Evidence map›Paper›PMID 14695345›Full record

ArticleThe American journal of pathology2004

A mouse model of uterine leiomyosarcoma.

Katerina Politi, Matthias Szabolcs, Peter Fisher, Ana Kljuic, Thomas Ludwig, Argiris Efstratiadis

Open access · greenAbstract readComparative Study
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. The biology of uterine sarcomas: A review and update.Molecular and clinical oncology · 2013
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Myc is a Notch1 transcriptional target and a requisite for Notch1-induced mammary tumorigenesis in mice.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  13. 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 1 country.

Katerina PolitiDepartment of Genetics and Development, Columbia University, New York, New York, USA.
Matthias Szabolcs
Peter Fisher
Ana Kljuic
Thomas Ludwig
Argiris Efstratiadis
Columbia University · USCancer Genetics (United States) · US

Funding

The role of PTEN in basal-like breast cancerP01CA097403 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SZABOLCS, MATTHIAS · 2003 to 2013
$18.2M
CELL, MOLECULAR AND DEVELOPMENTAL BIOLOGY OF CANCERT32CA009503 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI GAUTIER, JEAN · 1985 to 2016
$6.8M
TUMOR SUPPRESSORS INVOLVED IN MULTIPLE TUMOR TYPESP01CA075553 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EDELMAN, ISIDORE · 1998 to 2001
$2.5M
NCI NIH HHS P01 CA097403NCI NIH HHS P01 CA75553NCI NIH HHS P01 CA97403NCI NIH HHS T32 CA009503NCI NIH HHS T32 CA09503
6 · The paper itself

Abstract

We are using an approach that is based on the cre/loxP recombination process and involves a binary system of Cre-producing and Cre-responding transgenic mice to achieve ubiquitous or tissue-specific expression of oncoproteins. To develop mouse models of tumorigenesis, Cre-producers are mated with responder animals carrying a dormant oncogene targeted into the 3' untranslated region of the locus encoding cytoplasmic beta-actin (actin cassette). Production of oncoprotein from a bicistronic message is accomplished in bitransgenic progeny by Cre-mediated excision of a segment flanked by loxP sites that is located upstream from the oncogenic sequence. Widespread Cre-dependent activation and expression of an actin-cassette transgene encoding the T antigens of the SV40 early region (SVER) commencing in embryos was compatible with normal development and did not impair viability. However, at approximately 3 months of age, all female animals developed massive uterine leiomyosarcomas, whereas practically all males exhibited enormously enlarged seminal vesicles because of pronounced hyperplasia of the smooth muscle layers. In addition, because of smooth muscle hyperproliferation, marked dilation of the gallbladder was observed in mice of both sexes. To begin exploring aberrant signaling events in the SVER-triggered tumorigenic pathways, we analyzed the expression profile of leiomyosarcomas by DNA microarray analysis.

Indexed as

Disease Models, AnimalGene Expression Regulation, NeoplasticActinsAnimalsAntigens, Polyomavirus TransformingFemaleGallbladderGene Expression ProfilingHyperplasiaImmunoblottingIntegrasesLeiomyomaLeiomyosarcomaMaleMiceMice, TransgenicActinsAntigens, Polyomavirus TransformingCre recombinaseIntegrasesViral Proteins

Identifiers

PMID14695345
PMCPMC1602220
OpenAlexW1984804388

What Socratic 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 Socratic graph.