Evidence map›Paper›PMID 23083077›Full record

ArticleInternational journal of radiation biology2013

Inhibition of radiation-induced skin fibrosis with imatinib.

Jason A Horton, Eun Joo Chung, Kathryn E Hudak, Anastasia Sowers, Angela Thetford, Ayla O White, James B Mitchell, Deborah E Citrin

Open access · greenAbstract read
In one paragraph

Article in International journal of radiation biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 2-Methoxyestradiol Inhibits Radiation-Induced Skin Injuries.International journal of molecular sciences · 2022
    Article
  6. Article
  7. C1222C Deletion in Exon 8 ofFrontiers in oncology · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Radiation-induced fibrosis: mechanisms and implications for therapy.Journal of cancer research and clinical oncology · 2015
    Review
  14. Article
  15. Review
  16. Article
  17. 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

8 authors at 2 institutions in 1 country.

Jason A HortonRadiation Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Eun Joo Chung
Kathryn E Hudak
Anastasia Sowers
Angela Thetford
Ayla O White
James B Mitchell
Deborah E Citrin
National Cancer Institute · USCenter for Cancer Research · US

Funding

Mechanisms of Normal Tissue Toxicity From IrradiationZIABC010850 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CITRIN, DEBORAH · 2009 to 2025
$19.4M
Modulation of Therapeutic ResponseZIASC006321 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI MITCHELL, JAMES · 2009 to 2025
$17.3M
Intramural NIH HHS ZIA BC010850
6 · The paper itself

Abstract

purposeDermal fibrosis is a disabling late toxicity of radiotherapy. Several lines of evidence suggest that overactive signaling via the Platelet-derived growth factor receptor-beta (PDGFR-β) and V-abl Abelson murine leukemia viral oncogene homolog 1 (cAbl) may be etiologic factors in the development of radiation-induced fibrosis. We tested the hypothesis that imatinib, a clinically available inhibitor of PDGFR-β, Mast/stem cell growth factor receptor (c-kit) and cAbl, would reduce the severity of dermal fibrosis in a murine model. MATERIALS AND

methodsThe right hind legs of female C3H/HeN mice were exposed to 35 Gy of X-rays. Cohorts of mice were maintained on chow formulated with imatinib 0.5 mg/g or control chow for the duration of the experiment. Bilateral hind limb extension was measured serially to assess fibrotic contracture. Immunohistochemistry and biochemical assays were used to evaluate the levels of collagen and cytokines implicated in radiation-induced fibrosis.

resultsImatinib treatment significantly reduced hind limb contracture and dermal thickness after irradiation. Immunohistochemical studies demonstrated a substantial reduction in PDGFR-β phosphorylation. We also observed reduced Transforming Growth factor-β (TGF-β) and collagen expression in irradiated skin of imatinib-treated mice, suggesting that imatinib may suppress the fibrotic process by interrupting cross-talk between these pathways.

conclusionsTaken together, these results support that imatinib may be a useful agent in the prevention and treatment of radiation-induced dermal fibrosis.

Indexed as

AnimalsBenzamidesFemaleFibrosisImatinib MesylateMiceMice, Inbred C3HPhosphorylationPiperazinesProto-Oncogene Proteins c-ablProto-Oncogene Proteins c-kitPyrimidinesRadiation Injuries, ExperimentalRadiation-Protective AgentsReceptor, Platelet-Derived Growth Factor betaSignal TransductionBenzamidesImatinib MesylatePiperazinesProto-Oncogene Proteins c-ablProto-Oncogene Proteins c-kitPyrimidinesRadiation-Protective AgentsReceptor, Platelet-Derived Growth Factor betaTransforming Growth Factor beta1

Identifiers

PMID23083077
PMCPMC7511984
OpenAlexW2113765482

What OpenQuestion holds

Textmetadata
LicenceTDM
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.