Evidence map›Paper›PMID 23097312›Full record

ArticleJournal of cellular biochemistry2013

Growth factor transgenes interactively regulate articular chondrocytes.

Shuiliang Shi, Scott Mercer, George J Eckert, Stephen B Trippel

Abstract read
In one paragraph

Article in Journal of cellular biochemistry, 2013. 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
2.8field-weighted citation impact, top 10% 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, 38 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Harnessing Growth Factor Interactions to Optimize Articular Cartilage Repair.Advances in experimental medicine and biology · 2023
    Review
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  19. Endogenous versus exogenous growth factor regulation of articular chondrocytes.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2014
    Article
  20. 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 2 institutions in 1 country.

Shuiliang ShiDepartment of Orthopaedic Surgery, Indiana University School of Medicine, Indianapolis, Indiana 46202-5111.
Scott Mercer
George J Eckert
Stephen B Trippel
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · US

Funding

Gene Transfer Treatment of Articular Cartilage DamageR01AR047702 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TRIPPEL, STEPHEN B. · 2002 to 2014
$3.8M
Selection of Therapeutic Agents for Articular Cartilage RepairI01BX000447 · VA · RLR VA MEDICAL CENTER · PI TRIPPEL, STEPHEN B. · 2009 to 2013
–
BLRD VA I01 BX000447NIAMS NIH HHS AR047702NIAMS NIH HHS R01 AR047702
6 · The paper itself

Abstract

Adult articular chondrocytes lack an effective repair response to correct damage from injury or osteoarthritis. Polypeptide growth factors that stimulate articular chondrocyte proliferation and cartilage matrix synthesis may augment this response. Gene transfer is a promising approach to delivering such factors. Multiple growth factor genes regulate these cell functions, but multiple growth factor gene transfer remains unexplored. We tested the hypothesis that multiple growth factor gene transfer selectively modulates articular chondrocyte proliferation and matrix synthesis. We tested the hypothesis by delivering combinations of the transgenes encoding insulin-like growth factor I (IGF-I), fibroblast growth factor-2 (FGF-2), transforming growth factor beta1 (TGF-β1), bone morphogenetic protein-2 (BMP-2), and bone morphogenetic protien-7 (BMP-7) to articular chondrocytes and measured changes in the production of DNA, glycosaminoglycan, and collagen. The transgenes differentially regulated all these chondrocyte activities. In concert, the transgenes interacted to generate widely divergent responses from the cells. These interactions ranged from inhibitory to synergistic. The transgene pair encoding IGF-I and FGF-2 maximized cell proliferation. The three-transgene group encoding IGF-I, BMP-2, and BMP-7 maximized matrix production and also optimized the balance between cell proliferation and matrix production. These data demonstrate an approach to articular chondrocyte regulation that may be tailored to stimulate specific cell functions, and suggest that certain growth factor gene combinations have potential value for cell-based articular cartilage repair.

Indexed as

AnimalsBone Morphogenetic Protein 2Bone Morphogenetic Protein 7Cartilage, ArticularCattleCell DifferentiationCell ProliferationCells, CulturedChondrocytesCollagenFibroblast Growth FactorsGene Expression RegulationGenetic VectorsHumansInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsBMP2 protein, humanBMP7 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 7CollagenFGF20 protein, humanFibroblast Growth FactorsInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsProteoglycansTransforming Growth Factor beta1

Identifiers

PMID23097312
PMCPMC3994886
OpenAlexW2152834578

What OpenQuestion holds

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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.