Evidence map›Paper›PMID 15300260›Full record

ArticleNature biotechnology2004

A simple method to cure established tumors by inflammatory killing of normal cells.

Gregory A Daniels, Luis Sanchez-Perez, Rosa Maria Diaz, Timothy Kottke, Jill Thompson, Maoyi Lai, Michael Gough, Mahzuz Karim, Andrew Bushell, Heung Chong and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biotechnology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

58 citing papers in PubMed, 119 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Heat Shock Proteins and HSF1 in Cancer.Frontiers in oncology · 2022
    Review
  10. Heat Shock Proteins in Lymphoma Immunotherapy.Frontiers in immunology · 2021
    Review
  11. Article
  12. The HSP Immune Network in Cancer.Frontiers in immunology · 2021
    Review
  13. Review
  14. Article
  15. RNA-Modified T Cells Mediate Effective Delivery of Immunomodulatory Cytokines to Brain Tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  16. Article
  17. Stimulating Innate Immunity to Enhance Radiation Therapy-Induced Tumor Control.International journal of radiation oncology, biology, physics · 2017
    Review
  18. Targeting Heat Shock Proteins in Cancer: A Promising Therapeutic Approach.International journal of molecular sciences · 2017
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Gregory A DanielsMolecular Medicine Program, Mayo Clinic, Rochester, Minnesota 55905, USA.
Luis Sanchez-Perez
Rosa Maria Diaz
Timothy Kottke
Jill Thompson
Maoyi Lai
Michael Gough
Mahzuz Karim
Andrew Bushell
Heung Chong
Alan Melcher
Kevin Harrington
Richard G Vile
Mayo Clinic · USBalfour Beatty (United Kingdom) · GBJohn Radcliffe Hospital · GBSt George's, University of London · GBSt James's University Hospital · GBUniversity of Oxford · GB

Funding

Utility of serum and Tissue Biomarkers for Predicting Response to Androgen DeprivP50CA091956 · NCI · MAYO CLINIC ROCHESTER · PI TINDALL, DONALD J. · 2001 to 2010
$23.4M
Modulation of Cell Death during Cytotoxic Gene TherapyR01CA094180 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI VILE, RICHARD G · 2002 to 2004
$772k
NCI NIH HHS P50CA91956NCI NIH HHS R01 CA94180
6 · The paper itself

Abstract

We describe a simple technology used to cure an established metastatic disease. Intradermal injection of plasmid DNA encoding a transcriptionally targeted cytotoxic gene, along with hsp70, not only promoted tissue-specific, inflammatory killing of normal melanocytes, but also induced a CD8(+) T-cell-dependent, antigen-specific response in mice that eradicated systemically established B16 tumors. This CD8(+) T cell response was subsequently suppressed in vivo within a few days. The data demonstrate that deliberate destruction of normal tissue can be exploited to generate immunity against a malignant disease originating from that tissue. This approach obviates the need to identify tumor antigens and does not require complex isolation of tumor cells or their derivatives. In addition, it provides a model system for studying the mechanisms underlying the etiology and control of autoimmune diseases. Finally, despite targeting normal tissue, therapy could be separated from development of overt autoimmune symptoms, suggesting that the strategy may be valuable against tumors derived from both non-essential and essential tissue types.

Indexed as

AnimalsAntigensCD8-Positive T-LymphocytesGenetic TherapyImmunity, InnateImmunizationImmunotherapyMelanocytesMelanomaMiceMice, Inbred C57BLMice, NudeSurvival AnalysisThymidine KinaseTreatment OutcomeViral ProteinsAntigensThymidine Kinasethymidine kinase, Canid herpesvirus 1Viral Proteins

Identifiers

PMID15300260
OpenAlexW1976835135

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.