Evidence map›Paper›PMID 13678451›Full record

ArticleTissue engineering2003

Platelet-derived growth factor gene delivery stimulates ex vivo gingival repair.

Orasa Anusaksathien, Sarah A Webb, Qi-Ming Jin, William V Giannobile

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Gene therapy in periodontics.Journal of Indian Society of Periodontology · 2013
    Article
  10. Article
  11. Review
  12. Article
  13. Gene therapy and its implications in Periodontics.Journal of Indian Society of Periodontology · 2009
    Article
  14. Article
  15. Craniofacial tissue engineering by stem cells.Journal of dental research · 2006
    Review
  16. Review
  17. Nano-fibrous scaffold for controlled delivery of recombinant human PDGF-BB.Journal of controlled release : official journal of the Controlled Release Society · 2006
    Article
  18. Gene therapeutics for periodontal regenerative medicine.Dental clinics of North America · 2006
    Review
  19. Current concepts in periodontal bioengineering.Orthodontics & craniofacial research · 2005
    Review
  20. Engineering of tooth-supporting structures by delivery of PDGF gene therapy vectors.Molecular therapy : the journal of the American Society of Gene Therapy · 2004
    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

4 authors at 1 institution in 1 country.

Orasa AnusaksathienCenter for Craniofacial Regeneration and Department of Periodontics, Prevention, and Geriatrics, School of Dentistry, University of Michigan, Ann Arbor, Michigan 48109-1078, USA.
Sarah A Webb
Qi-Ming Jin
William V Giannobile
University of Michigan–Ann Arbor · US

Funding

GENE THERAPY FOR RECONSTRUCTING PERIODONTAL TISSUESR01DE013397 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GIANNOBILE, WILLIAM V · 2000 to 2014
$4.0M
PDGF-MEDIATED GENE TRANSFER &PERIODONTAL WOUND HEALINGR29DE011960 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GIANNOBILE, WILLIAM V · 1997 to 2001
$239k
NIDCR NIH HHS DE 013397NIDCR NIH HHS DE 11960NIDCR NIH HHS R01 DE013397NIDCR NIH HHS R29 DE011960
6 · The paper itself

Abstract

Destruction of tooth support due to the chronic inflammatory disease periodontitis is a major cause of tooth loss. There are limitations with available treatment options to tissue engineer soft tissue periodontal defects. The exogenous application of growth factors (GFs) such as platelet-derived growth factor (PDGF) has shown promise to enhance oral and periodontal tissue regeneration. However, the topical administration of GFs has not led to clinically significant improvements in tissue regeneration because of problems in maintaining therapeutic protein levels at the defect site. The utilization of PDGF gene transfer may circumvent many of the limitations with protein delivery to soft tissue wounds. The objective of this study was to test the effect of PDGF-A and PDGF-B gene transfer to human gingival fibroblasts (HGFs) on ex vivo repair in three-dimensional collagen lattices. HGFs were transduced with adenovirus encoding PDGF-A and PDGF-B genes. Defect fill of bilayer collagen gels was measured by image analysis of cell repopulation into the gingival defects. The modulation of gene expression at the defect site and periphery was measured by RT-PCR during a 10-day time course after gene delivery. The results demonstrated that PDGF-B gene transfer stimulated potent (>4-fold) increases in cell repopulation and defect fill above that of PDGF-A and corresponding controls. PDGF-A and PDGF-B gene expression was maintained for at least 10 days. PDGF gene transfer upregulated the expression of phosphatidylinosital 3-kinase and integrin alpha5 subunit at 5 days after adenovirus transduction. These results suggest that PDGF gene transfer has potential for periodontal soft tissue-engineering applications.

Indexed as

Gene Transfer TechniquesAdenoviridaeCollagenFibroblastsGenetic VectorsGingivaHumansPlatelet-Derived Growth FactorProto-Oncogene Proteins c-sisRegenerationTime FactorsTissue EngineeringCollagenPlatelet-Derived Growth Factorplatelet-derived growth factor AProto-Oncogene Proteins c-sis

Identifiers

PMID13678451
PMCPMC2586961
OpenAlexW2029137365

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.