Evidence map›Paper›PMID 26765957›Full record

ArticleThe American journal of pathology2016

The Eyes Absent Proteins in Developmental and Pathological Angiogenesis.

Yuhua Wang, Emmanuel Tadjuidje, Ram Naresh Pandey, James A Stefater, Lois E H Smith, Richard A Lang, Rashmi S Hegde

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. The Eyes Absent Proteins: Unusual HAD Family Tyrosine Phosphatases.International journal of molecular sciences · 2021
    Review
  9. Article
  10. The multi-functional eyes absent proteins.Critical reviews in biochemistry and molecular biology · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. The Eya phosphatase: Its unique role in cancer.The international journal of biochemistry & cell biology · 2018
    Review
  15. Modeling tumor cell adaptations to hypoxia in multicellular tumor spheroids.Journal of experimental & clinical cancer research : CR · 2017
    Review
  16. 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

7 authors at 3 institutions in 1 country.

Yuhua WangDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Emmanuel TadjuidjeDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Ram Naresh PandeyDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
James A StefaterDivision of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Lois E H SmithDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Richard A LangDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Pediatric Ophthalmology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Rashmi S HegdeDivision of Developmental Biology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio. Electronic address: rashmi.hegde@cchmc.org.
Cincinnati Children's Hospital Medical Center · USHarvard University · USUniversity of Cincinnati · US

Funding

Dietary control of angiogenesis in retinopathy modelsR01EY017017 · NEI · BOSTON CHILDREN'S HOSPITAL · PI Zhongjie Fu, Lois Smith · 2006 to 2026
$11.8M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Molecular Mechanisms of Retinal Determination ProteinsR01EY014648 · NEI · CINCINNATI CHILDRENS HOSP MED CTR · PI HEGDE, RASHMI S. · 2004 to 2017
$4.1M
Retinal Microglia and AngiogenesisR01EY021636 · NEI · CINCINNATI CHILDRENS HOSP MED CTR · PI LANG, RICHARD A. · 2012 to 2016
$1.9M
EYA in Retinal AngiogenesisR01EY022917 · NEI · CINCINNATI CHILDRENS HOSP MED CTR · PI HEGDE, RASHMI S. · 2013 to 2016
$1.5M
NEI NIH HHS EY014648NEI NIH HHS EY022917NEI NIH HHS R01 EY014648NEI NIH HHS R01 EY017017NEI NIH HHS R01 EY021636NEI NIH HHS R01 EY022917NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

Management of neoangiogenesis remains a high-value therapeutic goal. A recently uncovered association between the DNA damage repair pathway and pathological angiogenesis could open previously unexplored possibilities for intervention. An attractive and novel target is the Eyes absent (EYA) tyrosine phosphatase, which plays a critical role in the repair versus apoptosis decision after DNA damage. This study examines the role of EYA in the postnatal development of the retinal vasculature and under conditions of ischemia-reperfusion encountered in proliferative retinopathies. We find that the ability of the EYA proteins to promote endothelial cell (EC) migration contributes to a delay in postnatal development of the retinal vasculature when Eya3 is deleted specifically in ECs. By using genetic and chemical biology tools, we show that EYA contributes to pathological angiogenesis in a model of oxygen-induced retinopathy. Both in vivo and in vitro, loss of EYA tyrosine phosphatase activity leads to defective assembly of γ-H2AX foci and thus to DNA damage repair in ECs under oxidative stress. These data reveal the potential utility of EYA tyrosine phosphatase inhibitors as therapeutic agents in inhibiting pathological neovascularization with a range of clinical applications.

Indexed as

DNA RepairAnimalsAnimals, NewbornCell MovementDNA-Binding ProteinsDNA DamageEndothelial CellsEyeFemaleGene DeletionHumansMaleMice, Inbred C57BLNeovascularization, PathologicOxygenProtein Tyrosine PhosphatasesDNA-Binding ProteinsEya3 protein, mouseOxygenProtein Tyrosine Phosphatases

Identifiers

PMID26765957
PMCPMC4816707
OpenAlexW2229972594

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.