Evidence map›Paper›PMID 24675668›Full record

ArticlePloS one2014

Novel anti-microbial peptide SR-0379 accelerates wound healing via the PI3 kinase/Akt/mTOR pathway.

Hideki Tomioka, Hironori Nakagami, Akiko Tenma, Yoshimi Saito, Toshihiro Kaga, Toshihide Kanamori, Nao Tamura, Kazunori Tomono, Yasufumi Kaneda, Ryuichi Morishita

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Wound healing mechanism of antimicrobial peptide cathelicidin-DM.Frontiers in bioengineering and biotechnology · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Bioactive Peptides.Foods (Basel, Switzerland) · 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

10 authors at 2 institutions in 1 country.

Hideki TomiokaDepartment of Clinical Gene Therapy, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, Japan; AnGesMG, Inc., 7-7-15 Saito Bio-Incubator, Ibaraki, Osaka, Japan.
Hironori NakagamiDivision of Vascular Medicine and Epigenetics, Osaka University United Graduate School of Child Development, 2-1 Yamada-oka, Suita, Osaka, Japan.
Akiko TenmaAnGesMG, Inc., 7-7-15 Saito Bio-Incubator, Ibaraki, Osaka, Japan.
Yoshimi SaitoAnGesMG, Inc., 7-7-15 Saito Bio-Incubator, Ibaraki, Osaka, Japan.
Toshihiro KagaAnGesMG, Inc., 7-7-15 Saito Bio-Incubator, Ibaraki, Osaka, Japan.
Toshihide KanamoriAnGesMG, Inc., 7-7-15 Saito Bio-Incubator, Ibaraki, Osaka, Japan.
Nao TamuraAnGesMG, Inc., 7-7-15 Saito Bio-Incubator, Ibaraki, Osaka, Japan.
Kazunori TomonoDivision of Infection Control and Prevention, Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, Japan.
Yasufumi KanedaDivision of Gene Therapy Science, Osaka University Graduate School of Medicine, School of Child Development, 2-1 Yamada-oka, Suita, Osaka, Japan.
Ryuichi MorishitaDepartment of Clinical Gene Therapy, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, Japan.
Anges (Japan) · JPOsaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We developed a novel cationic antimicrobial peptide, AG30/5C, which demonstrates angiogenic properties similar to those of LL-37 or PR39. However, improvement of its stability and cost efficacy are required for clinical application. Therefore, we examined the metabolites of AG30/5C, which provided the further optimized compound, SR-0379. SR-0379 enhanced the proliferation of human dermal fibroblast cells (NHDFs) via the PI3 kinase-Akt-mTOR pathway through integrin-mediated interactions. Furthermore SR-0379 promoted the tube formation of human umbilical vein endothelial cells (HUVECs) in co-culture with NHDFs. This compound also displays antimicrobial activities against a number of bacteria, including drug-resistant microbes and fungi. We evaluated the effect of SR-0379 in two different would-healing models in rats, the full-thickness defects under a diabetic condition and an acutely infected wound with full-thickness defects and inoculation with Staphylococcus aureus. Treatment with SR-0379 significantly accelerated wound healing when compared to fibroblast growth factor 2 (FGF2). The beneficial effects of SR-0379 on wound healing can be explained by enhanced angiogenesis, granulation tissue formation, proliferation of endothelial cells and fibroblasts and antimicrobial activity. These results indicate that SR-0379 may have the potential for drug development in wound repair, even under especially critical colonization conditions.

Indexed as

AnimalsAntimicrobial Cationic PeptidesBacteriaCell ProliferationDisease Models, AnimalEndothelial CellsFibroblast Growth Factor 2FungiHumansMaleMetabolomicsMicrobial Sensitivity TestsPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktRatsSignal TransductionAG30 peptideAntimicrobial Cationic PeptidesFibroblast Growth Factor 2Phosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktSR-0379TOR Serine-Threonine Kinases

Identifiers

PMID24675668
PMCPMC3968008
OpenAlexW1984833729

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.