Evidence map›Paper›PMID 23189137›Full record

ArticlePloS one2012

Transcriptional repression of E-cadherin by human papillomavirus type 16 E6.

Zarina J D'Costa, Carol Jolly, Elliot J Androphy, Andrew Mercer, Charles M Matthews, Merilyn H Hibma

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.9field-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

44 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Alternative splicing in the genome of HPV and its regulation.Frontiers in cellular and infection microbiology · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Inhibitors of DNA Methylation.Advances in experimental medicine and biology · 2022
    Review
  11. Control ofFrontiers in cellular and infection microbiology · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Interactions and Feedbacks in E-Cadherin Transcriptional Regulation.Frontiers in cell and developmental biology · 2021
    Article
  20. 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 2 countries.

Zarina J D'CostaVirus Research Unit, Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Carol Jolly
Elliot J Androphy
Andrew Mercer
Charles M Matthews
Merilyn H Hibma
University of Otago · NZIndiana University – Purdue University Indianapolis · US

Funding

Functions of Papillomavirus E6R01CA107394 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ANDROPHY, ELLIOT J. · 2004 to 2014
$3.0M
NCI NIH HHS R01 CA107394
6 · The paper itself

Abstract

There is increasing evidence supporting DNA virus regulation of the cell adhesion and tumour suppressor protein, E-cadherin. We previously reported that loss of E-cadherin in human papillomavirus (HPV) type 16-infected epidermis is contributed to by the major viral proto-oncogene E6 and is associated with reduced Langerhans cells density, potentially regulating the immune response. The focus of this study is determining how the HPV16 E6 protein mediates E-cadherin repression. We found that the E-cadherin promoter is repressed in cells expressing E6, resulting in fewer E-cadherin transcripts. On exploring the mechanism for this, repression by increased histone deacetylase activity or by increased binding of trans-repressors to the E-cadherin promoter Epal element was discounted. In contrast, DNA methyltransferase (DNMT) activity was increased in E6 expressing cells. Upon inhibiting DNMT activity using 5-Aza-2'-deoxycytidine, E-cadherin transcription was restored in the presence of HPV16 E6. The E-cadherin promoter was not directly methylated, however a mutational analysis showed general promoter repression and reduced binding of the transactivators Sp1 and AML1 and the repressor Slug. Expression of E7 with E6 resulted in a further reduction in surface E-cadherin levels. This is the first report of HPV16 E6-mediated transcriptional repression of this adhesion molecule and tumour suppressor protein.

Indexed as

Gene Expression RegulationTranscription, GeneticCadherinsDNA MethylationDNA Modification MethylasesEnzyme ActivationHCT116 CellsHistone DeacetylasesHumansOncogene Proteins, ViralPapillomavirus E7 ProteinsPromoter Regions, GeneticProtein BindingProto-Oncogene MasRepressor ProteinsRNA, MessengerCadherinsDNA Modification MethylasesE6 protein, Human papillomavirus type 16Histone DeacetylasesMAS1 protein, humanoncogene protein E7, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsProto-Oncogene MasRepressor ProteinsRNA, MessengerTranscription Factors

Identifiers

PMID23189137
PMCPMC3506579
OpenAlexW2008847855

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.