Evidence map›Paper›PMID 12595887›Full record

ReviewGene therapy2003

Gene therapy progress and prospects: therapeutic angiogenesis for limb and myocardial ischemia.

T A Khan, F W Sellke, R J Laham

Abstract readReview
PubMed Publisher
In one paragraph

Review in Gene therapy, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 122 citations in OpenAlex.

  1. Trial
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  7. Review
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  13. Gene doping: gene delivery for olympic victory.British journal of clinical pharmacology · 2013
    Review
  14. Article
  15. Review
  16. Article
  17. Regenerative therapies for diabetic microangiopathy.Experimental diabetes research · 2012
    Review
  18. Article
  19. Review
  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

3 authors at 1 institution in 1 country.

T A KhanDivision of Cardiothoracic Surgery, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA.
F W Sellke
R J Laham
Harvard University · US

Funding

ZINC STATUS AND T CELL DISORDER IN MILD HUMAN ZINC DEFICIENCYM01RR001032 · NCRR · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ORBAN, TIHAMER · 1985 to 2008
$32.3M
Transcriptional control in cardiac endotheiliumP50HL063609 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI AIRD, WILLIAM C · 2000 to 2004
$8.8M
Effect of Cardioplegia and Cardiopulmonary Bypass on Coronary Microvascular ReactivityR01HL046716 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W · 1997 to 2023
$8.5M
Surgical Intramyocardial Angiogenesis in a Swine Model of Endothelial DysfunctionR01HL069024 · NHLBI · RHODE ISLAND HOSPITAL · PI SELLKE, FRANK W · 2002 to 2011
$3.7M
HMG CoA reductase Inhibitors and cardiopulmonary BypassF32HL069651 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KHAN, TANVEER · 2002 to 2002
$51k
CARDIOPLEGIA AND CORONARY MICROVASCULAR REACTIVITYR29HL046716 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SELLKE, FRANK W · 1992 to 1996
–
NCRR NIH HHS M01-RR01032NHLBI NIH HHS HL46716NHLBI NIH HHS HL63609NHLBI NIH HHS HL69024NHLBI NIH HHS HL69651-01
6 · The paper itself

Abstract

After extensive investigation in preclinical studies and recent clinical trials, gene therapy has been established as a potential method to induce therapeutic angiogenesis in ischemic myocardial and limb disease. Advancements in viral and nonviral vector technology including cell-based gene transfer will continue to improve transgene transmission and expression efficiency. An alternative strategy to the use of transgenes encoding angiogenic growth factors is therapy based on transcription factors such as hypoxia-inducible factor-1alpha (HIF-1alpha) that regulate the expression of multiple angiogenic genes. Further understanding of the underlying biology of neovascularization is needed to determine the ability of growth factors to induce functionally significant angiogenesis in patients with atherosclerotic disease and associated comorbid conditions including endothelial dysfunction, which may inhibit blood vessel growth. The safety and tolerability of therapeutic angiogenesis by gene transfer has been demonstrated in phase I clinical trials. However, limited evidence of efficacy resulted from early phase II studies of angiogenic gene therapy for ischemic myocardial and limb disease. The utility of therapeutic angiogenesis by gene transfer as a treatment option for ischemic cardiovascular disease will be determined by adequately powered, randomized, placebo-controlled phase II and III clinical trials.

Indexed as

AnimalsCoronary DiseaseEndothelial Growth FactorsFibroblast Growth FactorsGene ExpressionGenetic TherapyHumansIntercellular Signaling Peptides and ProteinsLymphokinesModels, AnimalMuscle, SkeletalMyocardiumNeovascularization, PhysiologicPeripheral Vascular DiseasesTransduction, GeneticVascular Endothelial Growth Factor AEndothelial Growth FactorsFibroblast Growth FactorsIntercellular Signaling Peptides and ProteinsLymphokinesVascular Endothelial Growth Factor AVascular Endothelial Growth Factors

Identifiers

PMID12595887
OpenAlexW2147074779

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.