Evidence map›Paper›PMID 16424031›Full record

ArticleCancer research2006

Effect of adenovirus-mediated heat shock protein expression and oncolysis in combination with low-dose cyclophosphamide treatment on antitumor immune responses.

Nelson C Di Paolo, Sebastian Tuve, Shaoheng Ni, Karl Erik Hellström, Ingegerd Hellström, André Lieber

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Immunological Mechanisms of Low and Ultra-Low Dose Cancer Chemotherapy.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2015
    Article
  5. DC targeting DNA vaccines induce protective and therapeutic antitumor immunity in mice.International journal of clinical and experimental medicine · 2015
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Intelligent design: combination therapy with oncolytic viruses.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Review
  17. Administration of cyclophosphamide changes the immune profile of tumor-bearing mice.Journal of immunotherapy (Hagerstown, Md. : 1997) · 2010
    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

6 authors at 1 institution in 1 country.

Nelson C Di PaoloDivision of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA.
Sebastian Tuve
Shaoheng Ni
Karl Erik Hellström
Ingegerd Hellström
André Lieber
University of Washington · US

Funding

ONCOLYTIC ADENOVIRUSES FOR CERVICAL CANCER GENE THERAPYR01CA080192 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 1999 to 2009
$2.0M
Melanoma vaccinesR01CA112073 · NCI · UNIVERSITY OF WASHINGTON · PI HELLSTROM, KARL ERIK · 2005 to 2007
$701k
Gene Therapy for HPV-Associated MalignanciesR21CA109081 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2005 to 2006
$300k
NCI NIH HHS R01 CA 080192NCI NIH HHS R01 CA 112073NCI NIH HHS R21 CA 109081NCI NIH HHS R21 CA109081
6 · The paper itself

Abstract

Heat shock proteins such as gp96 have the ability to chaperone peptides and activate antigen-presenting cells. In this study, we tested whether adenovirus-mediated overexpression of secreted or membrane-associated forms of gp96 in tumor cells would stimulate an antitumor immune response. Studies were carried out in C57Bl/6 mice bearing aggressively growing s.c. tumors derived from syngeneic TC-1 cells, a cell line that expresses HPV16 E6 and E7 proteins. We found that secreted gp96 can induce protective and therapeutic antitumor immune responses. Our data also indicate that the antitumor effect of sgp96 expression seems to be limited by the induction of suppressive regulatory T cells (Treg). TC-1 tumor transplantation increased the number of splenic and tumor-infiltrating Tregs. Importantly, treatment of mice with low-dose cyclophosphamide decreased the number of Tregs and enhanced the immunostimulatory effect of sgp96 expression. We also tested whether an oncolytic vector (Ad.IR-E1A/TRAIL), that is able to induce tumor cell apoptosis and, potentially, release cryptic tumor epitopes in immunogenic form, could stimulate antitumor immune responses. Although tumor cells infected ex vivo with Ad.IR-E1A/TRAIL had no antitumor effect when used as a vaccine alone, the additional treatment with low-dose cyclophosphamide resulted in the elimination of pre-established tumors. This study gives a rationale for testing approaches that suppress Tregs in combination with oncolytic or immunostimulatory vectors.

Indexed as

AdenoviridaeAnimalsAntigen-Presenting CellsAntineoplastic Agents, AlkylatingCancer VaccinesCyclophosphamideDose-Response Relationship, DrugGenetic VectorsHeat-Shock ProteinsHuman papillomavirus 16HumansMembrane GlycoproteinsMiceMice, Inbred C57BLNeoplasmsOncogene Proteins, ViralAntineoplastic Agents, AlkylatingCancer VaccinesCyclophosphamideE6 protein, Human papillomavirus type 16endoplasminHeat-Shock ProteinsMembrane GlycoproteinsOncogene Proteins, ViralRepressor Proteins

Identifiers

PMID16424031
PMCPMC1360184
OpenAlexW2097494460

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.