Evidence map›Paper›PMID 24626992›Full record

ArticleDisease models & mechanisms2014

RUNX2 correlates with subtype-specific breast cancer in a human tissue microarray, and ectopic expression of Runx2 perturbs differentiation in the mouse mammary gland.

Laura McDonald, Nicola Ferrari, Anne Terry, Margaret Bell, Zahra M Mohammed, Clare Orange, Alma Jenkins, William J Muller, Barry A Gusterson, James C Neil and 4 more

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. RUNX2 promotes malignant progression in gastric cancer by regulating COL1A1.Cancer biomarkers : section A of Disease markers · 2021
    Article
  13. Article
  14. Review
  15. RUNX1 Dosage in Development and Cancer.Molecules and cells · 2020
    Review
  16. Article
  17. Review
  18. Review
  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

14 authors at 5 institutions in 2 countries.

Laura McDonaldCancer Research UK Beatson Institute, Switchback Road, Bearsden, Glasgow, G61 1BD, UK.
Nicola Ferrari
Anne Terry
Margaret Bell
Zahra M Mohammed
Clare Orange
Alma Jenkins
William J Muller
Barry A Gusterson
James C Neil
Joanne Edwards
Joanna S Morris
Ewan R Cameron
Karen Blyth
University of Glasgow · GBMRC University of Glasgow Centre for Virus Research · GBCancer Research UK Scotland Institute · GBCancer Research UK · GBMcGill University · CA

Funding

Cancer Research UK 11951Worldwide Cancer Research 08-0484
6 · The paper itself

Abstract

RUNX2, a master regulator of osteogenesis, is oncogenic in the lymphoid lineage; however, little is known about its role in epithelial cancers. Upregulation of RUNX2 in cell lines correlates with increased invasiveness and the capacity to form osteolytic disease in models of breast and prostate cancer. However, most studies have analysed the effects of this gene in a limited number of cell lines and its role in primary breast cancer has not been resolved. Using a human tumour tissue microarray, we show that high RUNX2 expression is significantly associated with oestrogen receptor (ER)/progesterone receptor (PR)/HER2-negative breast cancers and that patients with high RUNX2 expression have a poorer survival rate than those with negative or low expression. We confirm RUNX2 as a gene that has a potentially important functional role in triple-negative breast cancer. To investigate the role of this gene in breast cancer, we made a transgenic model in which Runx2 is specifically expressed in murine mammary epithelium under the control of the mouse mammary tumour virus (MMTV) promoter. We show that ectopic Runx2 perturbs normal development in pubertal and lactating animals, delaying ductal elongation and inhibiting lobular alveolar differentiation. We also show that the Runx2 transgene elicits age-related, pre-neoplastic changes in the mammary epithelium of older transgenic animals, suggesting that elevated RUNX2 expression renders such tissue more susceptible to oncogenic changes and providing further evidence that this gene might have an important, context-dependent role in breast cancer.

Indexed as

Cell DifferentiationTissue Array AnalysisAnimalsBreast NeoplasmsCore Binding Factor Alpha 1 SubunitDNA-Binding ProteinsFemaleHumansHyperplasiaLactationMammary Glands, AnimalMammary Tumor Virus, MouseMice, TransgenicMiddle AgedParityPrecancerous ConditionsCore Binding Factor Alpha 1 SubunitDNA-Binding ProteinsElf5 protein, mouseRUNX2 protein, humanRunx2 protein, mouseSTAT5 Transcription FactorTranscription FactorsBreast cancerMammary developmentRUNX2Transgenic model

Identifiers

PMID24626992
PMCPMC4007404
OpenAlexW2119851259

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.