Evidence map›Paper›PMID 26415936›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2016

Adenosine A2A receptor plays an important role in radiation-induced dermal injury.

Miguel Perez-Aso, Aránzazu Mediero, Yee Cheng Low, Jamie Levine, Bruce N Cronstein

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-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

15 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Insights from Clinical Trials on AACS pharmacology & translational science · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Adenosine AThe American journal of pathology · 2017
    Article
  12. Review
  13. Loss of CD73 prevents accumulation of alternatively activated macrophages and the formation of prefibrotic macrophage clusters in irradiated lungs.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  14. Inhibition of AFrontiers in pharmacology · 2017
    Article
  15. Purinergic Signalling: Therapeutic Developments.Frontiers in pharmacology · 2017
    Review
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

5 authors at 1 institution in 1 country.

Miguel Perez-Aso*Division of Translational Medicine, Department of Medicine, and New York University Cancer Center, New York University School of Medicine, New York, New York, USA.
Aránzazu Mediero*Division of Translational Medicine, Department of Medicine, and New York University Cancer Center, New York University School of Medicine, New York, New York, USA.
Yee Cheng Low*Division of Translational Medicine, Department of Medicine, and New York University Cancer Center, New York University School of Medicine, New York, New York, USA.
Jamie Levine*Division of Translational Medicine, Department of Medicine, and New York University Cancer Center, New York University School of Medicine, New York, New York, USA.
Bruce N Cronstein*Division of Translational Medicine, Department of Medicine, and New York University Cancer Center, New York University School of Medicine, New York, New York, USA bruce.cronstein@nyumc.org.
New York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Institutional Clinical and Translational Science AwardUL1TR000038 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CRONSTEIN, BRUCE NEIL · 2012 to 2014
$16.8M
The Pharmacology of Dermal Fibrosis R01AR056672 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CRONSTEIN, BRUCE NEIL · 2009 to 2018
$4.6M
Purinergic Stimulation of Bone RegenerationR01AR068593 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COELHO, PAULO G, CRONSTEIN, BRUCE NEIL · 2015 to 2019
$2.8M
The Pharmacology of Dermal FibrosisR56AR056672 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CRONSTEIN, BRUCE NEIL · 2014 to 2014
$373k
NCATS NIH HHS UL1 TR000038NCATS NIH HHS UL1TR000038NCI NIH HHS P30 CA016087NCI NIH HHS P30CA016087NIAMS NIH HHS AR56672NIAMS NIH HHS AR68593NIAMS NIH HHS R01 AR056672NIAMS NIH HHS R01 AR068593NIAMS NIH HHS R56 AR056672
6 · The paper itself

Abstract

Ionizing radiation is a common therapeutic modality and following irradiation dermal changes, including fibrosis and atrophy, may lead to permanent changes. We have previously demonstrated that occupancy of A2A receptor (A2AR) stimulates collagen production, so we determined whether blockade or deletion of A2AR could prevent radiation-induced fibrosis. After targeted irradiation (40 Gy) of the skin of wild-type (WT) or A2AR knockout (A2ARKO) mice, the A2AR antagonist ZM241385 was applied daily for 28 d. In irradiated WT mice treated with the A2AR antagonist, there was a marked reduction in collagen content and skin thickness, and ZM241385 treatment reduced the number of myofibroblasts and angiogenesis. After irradiation, there is an increase in loosely packed collagen fibrils, which is significantly diminished by ZM241385. Irradiation also induced an increase in epidermal thickness, prevented by ZM241385, by increasing the number of proliferating keratinocytes. Similarly, in A2ARKO mice, the changes in collagen alignment, skin thickness, myofibroblast content, angiogenesis, and epidermal hyperplasia were markedly reduced following irradiation. Radiation-induced changes in the dermis and epidermis were accompanied by an infiltrate of T cells, which was prevented in both ZM241385-treated and A2ARKO mice. Radiation therapy is administered to a significant number of patients with cancer, and radiation reactions may limit this therapeutic modality. Our findings suggest that topical application of an A2AR antagonist prevents radiation dermatitis and may be useful in the prevention or amelioration of radiation changes in the skin.

Indexed as

Adenosine A2 Receptor AntagonistsAnimalsCollagenKeratinocytesMiceMice, Inbred C57BLMyofibroblastsRadiodermatitisReceptor, Adenosine A2ATriazinesTriazolesAdenosine A2 Receptor AntagonistsCollagenReceptor, Adenosine A2ATriazinesTriazolesZM 241385radiotherapy lesionsskintherapeuticZM241385

Identifiers

PMID26415936
PMCPMC4684533
OpenAlexW2232156723

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.