Evidence map›Paper›PMID 19272531›Full record

ArticleDifferentiation; research in biological diversity2009

Abnormal differentiation, hyperplasia and embryonic/perinatal lethality in BK5-T/t transgenic mice.

Xin Chen, Robin Schneider-Broussard, Debra Hollowell, Mark McArthur, Collene R Jeter, Fernando Benavides, John DiGiovanni, Dean G Tang

Open access · greenAbstract read
In one paragraph

Article in Differentiation; research in biological diversity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review: Experimental models for Barrett's esophagus and esophageal adenocarcinoma.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Review
  4. 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

8 authors at 1 institution in 1 country.

Xin ChenDepartment of Carcinogenesis, The University of Texas M.D. Anderson Cancer Center, Science Park-Research Division, 1808 Park Road 1-C, P.O. Box 389, Smithville, TX 78957, USA.
Robin Schneider-Broussard
Debra Hollowell
Mark McArthur
Collene R Jeter
Fernando Benavides
John DiGiovanni
Dean G Tang
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
15-Lipoxygenase 2 is a Prostate Senescence GeneR01AG023374 · NIA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TANG, DEAN G. · 2004 to 2008
$1.4M
Nucleotide Regulation of Apaf-1 Apoptosome and ApoptosisR01ES015888 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TANG, DEAN G. · 2007 to 2010
$1.3M
Genome-wide association study of cutaneous squamous cell carincomaR01CA166672 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI ASGARI, MARYAM MANDANA · 2013 to 2016
$1.3M
A Novel Mechanism to Regulate Caspase-8 Activation on the Mitochondrial MembraneR21ES015893 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TANG, DEAN G. · 2007 to 2008
$419k
NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA166672NCI NIH HHS R01 CA166672NIA NIH HHS R01 AG023374NIA NIH HHS R01-AG023374NIEHS NIH HHS ES07784NIEHS NIH HHS P30 ES007784NIEHS NIH HHS R01 ES015888NIEHS NIH HHS R01-ES015888NIEHS NIH HHS R21 ES015893
6 · The paper itself

Abstract

The cell-of-origin has a great impact on the types of tumors that develop and the stem/progenitor cells have long been considered main targets of malignant transformation. The SV40 (SV40-Simian Virus 40) large T and small t antigens (T/t), have been targeted to multiple-differentiated cellular compartments in transgenic mice. In most of these studies, transgenic animals develop tumors without apparent defects in animal development. In this study, we used the bovine keratin 5 (BK5) promoter to target the T/t antigens to stem/progenitor cell-containing cytokeratin 5 (CK5) cellular compartment. A transgene construct, BK5-T/t, was made and microinjected into the male pronucleus of FVB/N mouse oocytes. After implanting approximately 1700 embryos, only 7 transgenics were obtained, including 4 embryos (E9.5, E13, E15, and E20) and 3 postnatal animals, which died at P1, P2, and P18, respectively. Immunohistological analysis revealed aberrant differentiation and prominent hyperplasia in several transgenic CK5 tissues, especially the upper digestive organs (tongue, oral mucosa, esophagus, and forestomach) and epidermis, the latter of which also showed focal dysplasia. Altogether, these results indicate that constitutive expression of the T/t antigens in CK5 cellular compartment results in abnormal epithelial differentiation and leads to embryonic/perinatal animal lethality.

Indexed as

Cell DifferentiationHyperplasiaPromoter Regions, GeneticAnimalsAntigens, Polyomavirus TransformingApoptosisEpidermisEpithelial CellsGastrointestinal TractGene Expression RegulationKeratin-5MaleMiceMice, TransgenicSimian virus 40TongueAntigens, Polyomavirus TransformingKeratin-5

Identifiers

PMID19272531
PMCPMC2680132
OpenAlexW2137073231

What OpenQuestion 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 OpenQuestion graph.