Evidence map›Paper›PMID 15526007›Full record

ArticleGene therapy2005

Mesothelin-mediated targeting of adenoviral vectors for ovarian cancer gene therapy.

M Breidenbach, D T Rein, M Everts, J N Glasgow, M Wang, M J Passineau, R D Alvarez, N Korokhov, D T Curiel

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Rad51 promoter-targeted gene therapy is effective for in vivo visualization and treatment of cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Circulating mesothelin protein and cellular antimesothelin immunity in patients with pancreatic cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2009
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Mesothelin targeted cancer immunotherapy.European journal of cancer (Oxford, England : 1990) · 2008
    Review
  19. Targeting mesothelioma using an infectivity enhanced survivin-conditionally replicative adenoviruses.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2006
    Article
  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

9 authors at 3 institutions in 1 country.

M BreidenbachDivision of Human Gene Therapy, Departments of Medicine, Surgery, Pathology and the Gene Therapy Center, Birmingham, AL 35294-2172, USA.
D T Rein
M Everts
J N Glasgow
M Wang
M J Passineau
R D Alvarez
N Korokhov
D T Curiel
Human Gene Therapy Research Institute · USVector (United States) · USUniversity of Alabama at Birmingham · US

Funding

UAB Rexinoids for Breast Cancer PreventionP50CA089019 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GRIZZLE, WILLIAM E. · 2000 to 2011
$26.0M
Endothelial Gene Delivery for Pulmonary HypertensionR01HL067962 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID TERRY · 2001 to 2004
$1.5M
Enhanced Adenoviral Vectors for Ovarian CancerR01CA090547 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ALVAREZ, RONALD DAVID · 2001 to 2007
$1.3M
In situ therapeutic anti-AB delivery/adenoviral vectorsR01AG021875 · NIA · MAYO CLINIC JACKSONVILLE · PI GOLDE, TODD E. · 2002 to 2004
$707k
NCI NIH HHS P50 CA89019NCI NIH HHS R01 CA090547NHLBI NIH HHS R01 HL67962NIA NIH HHS R01 AG021875
6 · The paper itself

Abstract

Adenoviruses (Ads) are efficient gene transfer vehicles, but Ad-mediated gene therapy for ovarian cancer remains limited in vivo by inefficient and nonspecific gene transfer. Mesothelin (MSLN), a cell surface glycoprotein, is overexpressed in ovarian cancer but not in normal tissues except mesothelial cells. Therefore, MSLN is an attractive candidate for transcriptional and transductional targeting in the context of ovarian cancer gene therapy. We evaluated the expression of MSLN mRNA and MSLN surface protein in ovarian cancer cells. Ads containing the MSLN promoter driving reporter gene expression were created and tested in ovarian cancer cell lines and purified ovarian cancer cells isolated from patients. To evaluate transductional targeting, we used an Ad vector containing an Fc-binding domain within the fiber protein, which served as a docking domain for binding with anti-MSLN immunoglobulins. Both RT-PCR and flow cytometry revealed high MSLN gene and protein expression in ovarian cancer cells. The MSLN promoter was activated in ovarian cancer cells, but showed significantly reduced activity in normal control cells. Transductional targeting of Ads via anti-MSLN antibody increased transgene expression in ovarian cancer cells. This report describes the use of MSLN for transcriptional as well as transductional targeting strategies for ovarian cancer gene therapy.

Indexed as

Promoter Regions, GeneticAdenoviridaeCell LineCell Line, TumorFemaleGene ExpressionGene TargetingGenetic TherapyGenetic VectorsGPI-Linked ProteinsHumansMembrane GlycoproteinsMesothelinOvarian NeoplasmsRNA, MessengerTransduction, GeneticGPI-Linked ProteinsMembrane GlycoproteinsMesothelinMSLN protein, humanRNA, Messenger

Identifiers

PMID15526007
OpenAlexW2006944864

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.