Evidence map›Paper›PMID 24434934›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

Strengthening the skin with topical delivery of keratinocyte growth factor-1 using a novel DNA plasmid.

Chunqing Dou, Frank Lay, Amir Mehdi Ansari, Donald J Rees, Ali Karim Ahmed, Olga Kovbasnjuk, Aerielle E Matsangos, Junkai Du, Sayed Mohammad Hosseini, Charles Steenbergen and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Glycosaminoglycans: Sweet as Sugar Targets for Topical Skin Anti-Aging.Clinical, cosmetic and investigational dermatology · 2021
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Dendritic epidermal T cells facilitate wound healing in diabetic mice.American journal of translational research · 2016
    Article
  13. Nucleic acid delivery into skin for the treatment of skin disease: Proofs-of-concept, potential impact, and remaining challenges.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  14. 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

16 authors at 3 institutions in 2 countries.

Chunqing Dou1] Department of Hepatobiliary Surgery, The First Affiliated Hospital of Chinese PLA General Hospital, Beijing, China [2] Department of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Frank LayDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Amir Mehdi AnsariDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Donald J ReesDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Ali Karim AhmedDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Olga KovbasnjukDepartment of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Aerielle E MatsangosDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Junkai DuDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sayed Mohammad HosseiniDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Charles SteenbergenDepartment of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Karen Fox-TalbotDepartment of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Aaron T TaborGenArmor, Winston Salem, North Carolina, USA.
James A WilliamsNature Technology Corporation, Lincoln, Nebraska, USA.
Lixin LiuDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Guy P MartiDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
John W HarmonDepartment of Surgery and Hendrix Burn/Wound Laboratory, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins University · USJohns Hopkins Medicine · USNature Technology Corporation (United States) · US

Funding

Translational Research Enhancement CoreP30DK089502 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI ZACHOS, NICHOLAS CONSTANTINE · 2011 to 2020
$12.0M
eukaryotic expression vectors resistant to transgene silencingR44GM080768 · NIGMS · NATURE TECHNOLOGY CORPORATION · PI WILLIAMS, JAMES · 2011 to 2012
$1.1M
Improve Wound Healing with HIF-CA5 DNA Vector and ElectroporationR41GM093023 · NIGMS · CANTON BIOTECHNOLOGIES, INC. · PI HARMON, JOHN W · 2010 to 2010
$173k
NIDDK NIH HHS P30 DK089502NIGMS NIH HHS R41 GM093023NIGMS NIH HHS R44 GM080768NIGMS NIH HHS R44 GM080768-02
6 · The paper itself

Abstract

Fragile skin, susceptible to decubitus ulcers and incidental trauma, is a problem particularly for the elderly and for those with spinal cord injury. Here, we present a simple approach to strengthen the skin by the topical delivery of keratinocyte growth factor-1 (KGF-1) DNA. In initial feasibility studies with the novel minimalized, antibiotic-free DNA expression vector, NTC8385-VA1, the reporter genes luciferase and enhanced green fluorescent protein were delivered. Transfection was documented when luciferase expression significantly increased after transfection. Microscopic imaging of enhanced green fluorescent protein-transfected skin showed green fluorescence in hair follicles, hair shafts, and dermal and superficial epithelial cells. With KGF-1 transfection, KGF-1 mRNA level and protein production were documented with quantitative reverse transcriptase-polymerase chain reaction and immunohistochemistry, respectively. Epithelial thickness of the transfected skin in the KGF group was significantly increased compared with the control vector group (26 ± 2 versus 16 ± 4 µm) at 48 hours (P = 0.045). Dermal thickness tended to be increased in the KGF group (255 ± 36 versus 162 ± 16 µm) at 120 hours (P = 0.057). Biomechanical assessment showed that the KGF-1-treated skin was significantly stronger than control vector-transfected skin. These findings indicate that topically delivered KGF-1 DNA plasmid can increase epithelial thickness and strength, demonstrating the potential of this approach to restore compromised skin.

Indexed as

Genetic TherapyGene Transfer TechniquesAdministration, TopicalAnimalsDNAFibroblast Growth Factor 7HumansMicePlasmidsSkin AbnormalitiesWound HealingDNAFibroblast Growth Factor 7

Identifiers

PMID24434934
PMCPMC3982499
OpenAlexW2032586220

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.