Evidence map›Paper›PMID 25420155›Full record

ArticlePloS one2014

Hypoxia-controlled EphA3 marks a human endometrium-derived multipotent mesenchymal stromal cell that supports vascular growth.

Catherine To, Rae H Farnsworth, Mary E Vail, Chanly Chheang, Caroline E Gargett, Carmel Murone, Carmen Llerena, Andrew T Major, Andrew M Scott, Peter W Janes and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Identification of potent pan-ephrin receptor kinase inhibitors using DNA-encoded chemistry technology.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. Eph Receptors in Cancer.Biomedicines · 2023
    Review
  9. Eph-Ephrin Signaling Mediates Cross-Talk Within the Bone Microenvironment.Frontiers in cell and developmental biology · 2021
    Review
  10. Antibody Targeting of Eph Receptors in Cancer.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  11. Review
  12. 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 3 institutions in 1 country.

Catherine ToDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Rae H FarnsworthDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Mary E VailDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Chanly ChheangDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Caroline E GargettMIMR-PHI Institute for Medical Research, Clayton, Victoria, Australia.
Carmel MuroneLudwig Institute for Cancer Research, Olivia Newton-John Cancer & Wellness Centre, Melbourne, Victoria, Australia.
Carmen LlerenaDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Andrew T MajorDepartment of Anatomy & Developmental Biology, Monash University, Melbourne, Victoria, Australia.
Andrew M ScottLudwig Institute for Cancer Research, Olivia Newton-John Cancer & Wellness Centre, Melbourne, Victoria, Australia.
Peter W JanesDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Martin LackmannDepartment of Biochemistry & Molecular Biology, Monash University, Melbourne, Victoria, Australia.
Monash University · AULudwig Cancer Research · AUOlivia Newton-John Cancer Wellness & Research Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eph and ephrin proteins are essential cell guidance cues that orchestrate cell navigation and control cell-cell interactions during developmental tissue patterning, organogenesis and vasculogenesis. They have been extensively studied in animal models of embryogenesis and adult tissue regeneration, but less is known about their expression and function during human tissue and organ regeneration. We discovered the hypoxia inducible factor (HIF)-1α-controlled expression of EphA3, an Eph family member with critical functions during human tumour progression, in the vascularised tissue of regenerating human endometrium and on isolated human endometrial multipotent mesenchymal stromal cells (eMSCs), but not in other highly vascularised human organs. EphA3 affinity-isolation from human biopsy tissue yielded multipotent CD29+/CD73+/CD90+/CD146+ eMSCs that can be clonally propagated and respond to EphA3 agonists with EphA3 phosphorylation, cell contraction, cell-cell segregation and directed cell migration. EphA3 silencing significantly inhibited the ability of transplanted eMSCs to support neovascularisation in immunocompromised mice. In accord with established roles of Eph receptors in mediating interactions between endothelial and perivascular stromal cells during mouse development, our findings suggest that HIF-1α-controlled expression of EphA3 on human MSCs functions during the hypoxia-initiated early stages of adult blood vessel formation.

Indexed as

Neovascularization, PhysiologicAdultAnimalsBlotting, WesternCell HypoxiaCells, CulturedEndometriumFemaleGene ExpressionHeterograftsHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMesenchymal Stem CellsMesenchymal Stem Cell TransplantationMice, Inbred BALB CHypoxia-Inducible Factor 1, alpha SubunitReceptor, EphA3

Identifiers

PMID25420155
PMCPMC4242616
OpenAlexW2049615458

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.