Evidence map›Paper›PMID 19036808›Full record

ArticleThe American journal of pathology2009

DEK proto-oncogene expression interferes with the normal epithelial differentiation program.

Trisha M Wise-Draper, Richard J Morreale, Teresa A Morris, Rachael A Mintz-Cole, Elizabeth E Hoskins, Scott J Balsitis, Nader Husseinzadeh, David P Witte, Kathryn A Wikenheiser-Brokamp, Paul F Lambert and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

43 citing papers in PubMed, 75 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

11 authors at 5 institutions in 1 country.

Trisha M Wise-DraperDivision of Pediatric Hematology/Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA.
Richard J Morreale
Teresa A Morris
Rachael A Mintz-Cole
Elizabeth E Hoskins
Scott J Balsitis
Nader Husseinzadeh
David P Witte
Kathryn A Wikenheiser-Brokamp
Paul F Lambert
Susanne I Wells
University of Cincinnati · USCincinnati Children's Hospital Medical Center · USUniversity of California, Berkeley · USUniversity of Cincinnati Medical Center · USUniversity of Wisconsin–Madison · US

Funding

Visualizing EBV and HCMV DNA Dynamics During InfectionP01CA022443 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI WILLIAM M. SUGDEN · 1985 to 2026
$53.1M
Functional Analysis of the HPV-16 E6 and E7 OncogenesR01CA098428 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI LAMBERT, PAUL F. · 2003 to 2012
$3.7M
Role of Rb Family in Lung Epithelial Response to InjuryR01HL079193 · NHLBI · UNIVERSITY OF CINCINNATI · PI WIKENHEISER-BROKAMP, KATHRYN ANN · 2005 to 2013
$3.4M
Role and Regulaton of the Human DEK Proto-OncogeneR01CA116316 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI WELLS, SUSANNE I · 2006 to 2016
$2.9M
Papillomavirus Proteins Mediating Cancer and SenescenceR01CA102357 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI WELLS, SUSANNE I · 2004 to 2013
$2.6M
REGULATION OF CELLULAR GROWTH AND DIFFERENTIATIONT32CA059268 · NCI · UNIVERSITY OF CINCINNATI · PI KHAN, SOHAIB A. · 1993 to 2010
$2.3M
NCI NIH HHS CA098428NCI NIH HHS CA102357NCI NIH HHS CA116316NCI NIH HHS P01 CA022443NCI NIH HHS R01 CA098428NCI NIH HHS R01 CA102357NCI NIH HHS R01 CA116316NCI NIH HHS T32 CA059268NCI NIH HHS T32 CA59268NHLBI NIH HHS HL079193NHLBI NIH HHS R01 HL079193
6 · The paper itself

Abstract

Overexpression of the DEK gene is associated with multiple human cancers, but its specific roles as a putative oncogene are not well defined. DEK transcription was previously shown to be induced by the high-risk human papillomavirus (HPV) E7 oncogene via E2F and Rb pathways. Transient DEK overexpression was able to inhibit both senescence and apoptosis in cultured cells. In at least the latter case, this mechanism involved the destabilization of p53 and the decreased expression of p53 target genes. We show here that DEK overexpression disrupts the normal differentiation program in a manner that is independent of either p53 or cell death. DEK expression was distinctly repressed upon the differentiation of cultured primary human keratinocytes, and stable DEK overexpression caused epidermal thickening in an organotypic raft model system. The observed hyperplasia involved a delay in keratinocyte differentiation toward a more undifferentiated state, and expansion of the basal cell compartment was due to increased proliferation, but not apoptosis. These phenotypes were accompanied by elevated p63 expression in the absence of p53 destabilization. In further support of bona fide oncogenic DEK activities, we report here up-regulated DEK protein levels in both human papilloma virus-positive hyperplastic murine skin and a subset of human squamous cell carcinomas. We suggest that DEK up-regulation may contribute to carcinoma development at least in part through increased proliferation and retardation of differentiation.

Indexed as

AnimalsBlotting, WesternCarcinoma, Squamous CellCell DifferentiationCell ProliferationCells, CulturedCell Transformation, NeoplasticChromosomal Proteins, Non-HistoneDNA-Binding ProteinsEpithelial CellsEpitheliumFluorescent Antibody TechniqueForeskinGene ExpressionHumansHyperplasiaChromosomal Proteins, Non-HistoneCKAP4 protein, humanDEK protein, humanDNA-Binding ProteinsMAS1 protein, humanMembrane ProteinsOncogene ProteinsPapillomavirus E7 ProteinsPDRG1 protein, humanPoly-ADP-Ribose Binding ProteinsProto-Oncogene Mas

Identifiers

PMID19036808
PMCPMC2631320
OpenAlexW2066062179

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.