Evidence map›Paper›PMID 16816378›Full record

ArticleThe American journal of pathology2006

Disabled-2 heterozygous mice are predisposed to endometrial and ovarian tumorigenesis and exhibit sex-biased embryonic lethality in a p53-null background.

Dong-Hua Yang, Zia Fazili, Elizabeth R Smith, Kathy Qi Cai, Andres Klein-Szanto, Cynthia Cohen, Ira R Horowitz, Xiang-Xi Xu

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Endocytosis and Physiology: Insights from Disabled-2 Deficient Mice.Frontiers in cell and developmental biology · 2016
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. BRCA1-mediated signaling pathways in ovarian carcinogenesis.Functional & integrative genomics · 2012
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Migrating with myosin VI.The American journal of pathology · 2006
    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 1 country.

Dong-Hua YangOvarian Cancer and Tumor Cell Biology Programs, Fox Chase Cancer Center, 333 Cottman Ave., Philadelphia, PA 19111-2497, USA.
Zia Fazili
Elizabeth R Smith
Kathy Qi Cai
Andres Klein-Szanto
Cynthia Cohen
Ira R Horowitz
Xiang-Xi Xu
Fox Chase Cancer Center · USEmory University · USGynecologic Oncology Group · US

Funding

Ovarian Cancer: Epithelial DedifferentiationR01CA079716 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI XU, XIANGXI MIKE · 1999 to 2015
$4.8M
Epithelial Positioning Organization and Ovarian CancerR01CA095071 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI XU, XIANGXI MIKE · 2002 to 2010
$3.2M
DAB2 AND RAS REGULATIONR01CA075389 · NCI · INSTITUTE FOR CANCER RESEARCH · PI XU, XIANGXI MIKE · 1997 to 2001
$534k
NCI NIH HHS R01 CA079716NCI NIH HHS R01 CA095071NCI NIH HHS R01 CA75389NCI NIH HHS R01 CA79716
6 · The paper itself

Abstract

Disabled-2 (Dab2) is a phosphoprotein involved in cellular signal transduction and endocytic trafficking. The expression of Dab2 is frequently lost or suppressed in several epithelial tumors, and studies of its cellular function and growth suppressive activity when re-expressed in cancer cells led to the suggestion that Dab2 is a tumor suppressor. A role for Dab2 in epithelial cell positioning organization was derived from study of knockout mice: homozygous deletion of dab2 results in early embryonic lethality due to the disorganization of the primitive endoderm, the first epithelium in early embryos. We now report that dab2 heterozygous mice develop uterine hyperplasia and ovarian preneoplastic morphological changes at a high frequency. Crossing into a p53(-/-) background unexpectedly produced few female dab2(+/-):p53(-/-) mice, while the male dab2(+/-):p53(-/-) were born at the expected Mendelian frequency. The tumor-prone phenotype of dab2(+/-) mice provides additional support for a role of human Dab2 as a tumor suppressor, and the sex-biased embryonic lethality suggests a genetic interaction between p53 and dab2 genes in female mice.

Indexed as

Genes, p53Adaptor Proteins, Signal TransducingAdaptor Proteins, Vesicular TransportAdenocarcinomaAnimalsApoptosis Regulatory ProteinsBlotting, WesternCell Line, TumorCell Transformation, NeoplasticEmbryo, MammalianEndometrial NeoplasmsFemaleGenes, Tumor SuppressorHeterozygoteHumansMaleAdaptor Proteins, Signal TransducingAdaptor Proteins, Vesicular TransportApoptosis Regulatory ProteinsDab2 protein, mouse

Identifiers

PMID16816378
PMCPMC1698752
OpenAlexW2094090548

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.