Evidence map›Paper›PMID 17627292›Full record

ArticleCancer gene therapy2007

IL-12 gene-modified bone marrow cell therapy suppresses the development of experimental metastatic prostate cancer.

H Wang, G Yang, T L Timme, T Fujita, K Naruishi, A Frolov, M K Brenner, D Kadmon, T C Thompson

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

H WangScott Department of Urology, Baylor College of Medicine, Houston, TX 77030, USA.
G Yang
T L Timme
T Fujita
K Naruishi
A Frolov
M K Brenner
D Kadmon
T C Thompson
Baylor College of Medicine · US

Funding

PHS HHS P50-58204
6 · The paper itself

Abstract

To investigate the immunomodulatory effects of interleukin-12 (IL-12) for treatment of metastatic prostate cancer, we administered adult bone marrow cells (BMC) that were genetically modified by retroviral vector-mediated IL-12 gene transduction in an experimental mouse model of prostate cancer metastasis. This therapy produced significant anti-metastatic effects in bone and lung and prolonged animal survival. Flow cytometric analysis indicated donor BMC could effectively home to bone and lung after treatment. Intensive infiltration of CD4 and CD8T cells in lung metastases and increased systemic natural killer and cytotoxic T lymphocyte activities indicated induction of a significant anti-metastatic immune response after treatment with IL-12 transduced BMC. Our results demonstrate the therapeutic potential of gene-modified BMC gene therapy.

Indexed as

Disease Models, AnimalAnimalsBone Marrow CellsBone NeoplasmsGene ExpressionGenetic VectorsGreen Fluorescent ProteinsInterleukin-12Killer Cells, NaturalLung NeoplasmsMaleMiceProstatic NeoplasmsRetroviridaeSurvival RateT-Lymphocytes, Cytotoxicenhanced green fluorescent proteinGreen Fluorescent ProteinsInterleukin-12

Identifiers

PMID17627292
OpenAlexW2006376071

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.