Evidence map›Paper›PMID 10980598›Full record

ArticleOncogene2000

Constitutive expression of erbB2 in epidermis of transgenic mice results in epidermal hyperproliferation and spontaneous skin tumor development.

K Kiguchi, D Bol, S Carbajal, L Beltrán, S Moats, K Chan, J Jorcano, J DiGiovanni

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

31 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Genetically modified laboratory mice with sebaceous glands abnormalities.Cellular and molecular life sciences : CMLS · 2016
    Review
  12. Article
  13. Article
  14. Reconstructing skin cancers using animal models.Cancer metastasis reviews · 2013
    Review
  15. Asymmetric cell divisions in the epidermis.International review of cell and molecular biology · 2012
    Review
  16. Review
  17. Article
  18. Article
  19. 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

8 authors at 3 institutions in 3 countries.

K KiguchiThe University of Texas, MD Anderson Cancer Center, Department of Carcinogenesis, Science Park-Research Division, PO Box 389, Smithville, Texas, TX 78957, USA.
D Bol
S Carbajal
L Beltrán
S Moats
K Chan
J Jorcano
J DiGiovanni
The University of Texas MD Anderson Cancer Center · USBristol-Myers Squibb (Germany) · DEUniversidad Complutense de Madrid · ES

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
TYROSINE KINASES AND C SRC IN SKIN CANCERR01CA076520 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIGIOVANNI, JOHN · 1998 to 2012
$3.7M
NCI NIH HHS CA16672NCI NIH HHS CA76520NIEHS NIH HHS ES07784
6 · The paper itself

Abstract

The erbB family of receptor tyrosine kinases, which consists of the epidermal growth factor receptor (EGFr/erbB1), erbB2 (neu), erbB3 and erbB4, has been shown to be important for both normal development as well as neoplasia. The expression of rat erbB2 was targeted to the basal layer of mouse epidermis with the bovine keratin 5 promoter. Overexpression of wild type rat erbB2 in the basal layer of epidermis led to alopecia, follicular hyperplasia and sebaceous gland enlargement as well as hyperplasia of the interfollicular epidermis. Spontaneous papillomas, some of which converted to squamous cell carcinomas, arose in homozygous erbB2 transgenic mice as early as 6 weeks of age with >90% incidence by 6 months. Analysis of several proliferation/differentiation markers indicated that erbB2 overexpression led to epidermal hyperproliferation and a possible delay in epidermal differentiation. Transgenic mice were also hypersensitive to the proliferative effects of the skin tumor promoter, 12-0-tetradecanoylphorbol-13-acetate (TPA) and were more sensitive to two-stage carcinogenesis. Elevations in EGFr and erbB2 protein as well as erbB2:EGFr and erbB2:erbB3 heterodimers were observed in skin of the erbB2 transgenic mice. Phosphotyrosine levels of the EGFr, erbB2 and erbB3 proteins were also elevated. These results indicate an important role for erbB2 signaling in epidermal growth, development and neoplasia. Oncogene (2000) 19, 4243 - 4254

Indexed as

Gene Expression RegulationGenes, erbB-2TransgenesAnimalsCarcinogensCarcinoma, Squamous CellCattleCell DifferentiationCell DivisionCell Transformation, NeoplasticCocarcinogenesisDimerizationDisease ProgressionEpidermisErb-b2 Receptor Tyrosine KinasesErbB ReceptorsCarcinogensErb-b2 Receptor Tyrosine KinasesErbB ReceptorsKeratinsNeoplasm ProteinsReceptor, ErbB-3Recombinant Fusion ProteinsTetradecanoylphorbol Acetate

Identifiers

PMID10980598
OpenAlexW2071895262

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.