Evidence map›Paper›PMID 23784441›Full record

ArticleGene therapy2013

Combination of HIF-1α gene transfection and HIF-1-activated bone marrow-derived angiogenic cell infusion improves burn wound healing in aged mice.

J Du, L Liu, F Lay, Q Wang, C Dou, X Zhang, S M Hosseini, A Simon, D J Rees, A K Ahmed and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Modelling physical resilience in ageing mice.Mechanisms of ageing and development · 2019
    Review
  7. Article
  8. Deferoxamine can prevent pressure ulcers and accelerate healing in aged mice.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2018
    Article
  9. Review
  10. Review
  11. Article
  12. Burn wound healing properties of asiaticoside and madecassoside.Experimental and therapeutic medicine · 2016
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Chronic wound repair and healing in older adults: current status and future research.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    Article
  19. 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

16 authors at 4 institutions in 1 country.

J Du1] Department of General Surgery, First Hospital Affiliated to Medical School, Xi'an Jiaotong University, Xi'an, China [2] Hendrix Burn Laboratory, Section of Surgical Sciences, Department of Surgery, Johns Hopkins Bayview Medical Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
L Liu
F Lay
Q Wang
C Dou
X Zhang
S M Hosseini
A Simon
D J Rees
A K Ahmed
R Sebastian
K Sarkar
S Milner
G P Marti
G L Semenza
J W Harmon
University of Baltimore · USJohns Hopkins Bayview Medical Center · USJohns Hopkins Medicine · USJohns Hopkins University · US

Funding

Improve Wound Healing with HIF-CA5 DNA Vector and ElectroporationR41GM093023 · NIGMS · CANTON BIOTECHNOLOGIES, INC. · PI HARMON, JOHN W · 2010 to 2010
$173k
NIGMS NIH HHS R01 GM093023
6 · The paper itself

Abstract

Impaired burn wound healing in the elderly represents a major clinical problem. Hypoxia-inducible factor-1 (HIF-1) is a transcriptional activator that orchestrates the cellular response to hypoxia. Its actions in dermal wounds promote angiogenesis and improve healing. In a murine burn wound model, aged mice had impaired wound healing associated with reduced levels of HIF-1. When gene therapy with HIF-1 alone did not correct these deficits, we explored the potential benefit of HIF-1 gene therapy combined with the intravenous infusion of bone marrow-derived angiogenic cells (BMDACs) cultured with dimethyloxalylglycine (DMOG). DMOG is known to reduce oxidative degradation of HIF-1. The mice treated with a plasmid DNA construct expressing a stabilized mutant form of HIF-1α (CA5-HIF-1α)+BMDACs had more rapid wound closure. By day 17, there were more mice with completely closed wounds in the treated group (χ(2), P=0.05). The dermal blood flow measured by laser Doppler showed significantly increased wound perfusion on day 11. Homing of BMDACs to the burn wound was dramatically enhanced by CA5-HIF-1α gene therapy. HIF-1α mRNA expression in the burn wound was increased after transfection with CA5-HIF-1α plasmid. Our findings offer insight into the pathophysiology of burns in the elderly and point to potential targets for developing new therapeutic strategies.

Indexed as

Bone Marrow TransplantationGenetic TherapyTransfectionAdenoviridaeAgingAnimalsBone Marrow CellsBurnsCells, CulturedCombined Modality TherapyDisease Models, AnimalFemaleGenetic VectorsHumansHypoxia-Inducible Factor 1, alpha SubunitMaleHypoxia-Inducible Factor 1, alpha Subunit

Identifiers

PMID23784441
OpenAlexW2076020058

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.