Evidence map›Paper›PMID 26663425›Full record

ArticleExperimental dermatology2016

Extracellular superoxide dismutase deficiency impairs wound healing in advanced age by reducing neovascularization and fibroblast function.

Toshihiro Fujiwara, Dominik Duscher, Kristine C Rustad, Revanth Kosaraju, Melanie Rodrigues, Alexander J Whittam, Michael Januszyk, Zeshaan N Maan, Geoffrey C Gurtner

Open access · greenAbstract read
In one paragraph

Article in Experimental dermatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  8. Review
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  13. Article
  14. Role of Melatonin in Angiotensin and Aging.Molecules (Basel, Switzerland) · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Impaired Neovascularization in Aging.Advances in wound care · 2020
    Review
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Toshihiro FujiwaraDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Dominik DuscherDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Kristine C RustadDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Revanth KosarajuDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Melanie RodriguesDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Alexander J WhittamDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Michael JanuszykDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Zeshaan N MaanDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Geoffrey C GurtnerDivision of Plastic Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Stanford University · US

Funding

POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
Targeting HIF-1 alpha Dysfunction in Complications of AgingR01AG025016 · NIA · STANFORD UNIVERSITY · PI GURTNER, GEOFFREY C · 2004 to 2015
$3.5M
NIA NIH HHS R01 AG025016NIA NIH HHS R01-AG025016NLM NIH HHS T15 LM007033
6 · The paper itself

Abstract

Advanced age is characterized by impairments in wound healing, and evidence is accumulating that this may be due in part to a concomitant increase in oxidative stress. Extended exposure to reactive oxygen species (ROS) is thought to lead to cellular dysfunction and organismal death via the destructive oxidation of intra-cellular proteins, lipids and nucleic acids. Extracellular superoxide dismutase (ecSOD/SOD3) is a prime antioxidant enzyme in the extracellular space that eliminates ROS. Here, we demonstrate that reduced SOD3 levels contribute to healing impairments in aged mice. These impairments include delayed wound closure, reduced neovascularization, impaired fibroblast proliferation and increased neutrophil recruitment. We further establish that SOD3 KO and aged fibroblasts both display reduced production of TGF-β1, leading to decreased differentiation of fibroblasts into myofibroblasts. Taken together, these results suggest that wound healing impairments in ageing are associated with increased levels of ROS, decreased SOD3 expression and impaired extracellular oxidative stress regulation. Our results identify SOD3 as a possible target to correct age-related cellular dysfunction in wound healing.

Indexed as

AgingNeovascularization, PhysiologicWound HealingAnimalsAntioxidantsCell ProliferationFibroblastsMaleMiceMice, Inbred C57BLMice, KnockoutMutationNeutrophilsOxidative StressOxygenReactive Oxygen SpeciesAntioxidantsOxygenReactive Oxygen SpeciesSod3 protein, mouseSuperoxide DismutaseTransforming Growth Factor beta1ageingmyofibroblastoxidative stresssuperoxide dismutasewound healing

Identifiers

PMID26663425
PMCPMC4998179
OpenAlexW2206396087

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.