Evidence map›Paper›PMID 22850679›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2012

Inflammation, apoptosis, and necrosis induced by neoadjuvant fas ligand gene therapy improves survival of dogs with spontaneous bone cancer.

Jaime F Modiano, Donald Bellgrau, Gary R Cutter, Susan E Lana, Nicole P Ehrhart, Ej Ehrhart, Vicki L Wilke, J Brad Charles, Sibyl Munson, Milcah C Scott and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Recent and current clinical trials in canine appendicular osteosarcoma.The Canadian veterinary journal = La revue veterinaire canadienne · 2020
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Clonal cooperativity in heterogenous cancers.Seminars in cell & developmental biology · 2017
    Review
  14. Article
  15. Defining the Value of a Comparative Approach to Cancer Drug Development.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Review
  16. Review
  17. 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

14 authors at 8 institutions in 1 country.

Jaime F ModianoApopLogic Pharmaceuticals, Aurora, CO, USA. modiano@umn.edu
Donald Bellgrau
Gary R Cutter
Susan E Lana
Nicole P Ehrhart
Ej Ehrhart
Vicki L Wilke
J Brad Charles
Sibyl Munson
Milcah C Scott
John Pozniak
Cathy S Carlson
Jerome Schaack
Richard C Duke
Colorado State University · USUniversity of Minnesota · USApoplogic Pharmaceuticals (United States) · USNational Jewish Health · USUniversity of Alabama at Birmingham · USUniversity of Colorado Cancer Center · USUniversity of Colorado Denver · USUniversity of Minnesota Medical Center · US

Funding

Provoking anti-tumor immune responses with Fas ligandR43CA119840 · NCI · APOPLOGIC PHARMACEUTICALS, INC. · PI BELLGRAU, DONALD · 2006 to 2007
$665k
NCI NIH HHS 1R43 CA119840NCI NIH HHS R43 CA119840
6 · The paper itself

Abstract

Fas ligand (FasL) gene therapy for cancer has shown promise in rodents; however, its efficacy in higher mammals remains unknown. Here, we used intratumoral FasL gene therapy delivered in an adenovirus vector (Ad-FasL) as neoadjuvant to standard of care in 56 dogs with osteosarcoma. Tumors from treated dogs had greater inflammation, necrosis, apoptosis, and fibrosis at day 10 (amputation) compared to pretreatment biopsies or to tumors from dogs that did not receive Ad-FasL. Survival improvement was apparent in dogs with inflammation or lymphocyte-infiltration scores >1 (in a 3-point scale), as well as in dogs that had apoptosis scores in the top 50th percentile (determined by cleaved caspase-3). Survival was no different than that expected from standard of care alone in dogs with inflammation scores ≤1 or apoptosis scores in the bottom 50th percentile. Reduced Fas expression by tumor cells was associated with prognostically advantageous inflammation, and this was seen only in dogs that received Ad-FasL. Together, the data suggest that Ad-FasL gene therapy improves survival in a subset of large animals with naturally occurring tumors, and that at least in some tumor types like osteosarcoma, it is most effective when tumor cells fail to express Fas.

Indexed as

AnimalsApoptosisBone NeoplasmsDogsFas Ligand ProteinGenetic TherapyNecrosisOsteosarcomaFas Ligand Protein

Identifiers

PMID22850679
PMCPMC3519983
OpenAlexW2032531003

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.