Evidence map›Paper›PMID 23593394›Full record

ArticlePloS one2013

Endothelial protein C receptor function in murine and human breast cancer development.

Florence Schaffner, Naho Yokota, Tatiana Carneiro-Lobo, Maki Kitano, Michael Schaffer, G Mark Anderson, Barbara M Mueller, Charles T Esmon, Wolfram Ruf

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
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

41 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Tumour Stem Cells in Breast Cancer.International journal of molecular sciences · 2022
    Review
  9. Roles of factor Xa beyond coagulation.Journal of thrombosis and thrombolysis · 2021
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  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

9 authors.

Florence SchaffnerDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, California, United States of America.
Naho Yokota
Tatiana Carneiro-Lobo
Maki Kitano
Michael Schaffer
G Mark Anderson
Barbara M Mueller
Charles T Esmon
Wolfram Ruf

Funding

SIGNALING OF TISSUE FACTOR IN CELL ADHESIONR01HL060742 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI RUF, WOLFRAM · 1998 to 2017
$6.4M
NHLBI NIH HHS HL-60742NHLBI NIH HHS R01 HL060742
6 · The paper itself

Abstract

Several markers identify cancer stem cell-like populations, but little is known about the functional roles of stem cell surface receptors in tumor progression. Here, we show that the endothelial protein C receptor (EPCR), a stem cell marker in hematopoietic, neuronal and epithelial cells, is crucial for breast cancer growth in the orthotopic microenvironment of the mammary gland. Mice with a hypomorphic allele of EPCR show reduced tumor growth in the PyMT-model of spontaneous breast cancer development and deletion of EPCR in established PyMT tumor cells significantly attenuates transplanted tumor take and growth. We find expansion of EPCR(+) cancer stem cell-like populations in aggressive, mammary fat pad-enhanced human triple negative breast cancer cells. In this model, EPCR-expressing cells have markedly increased mammosphere- and tumor-cell initiating activity compared to another stable progenitor-like subpopulation present at comparable frequency. We show that receptor blocking antibodies to EPCR specifically attenuate in vivo tumor growth initiated by either EPCR(+) cells or the heterogenous mixture of EPCR(+) and EPCR(-) cells. Furthermore, we have identified tumor associated macrophages as a major source for recognized ligands of EPCR, suggesting a novel mechanism by which cancer stem cell-like populations are regulated by innate immune cells in the tumor microenvironment.

Indexed as

Adipose TissueAnimalsAntigens, CDBreast NeoplasmsCell Line, TumorCell ProliferationCell Transformation, NeoplasticCluster AnalysisDisease Models, AnimalEndothelial Protein C ReceptorFemaleGene Expression ProfilingGlycoproteinsHumansMacrophagesMammary Glands, AnimalAntigens, CDEndothelial Protein C ReceptorGlycoproteinsPROCR protein, humanProcr protein, mouseReceptors, Cell Surface

Identifiers

PMID23593394
PMCPMC3621887

What OpenQuestion holds

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LicenceCC BY
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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.