Evidence map›Paper›PMID 15897912›Full record

ArticleOncogene2005

Human Cripto-1 overexpression in the mouse mammary gland results in the development of hyperplasia and adenocarcinoma.

Christian Wechselberger, Luigi Strizzi, Nicholas Kenney, Morihisa Hirota, Youping Sun, Andreas Ebert, Olivia Orozco, Caterina Bianco, Nadia I Khan, Brenda Wallace-Jones and 4 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. CRIPTO antagonist ALK4Breast cancer research : BCR · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Cripto-1 expression and its prognostic value in human bladder cancer patients.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Targeting the embryonic gene Cripto-1 in cancer and beyond.Expert opinion on therapeutic patents · 2010
    Review
  18. Review
  19. Review
  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

14 authors at 4 institutions in 3 countries.

Christian WechselbergerTumor Growth Factor Section, Mammary Biology and Tumorigenesis Laboratory, National Cancer Institute, Bethesda, MD 20892, USA.
Luigi Strizzi
Nicholas Kenney
Morihisa Hirota
Youping Sun
Andreas Ebert
Olivia Orozco
Caterina Bianco
Nadia I Khan
Brenda Wallace-Jones
Nicola Normanno
Heather Adkins
Michele Sanicola
David S Salomon
National Cancer Institute · USBiogen (United States) · USFreie Universität Berlin · DEIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · IT

Funding

The Role of Cripto in the Pathogenesis of Breast and Colon CancerZIABC009003 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SALOMON, DAVID · 2009 to 2016
$9.4M
THE ROLE OF EGF-RELATED PEPTIDES IN THE PATHOGENESIS OF BREAST AND COLON CANCERZ01BC009003 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SALOMON, DAVID · 1996 to 2008
$2.4M
6 · The paper itself

Abstract

Human Cripto-1 (CR-1) is overexpressed in approximately 80% of human breast, colon and lung carcinomas. Mouse Cr-1 upregulation is also observed in a number of transgenic (Tg) mouse mammary tumors. To determine whether CR-1 can alter mammary gland development and/or may contribute to tumorigenesis in vivo, we have generated Tg mouse lines that express human CR-1 under the transcriptional control of the mouse mammary tumor virus (MMTV). Stable Tg MMTV/CR-1 FVB/N lines expressing different levels of CR-1 were analysed. Virgin female MMTV/CR-1 Tg mice exhibited enhanced ductal branching, dilated ducts, intraductal hyperplasia, hyperplastic alveolar nodules and condensation of the mammary stroma. Virgin aged MMTV/CR-1 Tg mice also possessed persistent end buds. In aged multiparous MMTV/CR-1 mice, the hyperplastic phenotype was most pronounced with multifocal hyperplasias. In the highest CR-1-expressing subline, G4, 38% (12/31) of the multiparous animals aged 12-20 months developed hyperplasias and approximately 33% (11/31) developed papillary adenocarcinomas. The long latency period suggests that additional genetic alterations are required to facilitate mammary tumor formation in conjunction with CR-1. This is the first in vivo study that shows hyperplasia and tumor growth in CR-1-overexpressing animals.

Indexed as

AdenocarcinomaAnimalsCell DivisionDNA, ComplementaryDNA PrimersEpidermal Growth FactorFemaleGPI-Linked ProteinsGrowth SubstancesHyperplasiaIntercellular Signaling Peptides and ProteinsMammary Glands, AnimalMammary Neoplasms, AnimalMembrane GlycoproteinsMiceMice, TransgenicDNA, ComplementaryDNA PrimersEpidermal Growth FactorGPI-Linked ProteinsGrowth SubstancesIntercellular Signaling Peptides and ProteinsMembrane GlycoproteinsNeoplasm ProteinsTDGF1 protein, human

Identifiers

PMID15897912
OpenAlexW2159969939

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.