Evidence map›Paper›PMID 29624161›Full record

ArticleThe Journal of general virology2018

E5 can be expressed in anal cancer and leads to epidermal growth factor receptor-induced invasion in a human papillomavirus 16-transformed anal epithelial cell line.

Erin Isaacson Wechsler, Sharof Tugizov, Rossana Herrera, Maria Da Costa, Joel M Palefsky

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in The Journal of general virology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
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  5. Suppression of E6 Oncogene Induces Apoptosis in CaSki Cervical Cancer Cells.Asian Pacific journal of cancer prevention : APJCP · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Erin Isaacson WechslerDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Sharof TugizovDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Rossana HerreraDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Maria Da CostaDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Joel M PalefskyDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
University of California, San Francisco · US

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jennifer Leigh Clarke · 1999 to 2026
$209.7M
University of Southern CaliforniaU01CA121947 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SPARANO, JOSEPH A. · 2006 to 2014
$54.7M
Molecular mechanisms of oral HIV transmission modeling MTCTR01DE023315 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TUGIZOV, SHAROF M · 2013 to 2017
$2.3M
NCI NIH HHS P30 CA082103NCI NIH HHS U01 CA121947NIDCR NIH HHS R01 DE023315
6 · The paper itself

Abstract

We created the first human papillomavirus (HPV)-16-immortalized anal epithelial cell line, known as AKC2 cells to establish an in vitro model of HPV-16-induced anal carcinogenesis. Consistent with detection of E6, E7 and E5 expression in anal cancer biopsies, AKC2 cells expressed high levels of all three HPV oncogenes. Also, similar to findings in anal cancer biopsies, epidermal growth factor receptor (EGFR) was overexpressed in AKC2 cells. AKC2 cells exhibited a poorly differentiated and invasive phenotype in three-dimensional raft culture and inhibition of EGFR function abrogated AKC2 invasion. Reducing E5 expression using E5-targeted siRNAs in AKC2 cells led to knockdown of E5 expression, but also HPV-16 E2, E6 and E7 expression. AKC2 cells treated with E5-targeted siRNA had reduced levels of total and phosphorylated EGFR, and reduced invasion. Rescue of E6/E7 expression with simultaneous E5 knockdown confirmed that E5 plays a key role in EGFR overexpression and EGFR-induced invasion.

Indexed as

Anus NeoplasmsCarcinogenesisCell DifferentiationCell Line, TransformedEpithelial CellsErbB ReceptorsGene Knockdown TechniquesHuman papillomavirus 16HumansModels, BiologicalOncogene Proteins, ViralPapillomavirus E7 ProteinsRepressor ProteinsRNA, Small InterferingViroporin ProteinsE6 protein, Human papillomavirus type 16ErbB Receptorsoncogene protein E5, Human papillomavirus type 16oncogene protein E7, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsRepressor ProteinsRNA, Small InterferingViroporin Proteinsanal cancerepidermal growth factorHPV 16 E5HPV 16-postive anal cell lineHuman Papillomaviruses

Identifiers

PMID29624161
PMCPMC6537625
OpenAlexW2796394679

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.