Evidence map›Paper›PMID 23975425›Full record

ArticleOncogene2014

N-cadherin/FGFR promotes metastasis through epithelial-to-mesenchymal transition and stem/progenitor cell-like properties.

X Qian, A Anzovino, S Kim, K Suyama, J Yao, J Hulit, G Agiostratidou, N Chandiramani, H M McDaid, C Nagi and 4 more

Abstract read
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 126 citations in OpenAlex.

  1. Article
  2. Breast Cancer Progression by the FGF/FGFR Axis: A Metabolic Perspective.Journal of mammary gland biology and neoplasia · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Dual-Hit Strategy for Therapeutic Targeting of Pancreatic Cancer in Patient-Derived Xenograft Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. [Frontiers in oncology · 2023
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

15 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

14 authors at 4 institutions in 2 countries.

X QianDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
A AnzovinoDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
S KimDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
K SuyamaDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
J YaoDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
J HulitManchester Breast Centre and Breakthrough Breast Cancer Research Unit, Paterson Institute for Cancer Research, University of Manchester, Manchester, UK.
G AgiostratidouDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
N ChandiramaniDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
H M McDaidDepartment of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
C NagiDepartment of Pathology, Mount Sinai School of Medicine, New York, NY, USA.
H W CohenDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY, USA.
G R PhillipsDepartment of Neuroscience, Mount Sinai School of Medicine, New York, NY, USA.
L NortonDepartment of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
R B HazanDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine · USIcahn School of Medicine at Mount Sinai · USCancer Research UK Manchester Institute · GBMemorial Sloan Kettering Cancer Center · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025750 · NCRR · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SHAMOON, HARRY · 2008 to 2011
$20.5M
TAXOL--MECHANISMS OF ACTION AND RESISTANCER01CA077263 · NCI · YESHIVA UNIVERSITY · PI HORWITZ, SUSAN BAND, MCDAID, HAYLEY M. · 1998 to 2019
$7.8M
EMT, Extravasation and metastasis by N-Cadherin signalingR01CA135061 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI HAZAN, RACHEL B · 2009 to 2013
$1.7M
Clinical and Translational Science Award-K12KL2RR025749 · NCRR · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SHAMOON, HARRY · 2008 to 2011
$991k
Clinical and Translational Science Award-T32 (TL1)TL1RR025748 · NCRR · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SHAMOON, HARRY · 2008 to 2011
$385k
NCATS NIH HHS UL1 TR001073NCI NIH HHS 1R01 CA135061-01A1NCI NIH HHS P30 CA013330NCI NIH HHS R01 CA077263NCI NIH HHS R01 CA135061NCRR NIH HHS KL2 RR025749NCRR NIH HHS KL2RR025749NCRR NIH HHS TL1 RR025748NCRR NIH HHS TL1RR025748NCRR NIH HHS UL1 RR025750NCRR NIH HHS UL1RR025750
6 · The paper itself

Abstract

N-cadherin and HER2/neu were found to be co-expressed in invasive breast carcinomas. To test the contribution of N-cadherin and HER2 in mammary tumor metastasis, we targeted N-cadherin expression in the mammary epithelium of the MMTV-Neu mouse. In the context of ErbB2/Neu, N-cadherin stimulated carcinoma cell invasion, proliferation and metastasis. N-cadherin caused fibroblast growth factor receptor (FGFR) upmodulation, resulting in epithelial-to-mesenchymal transition (EMT) and stem/progenitor like properties, involving Snail and Slug upregulation, mammosphere formation and aldehyde dehydrogenase activity. N-cadherin potentiation of the FGFR stimulated extracellular signal regulated kinase (ERK) and protein kinase B (AKT) phosphorylation resulting in differential effects on metastasis. Although ERK inhibition suppressed cyclin D1 expression, cell proliferation and stem/progenitor cell properties, it did not affect invasion or EMT. Conversely, AKT inhibition suppressed invasion through Akt 2 attenuation, and EMT through Snail inhibition, but had no effect on cyclin D1 expression, cell proliferation or mammosphere formation. These findings suggest N-cadherin/FGFR has a pivotal role in promoting metastasis through differential regulation of ERK and AKT, and underscore the potential for targeting the FGFR in advanced ErbB2-amplified breast tumors.

Indexed as

Epithelial-Mesenchymal TransitionAldehyde DehydrogenaseAnimalsBenzamidesBreast NeoplasmsCadherinsCell MovementCell ProliferationCyclin D1DiphenylamineErb-b2 Receptor Tyrosine KinasesExtracellular Signal-Regulated MAP KinasesFemaleHumansLung NeoplasmsMAP Kinase Kinase 1Akt1 protein, mouseAkt2 protein, mouseAkt3 protein, mouseAldehyde DehydrogenaseBenzamidesCadherinsCcnd1 protein, mouseCyclin D1DiphenylamineERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesExtracellular Signal-Regulated MAP KinasesMap2k1 protein, mouseMAP Kinase Kinase 1mirdametinibPD 173074Proto-Oncogene Proteins c-aktPyrimidinesReceptors, Fibroblast Growth FactorRNA, Small InterferingSNAI1 protein, humanSnai2 protein, mouseSnail Family Transcription FactorsTranscription Factors

Identifiers

PMID23975425
PMCPMC4051865
OpenAlexW2161273389

What OpenQuestion holds

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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.