Evidence map›Paper›PMID 12429844›Full record

ArticleMolecular biology of the cell2002

Differential regulation of tumor angiogenesis by distinct ErbB homo- and heterodimers.

Lily Yen, Naciba Benlimame, Zeng-Rong Nie, Dingzhang Xiao, Taiqi Wang, Ala-Eddin Al Moustafa, Hiroyasu Esumi, Julie Milanini, Nancy E Hynes, Gilles Pages and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 126 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  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

11 authors at 6 institutions in 4 countries.

Lily YenLady Davis Institute for Medical Research of the Sir Mortimer B Davis Jewish General Hospital, Department of Medicine and McGill Centre for Translational Research in Cancer, McGill University, Montreal, Quebec, H3T 1E2, Canada.
Naciba Benlimame
Zeng-Rong Nie
Dingzhang Xiao
Taiqi Wang
Ala-Eddin Al Moustafa
Hiroyasu Esumi
Julie Milanini
Nancy E Hynes
Gilles Pages
Moulay A Alaoui-Jamali
McGill University · CAJewish General Hospital · CACentre National de la Recherche Scientifique · FRFriedrich Miescher Institute · CHInstitut de Chimie de Nice · FRNational Cancer Center Hospital East · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interactions between cancer cells and their microenvironment are critical for the development and progression of solid tumors. This study is the first to examine the role of all members of the ErbB tyrosine kinase receptors (epidermal growth factor receptor [EGFR], ErbB-2, ErbB-3, or ErbB-4), expressed singly or as paired receptor combinations, in the regulation of angiogenesis both in vitro and in vivo. Comparison of all receptor combinations reveals that EGFR/ErbB-2 and ErbB-2/ErbB-3 heterodimers are the most potent inducers of vascular endothelial growth factor (VEGF) mRNA expression compared with EGFR/ErbB-3, EGFR/ErbB-4, ErbB-2/ErbB-4, and ErbB-3/ErbB-4. Immunohistochemistry of tumor xenografts overexpressing these heterodimers shows increased VEGF expression and remarkably enhanced vascularity. Enhanced VEGF expression is associated with increased VEGF transcription. Deletional analysis reveals that ErbB-mediated transcriptional up-regulation of VEGF involves a hypoxia-inducible factor 1-independent responsive region located between nucleotides -88 to -66 of the VEGF promoter. Mutational analysis reveals that the Sp-1 and AP-2 transcription factor binding elements within this region are required for up-regulation of VEGF by heregulin beta1 and that this up-regulation is dependent on the activity of extracellular signal-related protein kinases. These results emphasize the biological implications of cell signaling diversity among members of the ErbB receptor family in regulation of the tumor microenvironment.

Indexed as

Neovascularization, PathologicAdenocarcinomaAnimalsButadienesCell LineDimerizationDNA-Binding ProteinsEndothelial Growth FactorsEnzyme InhibitorsErb-b2 Receptor Tyrosine KinasesErbB ReceptorsGenes, ReporterHumansImmunohistochemistryIntercellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsButadienesDNA-Binding ProteinsEndothelial Growth FactorsEnzyme InhibitorsErb-b2 Receptor Tyrosine KinasesERBB4 protein, humanErbb4 protein, mouseErbB Receptorsheregulin beta1Intercellular Signaling Peptides and ProteinsKLF12 protein, humanKruppel-Like Transcription FactorsLymphokinesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein KinasesNeuregulin-1NitrilesReceptor, ErbB-3Receptor, ErbB-4Recombinant Fusion ProteinsSp1 Transcription FactorTranscription FactorsU 0126Vascular Endothelial Growth Factor AVascular Endothelial Growth Factors

Identifiers

PMID12429844
PMCPMC133612
OpenAlexW2165845069

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.