Evidence map›Paper›PMID 11438831›Full record

ArticleGene therapy2001

Improved gene transfer efficiency to primary and established human pancreatic carcinoma target cells via epidermal growth factor receptor and integrin-targeted adenoviral vectors.

J G Wesseling, P J Bosma, V Krasnykh, E A Kashentseva, J L Blackwell, P N Reynolds, H Li, M Parameshwar, S M Vickers, E M Jaffee and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.3field-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

34 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Vascular density and endothelial cell expression of integrin alpha v beta 3 and E-selectin in murine tumours.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2012
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Current issues and future directions of oncolytic adenoviruses.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Review
  19. 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

13 authors at 5 institutions in 2 countries.

J G WesselingDepartment of Experimental Hepatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
P J Bosma
V Krasnykh
E A Kashentseva
J L Blackwell
P N Reynolds
H Li
M Parameshwar
S M Vickers
E M Jaffee
K Huibregtse
D T Curiel
I Dmitriev
Human Gene Therapy Research Institute · USUniversity of Amsterdam · NLAcademic Medical Center · NLJohns Hopkins Medicine · USUniversity of Alabama at Birmingham · US

Funding

CANCER GENE THERAPY TRAINING PROGRAMT32CA075930 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID TERRY · 1998 to 2008
$1.1M
ADENOVIRAL MEDIATED TARGETED GENE DELIVERYR01CA074242 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID T · 1997 to 2001
$416k
TARGETED VECTORS FOR CYSTIC FIBROSIS GENE THERAPYR01HL050255 · NHLBI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CURIEL, DAVID T · 1992 to 2000
$266k
NOVEL TECHNOLOGIES FOR NONINVASIVE DETECTION, DIAGNOSISN01CO097110 · CO · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID T · 1999 to 2000
$218k
NCI NIH HHS IT32 CA75930NCI NIH HHS N01 CO-97110NCI NIH HHS R01 CA 74242NHLBI NIH HHS R01 HL 50255
6 · The paper itself

Abstract

In this study we analyzed two ways of retargeting of Ad-vectors to human pancreatic carcinoma with the aim of enhancing the gene transfer efficiency. First, we analyzed the expression of the epidermal growth factor receptor (EGFR) on primary, as well as established pancreatic carcinoma cells by flow cytometry which revealed high expression levels of EGFR on the surface of these cells. We showed that EGFR-retargeted entry pathway using a bispecific fusion protein formed by a recombinant soluble form of truncated Coxsackie and Adenovirus Receptor (sCAR) genetically fused with human EGF (sCAR-EGF) redirects them to the EGFR leading to an enhanced gene transfer efficiency to pancreatic carcinoma cells. Since flow cytometry revealed absence of CAR expression, but the presence of at least one of both alphav integrins on the pancreatic carcinoma cells, a second way of targeting was investigated using a genetically modified Ad vector which has an RGD (Arg-Gly-Asp)-containing peptide inserted into the HI-loop of the fiber knob. This RGD targeted Ad (AdlucRGD) revealed efficient CAR-independent infection by allowing binding to cellular integrins resulting in a dramatic enhancement of gene transfer. These findings have direct relevance for Ad-vector based gene therapy strategies for pancreatic carcinoma.

Indexed as

Gene Transfer TechniquesAdenoviridaeErbB ReceptorsGene TargetingGenetic TherapyGenetic VectorsHumansIntegrinsNeoplasm ProteinsPancreatic NeoplasmsReceptors, VitronectinTumor Cells, CulturedErbB Receptorsintegrin alphaVbeta5IntegrinsNeoplasm ProteinsReceptors, Vitronectin

Identifiers

PMID11438831
OpenAlexW2154021432

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.