Evidence map›Paper›PMID 20189993›Full record

ArticleThe Journal of biological chemistry2010

GATA3 inhibits breast cancer metastasis through the reversal of epithelial-mesenchymal transition.

Wei Yan, Qing Jackie Cao, Richard B Arenas, Brooke Bentley, Rong Shao

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
13.7field-weighted citation impact, top 1% 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

123 citing papers in PubMed, 226 citations in OpenAlex.

  1. The GATA3-RFPL3-ASK1 axis suppresses breast cancer growth and lung metastasis.Apoptosis : an international journal on programmed cell death · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. GATA3 promotes ferroptosis resistance by repressing integrin β1 signaling.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Hormone Signaling in Breast Development and Cancer.Advances in experimental medicine and biology · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

63 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Wei YanPioneer Valley Life Sciences Institute, University of Massachusetts, Springfield, Massachusetts 01107, USA.
Qing Jackie Cao
Richard B Arenas
Brooke Bentley
Rong Shao
Pioneer (United States) · USBaystate Medical Center · US

Funding

Role of a novel angiogenic factor, YKL-40, in breast cancer progressionR01CA120659 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI SHAO, RONG · 2008 to 2012
$1.1M
NCI NIH HHS R01 CA120659
6 · The paper itself

Abstract

GATA3, a transcription factor that regulates T lymphocyte differentiation and maturation, is exclusively expressed in early stage well differentiated breast cancers but not in advanced invasive cancers. However, little is understood regarding its activity and the mechanisms underlying this differential expression in cancers. Here, we employed GATA3-positive, non-invasive (MCF-7) and GATA3-negative, invasive (MDA-MB-231) breast cancer cells to define its role in the transformation between these two distinct phenotypes. Ectopic expression of GATA3 in MDA-MB-231 cells led to a cuboidal-like epithelial phenotype and reduced cell invasive activity. These cells also increased E-cadherin expression but decreased levels of vimentin, N-cadherin, and MMP-9. Further, MDA-MB-231 cells expressing GATA3 grew smaller primary tumors without metastasis compared with larger metastatic tumors derived from control MDA-MB-231 cells in xenografted mice. GATA3 was found to induce E-cadherin expression through binding GATA-like motifs located in the E-cadherin promoter. Blockade of GATA3 using small interfering RNA gene knockdown in MCF-7 cells triggered fibroblastic transformation and cell invasion, resulting in distant metastasis. Studies of human breast cancer showed that GATA3 expression correlated with elevated E-cadherin levels, ER expression, and long disease-free survival. These data suggest that GATA3 drives invasive breast cancer cells to undergo the reversal of epithelial-mesenchymal transition, leading to the suppression of cancer metastasis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntigens, CDBreast NeoplasmsCadherinsCell Line, TumorFemaleGATA3 Transcription FactorHumansMatrix Metalloproteinase 9MiceMice, SCIDNeoplasm InvasivenessNeoplasm MetastasisNeoplasm ProteinsNeoplasm TransplantationAntigens, CDCadherinsCDH2 protein, humanGATA3 protein, humanGATA3 Transcription FactorMatrix Metalloproteinase 9Neoplasm ProteinsRNA, Small InterferingVimentin

Identifiers

PMID20189993
PMCPMC2859565
OpenAlexW2055505762

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.