Evidence map›Paper›PMID 22391130›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2012

Therapeutic angiogenesis due to balanced single-vector delivery of VEGF and PDGF-BB.

Andrea Banfi, Georges von Degenfeld, Roberto Gianni-Barrera, Silvia Reginato, Milton J Merchant, Donald M McDonald, Helen M Blau

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

51 citing papers in PubMed, 101 citations in OpenAlex.

  1. Review
  2. Review
  3. Pathophysiology of chronic subdural hematoma-new insights.Therapeutic advances in neurological disorders · 2026
    Review
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  7. Review
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  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Vasculogenic gene therapy: No role for revitalization of structural bone allografts.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  16. Article
  17. Review
  18. Targeting tumor vascularization: promising strategies for vascular normalization.Journal of cancer research and clinical oncology · 2021
    Review
  19. Review
  20. 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

7 authors at 4 institutions in 3 countries.

Andrea BanfiBaxter Laboratory for Stem Cell Biology, Institute for Regenerative Medicine and Stem Cell Biology, Department of Microbiology and Immunology, Stanford University, Stanford, California 34305-5175, USA. abanfi@uhbs.ch
Georges von Degenfeld
Roberto Gianni-Barrera
Silvia Reginato
Milton J Merchant
Donald M McDonald
Helen M Blau
Institute for Stem Cell Biology and Regenerative Medicine · INUniversity Hospital of Basel · CHBaxter (United States) · USUniversity of California, San Francisco · US

Funding

Tools for Analysis of Airway InflammationP01HL024136 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 1985 to 2014
$23.3M
ENDOTHELIAL PERMEABILITY IN AIRWAY ANGIOGENESISR01HL059157 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCDONALD, DONALD M · 1998 to 2015
$5.5M
Stem Cells for Brain and BrawnR01AG020961 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2002 to 2019
$5.0M
ACTIVATORS OF MUSCLE GENESR01AG009521 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 1990 to 2014
$4.7M
Telomere extension using nucleoside-modified mRNA and exosomes as a novel therapeR01AR063963 · NIAMS · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2012 to 2016
$4.3M
MRI MONITORING OF ANGIOGENESIS INHIBITIONR01CA082923 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BRASCH, ROBERT CHARLES · 1999 to 2008
$2.9M
Regulation of Hematopoietic Stem Cell Fate in Bioengineered NichesR01HL096113 · NHLBI · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2009 to 2013
$2.7M
ACTIVATORS OF HUMAN MUSCLE GENESR37AG009521 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 1995 to 2004
$2.3M
Regulator of Adult Stem Cell FateR01AG024987 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2004 to 2008
$1.7M
DELIVERY AND REGULATION OF ANGIOGENIC GENESR01HL065572 · NHLBI · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2000 to 2003
$1.5M
Safe, Rapid Telomere Extension to Prevent and Treat HypertensionR21AG044815 · NIA · STANFORD UNIVERSITY · PI BLAU, HELEN M · 2013 to 2014
$434k
NCI NIH HHS CA-082923NCI NIH HHS R01 CA082923NHLBI NIH HHS HL-065572NHLBI NIH HHS HL-24136NHLBI NIH HHS HL-59157NHLBI NIH HHS P01 HL024136NHLBI NIH HHS R01 HL059157NHLBI NIH HHS R01 HL065572NHLBI NIH HHS R01 HL096113NIAMS NIH HHS R01 AR063963NIA NIH HHS AG-009521NIA NIH HHS AG-020961NIA NIH HHS AG-024987NIA NIH HHS R01 AG009521NIA NIH HHS R01 AG020961NIA NIH HHS R01 AG024987NIA NIH HHS R21 AG044815NIA NIH HHS R37 AG009521
6 · The paper itself

Abstract

Therapeutic angiogenesis by delivery of vascular growth factors is an attractive strategy for treating debilitating occlusive vascular diseases, yet clinical trials have thus far failed to show efficacy. As a result, limb amputation remains a common outcome for muscle ischemia due to severe atherosclerotic disease, with an overall incidence of 100 per million people in the United States per year. A challenge has been that the angiogenic master regulator vascular endothelial growth factor (VEGF) induces dysfunctional vessels, if expressed outside of a narrow dosage window. We tested the hypothesis that codelivery of platelet-derived growth factor-BB (PDGF-BB), which recruits pericytes, could induce normal angiogenesis in skeletal muscle irrespective of VEGF levels. Coexpression of VEGF and PDGF-BB encoded by separate vectors in different cells or in the same cells only partially corrected aberrant angiogenesis. In marked contrast, coexpression of both factors in every cell at a fixed relative level via a single bicistronic vector led to robust, uniformly normal angiogenesis, even when VEGF expression was high and heterogeneous. Notably, in an ischemic hindlimb model, single-vector expression led to efficient growth of collateral arteries, revascularization, increased blood flow, and reduced tissue damage. Furthermore, these results were confirmed in a clinically applicable gene therapy approach by adenoviral-mediated delivery of the bicistronic vector. We conclude that coordinated expression of VEGF and PDGF-BB via a single vector constitutes a novel strategy for harnessing the potency of VEGF to induce safe and efficacious angiogenesis.

Indexed as

AdenoviridaeAnimalsBecaplerminGenetic TherapyGenetic VectorsGene Transfer TechniquesHEK293 CellsHindlimbHumansMaleMiceMice, SCIDMuscle, SkeletalNeovascularization, PhysiologicPlatelet-Derived Growth FactorProto-Oncogene Proteins c-sisBecaplerminPlatelet-Derived Growth FactorProto-Oncogene Proteins c-sisVascular Endothelial Growth Factor A

Identifiers

PMID22391130
PMCPMC3360154
OpenAlexW2135293820

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.