibition of the target cell PC activity with serpin-based PC-selective inhibitors also showed a diversity of PC selectivity among HPV types. HPV16 reacted with furin at the highest rate compared to the other types in time-dependent preactivation reactions and produced the highest entry values standardized to pseudoviral particle concentration. The predominant expression of furin in keratinocytes and the high reactivity of HPV16 with this enzyme highlight the importance of selectively targeting furin as a potential antiviral therapeutic approach.

Indexed as

Papillomavirus InfectionsProprotein ConvertasesFurinHuman papillomavirus 16Human Papillomavirus VirusesHumansFurinProprotein Convertasesantiviralsfurinhost proteaseshuman papillomavirusproprotein convertasesprotease inhibitorsvirus activationvirus infectivity

Identifiers

PMID38257739
PMCPMC10820984
OpenAlexW4390236709

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.