Evidence map›Paper›PMID 12719707›Full record

ArticleCancer gene therapy2003

Replication of an integrin targeted conditionally replicating adenovirus on primary ovarian cancer spheroids.

John T Lam, Gerd J Bauerschmitz, Anna Kanerva, Shannon D Barker, J Michael Straughn, Minghui Wang, Mack N Barnes, Jerry L Blackwell, Gene P Siegal, Ronald D Alvarez and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-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

9 citing papers in PubMed, 27 citations in OpenAlex.

  1. Mesenchymal stromal cell delivery of oncolytic immunotherapy improves CAR-T cell antitumor activity.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Targeted and shielded adenovectors for cancer therapy.Cancer immunology, immunotherapy : CII · 2006
    Review
  8. Article
  9. 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

12 authors at 1 institution in 2 countries.

John T LamDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Gerd J Bauerschmitz
Anna Kanerva
Shannon D Barker
J Michael Straughn
Minghui Wang
Mack N Barnes
Jerry L Blackwell
Gene P Siegal
Ronald D Alvarez
David T Curiel
Akseli Hemminki
University 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
Targeted immunotherapy programP50CA083591 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PARTRIDGE, EDWARD E · 1999 to 2005
$9.6M
HEMATOPOIETIC COMMITMENT: MOLECULAR MECHANISMSR01HL063736 · NHLBI · WASHINGTON UNIVERSITY · PI CHOI, KYUNGHEE · 2000 to 2016
$5.6M
Enhanced CRAd for Pancreatic CancerR01CA094084 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2002 to 2013
$2.7M
REPLICATIVE ADENOVIRUSES WITH ENHANCED INFECTIVITYR01CA083821 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID TERRY · 2000 to 2008
$1.9M
CANCER GENE THERAPY TRAINING PROGRAMT32CA075930 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURIEL, DAVID TERRY · 1998 to 2008
$1.1M
Canine model for evaluating CRAD efficacyR01CA093796 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SIEGAL, GENE P · 2002 to 2005
$1.1M
NEUROFIBROMATOSIS 2 TUMOR SUPPRESSOR GENE HOMOLOG INK01CA074243 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI GOBEL, VERENA · 1997 to 2001
$313k
NCI NIH HHS CA74243NCI NIH HHS CA93796NCI NIH HHS IT32 CA75930NCI NIH HHS P50 CA83591NCI NIH HHS P50 CA89019NCI NIH HHS R01 CA83821NCI NIH HHS R01 CA94084NCI NIH HHS T32 CA75930NHLBI NIH HHS HL63736
6 · The paper itself

Abstract

Replication competent viruses hold promise for treatment of advanced cancers resistant to available therapeutic modalities. Although preliminary clinical results have substantiated their efficacy, preclinical development of these novel approaches is limited by assay substrates. The evaluation of candidate agents could be confounded by differences between primary tumor cells and tumor cell lines, as discordance in the levels of surface receptors relevant for viral entry has been reported. Since primary tumor cells are difficult to analyze ex vivo for longitudinal observation of virus replication, we developed three-dimensional aggregates or spheroids of unpassaged and purified ovarian cancer cells as a means for prolonging primary tumor cell viability and as a three-dimensional in vitro model for replicative viral infection. Ovarian cancer cells purified from ascites samples were sustained for 30 days while retaining the infection profile with tropism modified and unmodified adenoviruses (Ads). Cell line and primary cell spheroids were used to quantitate the replication and oncolytic potency of replicative Ads in preclinical testing for human ovarian cancer trials. Therefore, spheroids provide a method to sustain purified unpassaged primary ovarian cancer cells for extended periods and to allow evaluation of replicative viruses in a three-dimensional model.

Indexed as

Virus ReplicationAdenoviridaeAscitesFemaleGenetic TherapyGenetic VectorsGene Transfer TechniquesHumansIntegrinsOligopeptidesOvarian NeoplasmsSpheroids, CellularTumor Cells, Culturedarginyl-glycyl-aspartic acidIntegrinsOligopeptides

Identifiers

PMID12719707
OpenAlexW2074520970

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.