Evidence map›Paper›PMID 29885490›Full record

ArticleVirology2018

Papillomavirus E2 protein is regulated by specific fibroblast growth factor receptors.

Marsha DeSmet, Sriramana Kanginakudru, Leny Jose, Fang Xie, Timra Gilson, Elliot J Androphy

Open access · greenAbstract read
In one paragraph

Article in Virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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 3 countries.

Marsha DeSmetDepartment of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA.
Sriramana KanginakudruDepartment of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA.
Leny JoseDepartment of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA.
Fang XieDepartment of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Dermatology, Chinese People's Liberation Army General Hospital, Beijing, China.
Timra GilsonDepartment of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA.
Elliot J AndrophyDepartment of Dermatology, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: eandro@iu.edu.
Indiana University School of MedicineChinese General Hospital College of Nursing and Liberal Arts · PH

Funding

Immunology and Infectious Diseases Training ProgramT32AI060519 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI MARK H KAPLAN · 2004 to 2026
$6.0M
CONTROL OF PAPILLOMAVIRUS EXPRESSION AND TRANSFORMATIONR01CA058376 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ANDROPHY, ELLIOT J. · 1993 to 2019
$5.7M
Training in STIs and infections of global health significanceT32AI007637 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WOOLS-KALOUSTIAN, KARA KAY · 2001 to 2020
$3.4M
The Indiana Cutaneous Biological Research Training ProgramT32AR062495 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ANDROPHY, ELLIOT J. · 2013 to 2017
$649k
NCI NIH HHS R01 CA058376NIAID NIH HHS T32 AI007637NIAID NIH HHS T32 AI060519NIAMS NIH HHS T32 AR062495
6 · The paper itself

Abstract

The papillomavirus (PV) E2 protein activates transcription and replication by recruiting cellular proteins and the E1 DNA helicase to their binding sites in the viral genome. We recently demonstrated that phosphorylation of tyrosine 102 in the bovine papillomavirus (BPV-1) E2 protein restricts these activities and that fibroblast growth factor receptor-3 (FGFR3) tyrosine kinase binds PV E2. Expression of FGFR3 decreased viral replication with both wild-type and the phenylalanine substitution at position 102, inferring that another kinase targets Y102. Here we tested FGFR- 1, -2 and -4 for association with PV E2 proteins. FGFR2 but not FGFR1 or FGFR4 co-immunoprecipitated with BPV-1 E2. We found that FGFR2 suppressed replication but did not depend on phosphorylation of BPV-1 Y102. HPV-16 and -31 E2 interacted with FGFR1, -2, and -4. These results imply that the expression and activity of FGF receptors in epithelial cells can regulate the function of E2 in viral replication.

Indexed as

Host Microbial InteractionsDNA-Binding ProteinsDNA ReplicationHEK293 CellsHuman papillomavirus 16HumansImmunoprecipitationPhosphorylationProtein-Tyrosine KinasesReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 3Receptor, Fibroblast Growth Factor, Type 4Viral ProteinsVirus ReplicationDNA-Binding ProteinsE2 protein, Bovine papillomavirusFGFR1 protein, humanFGFR2 protein, humanFGFR3 protein, humanFGFR4 protein, humanProtein-Tyrosine KinasesReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 3Receptor, Fibroblast Growth Factor, Type 4Viral ProteinsFibroblast growth factor receptorPapillomavirus E2 phosphorylationViral replication

Identifiers

PMID29885490
PMCPMC6538939
OpenAlexW2805060862

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.