Evidence map›Paper›PMID 28084317›Full record

ArticleCancer gene therapy2017

Therapeutic vaccination based on side population cells transduced by the granulocyte-macrophage colony-stimulating factor gene elicits potent antitumor immunity.

C Sakamoto, H Kohara, H Inoue, M Narusawa, Y Ogawa, L Hirose-Yotsuya, S Miyamoto, Y Matsumura, K Yamada, A Takahashi and 1 more

Abstract read
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In one paragraph

Article in Cancer gene therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
  5. Novel targeted therapies in chronic myeloid leukemia.Pharmaceutical science advances · 2024
    Review
  6. Targeting neutrophils: Mechanism and advances in cancer therapy.Clinical and translational medicine · 2024
    Review
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  8. Review
  9. Article
  10. Review
  11. Article
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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

11 authors at 3 institutions in 1 country.

C SakamotoDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
H KoharaProject Division of ALA Advanced Medical Research, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
H InoueDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
M NarusawaDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Y OgawaProject Division of ALA Advanced Medical Research, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
L Hirose-YotsuyaProject Division of ALA Advanced Medical Research, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
S MiyamotoProject Division of ALA Advanced Medical Research, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Y MatsumuraDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
K YamadaDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
A TakahashiDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
K TaniDepartment of Molecular Genetics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Kyushu University · JPThe University of Tokyo · JPKyushu University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among cancer immunotherapies, granulocyte-macrophage colony-stimulating factor (GM-CSF) gene-transduced tumor cell vaccine (GVAX) therapies appear promising and have been shown to be safe and effective in multiple clinical trials. However, the antitumor efficacies of GVAX therapy alone are in some cases limited. Here we showed that GVAX therapy targeting cancer stem cells (CSCs) substantially suppressed tumor development in syngeneic immunocompetent mice recapitulating normal immune systems. CSCs were isolated as side population (SP) cells from 4T1 murine breast carcinoma cell line and transduced with GM-CSF gene delivered by non-transmissible Sendai virus (4T1-SP/GM). Impaired tumorigenicity of subcutaneously injected 4T1-SP/GM depended on CD8

Indexed as

Granulocyte-Macrophage Colony-Stimulating FactorImmunity, CellularMammary Neoplasms, ExperimentalAnimalsCD8-Positive T-LymphocytesCell Line, TumorFemaleMiceMice, Inbred BALB CSendai virusTh1 CellsTransduction, GeneticVaccinationGranulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID28084317
OpenAlexW2573143274

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.