Evidence map›Paper›PMID 32123072›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Cell-penetrating peptide inhibits retromer-mediated human papillomavirus trafficking during virus entry.

Pengwei Zhang, Ruben Moreno, Paul F Lambert, Daniel DiMaio

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2025
    Article
  2. Review
  3. Article
  4. Review
  5. HPV Infections-Classification, Pathogenesis, and Potential New Therapies.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Biological Membrane-Penetrating Peptides: Computational Prediction and Applications.Frontiers in cellular and infection microbiology · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Targeting Endosomal Recycling Pathways by Bacterial and Viral Pathogens.Frontiers in cell and developmental biology · 2021
    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

4 authors at 3 institutions in 1 country.

Pengwei ZhangDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520-8005.
Ruben MorenoMcArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine, Madison, WI 53705-2275.
Paul F LambertMcArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine, Madison, WI 53705-2275.
Daniel DiMaioDepartment of Genetics, Yale School of Medicine, New Haven, CT 06520-8005; daniel.dimaio@yale.edu.ORCID 0000-0002-2060-5977
University of Wisconsin–Madison · USYale Cancer Center · USYale University · US

Funding

Visualizing EBV and HCMV DNA Dynamics During InfectionP01CA022443 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Paul F. Lambert · 1985 to 2026
$53.1M
CELL TRANSFORMATION BY BOVINE PAPILLOMAVIRUSR01CA037157 · NCI · YALE UNIVERSITY · PI DIMAIO, DANIEL C. · 1985 to 2019
$9.9M
Defining Drivers of HPV-associated CarcinogenesisR35CA210807 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Paul F. Lambert · 2017 to 2026
$9.2M
Mechanisms of human papillomavirus entryR35CA242462 · NCI · YALE UNIVERSITY · PI Daniel C. Dimaio · 2020 to 2026
$6.9M
Virology Training ProgramT32AI078985 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI LAMBERT, PAUL F. · 2009 to 2018
$3.3M
Role of Retromer-mediated Retrograde Transport in HPV EntryR01AI102876 · NIAID · YALE UNIVERSITY · PI DIMAIO, DANIEL C. · 2013 to 2020
$3.1M
NCI NIH HHS P01 CA022443NCI NIH HHS R01 CA037157NCI NIH HHS R35 CA210807NCI NIH HHS R35 CA242462NIAID NIH HHS R01 AI102876NIAID NIH HHS T32 AI078985
6 · The paper itself

Abstract

Virus replication requires critical interactions between viral proteins and cellular proteins that mediate many aspects of infection, including the transport of viral genomes to the site of replication. In human papillomavirus (HPV) infection, the cellular protein complex known as retromer binds to the L2 capsid protein and sorts incoming virions into the retrograde transport pathway for trafficking to the nucleus. Here, we show that short synthetic peptides containing the HPV16 L2 retromer-binding site and a cell-penetrating sequence enter cells, sequester retromer from the incoming HPV pseudovirus, and inhibit HPV exit from the endosome, resulting in loss of viral components from cells and in a profound, dose-dependent block to infection. The peptide also inhibits cervicovaginal HPV16 pseudovirus infection in a mouse model. These results confirm the retromer-mediated model of retrograde HPV entry and validate intracellular virus trafficking as an antiviral target. More generally, inhibiting virus replication with agents that can enter cells and disrupt essential protein-protein interactions may be applicable in broad outline to many viruses.

Indexed as

AnimalsCapsid ProteinsCell-Penetrating PeptidesCervix UteriDisease Models, AnimalFemaleHEK293 CellsHeLa CellsHuman papillomavirus 16HumansMiceOncogene Proteins, ViralPapillomavirus InfectionsProtein BindingProtein Interaction MapsVaginaCapsid ProteinsCell-Penetrating PeptidesL2 protein, Human papillomavirus type 16Oncogene Proteins, Viralantiviral agentHPVprotein transduction domainretrograderetromer

Identifiers

PMID32123072
PMCPMC7084110
OpenAlexW3009758871

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.