Evidence map›Paper›PMID 17726452›Full record

ArticleProstate cancer and prostatic diseases2008

Combining gene and immunotherapy for prostate cancer.

J G Young, N K Green, V Mautner, P F Searle, L S Young, N D James

Abstract readEvaluation Study
PubMed Publisher
In one paragraph

Article in Prostate cancer and prostatic diseases, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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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 2 institutions in 1 country.

J G YoungCancer Research UK Institute for Cancer Studies, University of Birmingham, Edgbaston, Birmingham, UK.
N K Green
V Mautner
P F Searle
L S Young
N D James
University of Birmingham · GBCancer Research UK · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

The nitroreductase (NR)/CB1954 enzyme prodrug system has given promising results in pre-clinical studies and is currently being assessed in phase I and II clinical trials in prostate cancer. Enhanced cell killing by apparent immune-mediated mechanisms has been shown in pancreatic and colorectal cancer models, by co-expressing murine granulocyte macrophage colony-stimulating factor (GM-CSF) with NR in a single replication deficient adenoviral vector. This consists of the CMV immediate early promotor driving expression of NR, with an internal ribosome entry site (IRES) and the gene for murine GM-CSF (mGM-CSF). To examine if similar enhancement of tumour cell killing could be produced in prostate cancer, the TRAMP model was chosen. Results illustrate that the combination of suicide gene therapy using NR and CB1954, with cytokine stimulation with mGM-CSF gives an improved response compared with either modality alone. The mechanism of this improved response is however likely to be non-immune based as it lacks a memory effect.

Indexed as

Genes, Transgenic, SuicideGenetic TherapyImmunotherapyAdenocarcinomaAdenoviridaeAnimalsAntineoplastic AgentsAziridinesBiotransformationCombined Modality TherapyDefective VirusesEscherichia coli ProteinsGenes, SyntheticGenetic VectorsGranulocyte-Macrophage Colony-Stimulating FactorMaleAntineoplastic AgentsAziridinesEscherichia coli ProteinsGranulocyte-Macrophage Colony-Stimulating FactorNfsA protein, E coliNitroreductasesProdrugsRecombinant Proteinstretazicar

Identifiers

PMID17726452
OpenAlexW2053553162

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.