Evidence map›Paper›PMID 17020944›Full record

ArticleJournal of virology2006

A new group B adenovirus receptor is expressed at high levels on human stem and tumor cells.

Sebastian Tuve, Hongjie Wang, Carol Ware, Ying Liu, Anuj Gaggar, Kathrin Bernt, Dmitry Shayakhmetov, Zongyi Li, Robert Strauss, Daniel Stone and 1 more

Abstract readComparative Study
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
–field-weighted citation impact
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

76 citing papers in PubMed.

  1. Treatment of cancer patients with a serotype 5/3 chimeric oncolytic adenovirus expressing GMCSF.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Trial
  2. Article
  3. Review
  4. Review
  5. Safe and efficientMolecular therapy. Methods & clinical development · 2022
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Gene Therapy Leaves a Vicious Cycle.Frontiers in oncology · 2019
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

16 more citing papers are in PubMed but not listed here.

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

11 authors.

Sebastian TuveDivision of Medical Genetics, Box 357720, University of Washington, Seattle, WA 98195, USA.
Hongjie Wang
Carol Ware
Ying Liu
Anuj Gaggar
Kathrin Bernt
Dmitry Shayakhmetov
Zongyi Li
Robert Strauss
Daniel Stone
André Lieber

Funding

VECTOR CONSTRUCTIONS FOR GENE THERAPY OF SICKLE CELL DISEASEP01HL053750 · NHLBI · UNIVERSITY OF WASHINGTON · PI RUSSELL, DAVID W · 1994 to 2014
$30.4M
UW/FHCRC Exploratory Center for Human ES Cell ResearchP20GM069983 · NIGMS · UNIVERSITY OF WASHINGTON · PI BLAU, C. ANTHONY · 2003 to 2006
$3.0M
ONCOLYTIC ADENOVIRUSES FOR CERVICAL CANCER GENE THERAPYR01CA080192 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 1999 to 2009
$2.0M
NCI NIH HHS CA080192NCI NIH HHS R01 CA080192NHLBI NIH HHS HL53750NHLBI NIH HHS P01 HL053750NIGMS NIH HHS IP20 GM69983NIGMS NIH HHS P20 GM069983PHS HHS HLA078836
6 · The paper itself

Abstract

CD46 is used by human group B adenoviruses (Ads) as a high-affinity attachment receptor. Here we show evidence that several group B Ads utilize an additional receptor for infection of human cells, which is different from CD46. We tentatively named this receptor receptor X. Competition studies with unlabeled and labeled Ads, recombinant Ad fiber knobs, and soluble CD46 and CD46 antibodies revealed three different subgroups of group B Ads, in terms of their receptor usage. Group I (Ad16, -21, -35, and -50) nearly exclusively uses CD46. Group II (Ad3, -7p, and -14) utilizes receptor X and not CD46. Group III (Ad11p) uses both CD46 and the alternative receptor X. Interaction of group II and III Ads with receptor X occurs via the fiber knob. Receptor X is an abundantly expressed glycoprotein that interacts with group II and III Ads at relatively low affinity in a Ca(2+)-dependent manner. This receptor is expressed at high levels on human mesenchymal and undifferentiated embryonic stem cells, as well as on human cancer cell lines. These findings have practical implications for stem cell and gene therapy.

Indexed as

Adenoviruses, HumanAlkaline PhosphataseAntibodies, Viralbeta-GalactosidaseCell Line, TumorEmbryonic Stem CellsFlow CytometryHumansMembrane Cofactor ProteinReceptors, VirusRNA, Small InterferingAlkaline PhosphataseAntibodies, Viralbeta-GalactosidaseCD46 protein, humanMembrane Cofactor ProteinReceptors, VirusRNA, Small Interfering

Identifiers

PMID17020944
PMCPMC1676274

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.