Evidence map›Paper›PMID 16874361›Full record

ArticleCancer gene therapy2006

Evaluation of adenovirus vectors containing serotype 35 fibers for tumor targeting.

S Ni, A Gaggar, N Di Paolo, Z Y Li, Y Liu, R Strauss, P Sova, J Morihara, Q Feng, N Kiviat and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Auto-expansion ofMolecular therapy. Methods & clinical development · 2024
    Article
  3. Article
  4. Article
  5. Adenovirus as a Vector and Oncolytic Virus.Current issues in molecular biology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. In Vivo Hematopoietic Stem Cell Transduction.Hematology/oncology clinics of North America · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Transient removal of CD46 is safe and increases B-cell depletion by rituximab in CD46 transgenic mice and macaques.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  18. Article
  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 3 institutions in 2 countries.

S NiDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA.
A Gaggar
N Di Paolo
Z Y Li
Y Liu
R Strauss
P Sova
J Morihara
Q Feng
N Kiviat
P Touré
P S Sow
A Lieber
University of Washington Medical Center · USUniversity of Washington · USCheikh Anta Diop University · SN

Funding

ONCOLYTIC ADENOVIRUSES FOR CERVICAL CANCER GENE THERAPYR01CA080192 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 1999 to 2009
$2.0M
NCI NIH HHS CA080192NHLBI NIH HHS HL-00-008PHS HHS HLA078836
6 · The paper itself

Abstract

There is growing evidence from in vitro studies that subgroup B adenoviruses (Ad) can overcome the limitations in safety and tumor transduction efficiency seen with commonly used subgroup C serotype 5-based vectors. In this study, we confirm that the expression level of the B-group Ad receptor, CD46, correlates with the grade of malignancy of cervical cancer in situ. We also demonstrate the in vivo properties of Ad5-based vectors that contain the B-group Ad serotype 35 fiber (Ad5/35) in transgenic mice that express CD46 in a pattern and at a level similar to humans. Upon intravenous and intraperitoneal injection, an Ad5/35 vector did not efficiently transduce normal tissue, but was able to target metastatic or intraperitoneal tumors that express CD46 at levels comparable to human tumors. When an oncolytic Ad5/35-based vector was employed, in both tumor models antitumor effects were observed. Furthermore, injection of Ad5/35 vectors into CD46 transgenic mice caused less innate toxicity than Ad5 vectors. Our data demonstrate that Ad vectors that target CD46 offer advantages over Ad5-based vectors for treatment of cancer.

Indexed as

AdenoviridaeAnimalsCell Line, TumorChemokinesCpG IslandsCytokinesDNA MethylationFemaleGenetic TherapyGenetic VectorsHumansInflammationMembrane Cofactor ProteinMiceMice, Inbred C57BLMice, TransgenicChemokinesCytokinesMembrane Cofactor ProteinRCVRN protein, humanRecoverin

Identifiers

PMID16874361
OpenAlexW2067981408

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.