Evidence map›Paper›PMID 19741731›Full record

ArticleGene therapy2010

Therapeutic potential of genetically modified adult stem cells for osteopenia.

S Kumar, T R Nagy, S Ponnazhagan

Open access · bronzeAbstract read
In one paragraph

Article in Gene therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Gene therapy in India: a focus.Journal of biosciences · 2014
    Review
  7. Article
  8. Mesenchymal stem cells as a novel vaccine platform.Frontiers in cellular and infection microbiology · 2012
    Article
  9. Article
  10. Review
  11. Article
  12. Chemistry and material science at the cell surface.Materials today (Kidlington, England) · 2010
    Article
  13. 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

3 authors at 1 institution in 1 country.

S KumarDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294-0007, USA.
T R Nagy
S Ponnazhagan
University of Alabama at Birmingham · US

Funding

Gene-Engineered and Targeted Stem Cell Therapy for MyelomaR01CA133737 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PONNAZHAGAN, SELVARANGAN · 2009 to 2013
$1.5M
AAV-Mediated Gene Therapy for Metabolic Bone DiseaseR01AR050251 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PONNAZHAGAN, SELVARANGAN · 2005 to 2009
$1.4M
NCI NIH HHS CA133737NCI NIH HHS R01 CA133737NIAMS NIH HHS AR50251NIAMS NIH HHS R01 AR050251
6 · The paper itself

Abstract

Adult stem cells have therapeutic potential because of their intrinsic capacity for self-renewal, especially for bone regeneration. The present study shows the utility of ex vivo modified mesenchymal stem cells (MSC) to enhance bone density in an immunocompetent mouse model of osteopenia. MSC were transduced ex vivo with a recombinant adeno-associated virus 2 (rAAV2) expressing bone morphogenetic protein 2 (BMP2) under the transcriptional control of collagen type-1alpha promoter. To enrich bone homing in vivo, we further modified the cells to transiently express the mouse alpha4 integrin. The modified MSC were systemically administered to ovariectomized, female C57BL/6 mice. Effects of the therapy were determined by dual-energy X-ray absorptiometry, 3D micro-CT, histology and immunohistochemistry for up to 6 months. Results indicated that mice transplanted with MSC expressing BMP2 showed significant increase in bone mineral density and bone mineral content (P < 0.001) with relatively better proliferative capabilities of bone marrow stromal cells and higher osteocompetent pool of cells compared to control animals. Micro-CT analysis of femora and other bone histomorphometric analyses indicated more trabecular bone following MSC-BMP2 therapy. Results obtained by transplanting genetically modified MSC from green fluorescent protein transgenic mouse suggested that production of BMP2 from transplanted MSC also influenced the mobilization of endogenous progenitors for new bone formation.

Indexed as

Gene Transfer TechniquesMesenchymal Stem Cell TransplantationAnimalsBone DensityBone Diseases, MetabolicBone Morphogenetic Protein 2Collagen Type IDependovirusFemaleHumansIntegrin alpha4Mesenchymal Stem CellsMiceMice, Inbred C57BLTransduction, GeneticBone Morphogenetic Protein 2Collagen Type IIntegrin alpha4

Identifiers

PMID19741731
PMCPMC2941444
OpenAlexW2105709419

What OpenQuestion holds

Textmetadata
LicenceTDM
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.