Evidence map›Paper›PMID 16707084›Full record

ArticleAnalytical biochemistry2006

A rapid and efficient method for purification of recombinant adenovirus with arginine-glycine-aspartic acid-modified fibers.

Henry H Peng, Shuhong Wu, John J Davis, Li Wang, Jack A Roth, Frank C Marini, Bingliang Fang

Open access · greenAbstract read
In one paragraph

Article in Analytical biochemistry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Chromatographic Purification of Viral Vectors for Gene Therapy Applications.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  5. Stable expression of shRNA for the control of recombinant adenovirus replication.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2023
    Article
  6. Article
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  9. Review
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  11. Combination of epidural electrical stimulation withNeural regeneration research · 2021
    Article
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  13. Article
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  15. Article
  16. p19Arf sensitizes B16 melanoma cells to interferon-β delivered via mesenchymal stem cells in vitro.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  17. Article
  18. Article
  19. Reestablishment of p53/Arf and interferon-Cell death discovery · 2017
    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

7 authors at 2 institutions in 1 country.

Henry H PengDepartment of Thoracic and Cardiovascular Surgery, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.
Shuhong Wu
John J Davis
Li Wang
Jack A Roth
Frank C Marini
Bingliang Fang
The University of Texas MD Anderson Cancer Center · USThoracic Surgery Foundation · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
Strategies for Cell Death Manipulation in CancerP01CA078778 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI ROTH, JACK · 1999 to 2003
$4.4M
Oncolytic adenovector-mediated TRAIL gene therapy for cancersR01CA092487 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FANG, BINGLIANG · 2002 to 2011
$2.4M
Expression of Proapoptotic Genes for Cancer TherapyR01CA098582 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FANG, BINGLIANG · 2003 to 2006
$1.3M
NCI NIH HHS 2P50-CA70907NCI NIH HHS CA 16672NCI NIH HHS P01 CA078778NCI NIH HHS P01 CA78778-01A1NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907NCI NIH HHS R01 CA092487NCI NIH HHS R01 CA 092487-01A1NCI NIH HHS R01 CA098582NCI NIH HHS R01 CA098582-01A1
6 · The paper itself

Abstract

Recombinant adenoviral vectors (adenovectors) have been subject to various genetic modifications to improve their transduction efficiency and targeting capacity. Production and purification of adenovectors with modified capsid proteins can be problematic using conventional two-cycle CsCl gradient ultracentrifugation. We have developed a new method for purifying recombinant adenovectors in two steps: iodixanol discontinuous density gradient ultracentrifugation and size exclusion column chromatography. The purity and infectious activity of adenovectors isolated by the two methods were comparable. The new method yielded three to four times more adenovectors with arginine-glycine-aspartic acid (RGD)-modified fiber proteins than did the conventional CsCl method. For other fiber-modified and wild-type adenovectors, the yields of the two methods were comparable. Thus, the iodixanol-based method can be used not only to improve the production of RGD-modified adenovectors but also to purify adenovectors with or without fiber modifications. Moreover, the whole procedure can be completed in 3h. Therefore, this method is rapid and efficient for production of recombination adenovectors, especially those with RGD-modified fibers.

Indexed as

AdenoviridaeCells, CulturedCentrifugation, Density GradientChromatography, GelContrast MediaGenetic VectorsHumansOligopeptidesTriiodobenzoic Acidsarginyl-glycyl-aspartic acidContrast MediaiodixanolOligopeptidesTriiodobenzoic Acids

Identifiers

PMID16707084
PMCPMC1475777
OpenAlexW2084579230

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.