Evidence map›Paper›PMID 10550313›Full record

ArticleThe American journal of pathology1999

Autocrine growth regulation by granulocyte colony-stimulating factor and granulocyte macrophage colony-stimulating factor in human gliomas with tumor progression.

M M Mueller, C C Herold-Mende, D Riede, M Lange, H H Steiner, N E Fusenig

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

45 citing papers in PubMed, 125 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Gene Expression ofInternational journal of molecular sciences · 2024
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  5. Review
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  7. Article
  8. Frequent Subgraph Mining of Functional Interaction Patterns Across Multiple Cancers.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2021
    Article
  9. Article
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Modeling the Hematopoietic Landscape.Frontiers in cell and developmental biology · 2019
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review
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 4 institutions in 2 countries.

M M MuellerDivision of Carcinogenesis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
C C Herold-Mende
D Riede
M Lange
H H Steiner
N E Fusenig
University Hospital Heidelberg · DEHeidelberg University · USHeidelberg University · DENephrologisches Zentrum Villingen-Schwenningen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Granulocyte colony-stimulating factor (G-CSF) and granulocyte macrophage colony-stimulating factor (GM-CSF) and/or their receptors are increasingly detected in solid human tumors, although little is known about their function in tumor growth and invasion. We analyzed RNA and protein expression of both factors and their receptors in 22 human gliomas (WHO grade II, III, and IV) and derived cell cultures. G-CSF, GM-CSF, and/or their receptors were expressed in all tumors and derived cell cultures, but coexpression of both factors and receptors was almost exclusively found in grade IV glioblastomas and thus correlated with advanced tumor stage. The functional significance of G-CSF and GM-CSF as regulators for glioma cells was demonstrated by 1) stimulation of proliferation and migration in tumor cells expressing one or both receptors by the corresponding factor; 2) inhibition of growth and migration of glioma cells expressing G-CSF, GM-CSF, and their receptors by neutralizing antibodies to both factors. These results indicate a significant role for both factors in the autocrine regulation of growth and migration in late-stage malignant gliomas and suggest a shift from paracrine to autocrine regulation with tumor progression. The implication of G-CSF and GM-CSF in glioblastoma growth regulation could make these factors further prognostic indicators and raises questions concerning their use in cancer therapy.

Indexed as

Autocrine CommunicationCell DifferentiationCell DivisionCentral Nervous System NeoplasmsGliomaGranulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorHumansReceptors, Granulocyte Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating FactorTumor Cells, CulturedGranulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorReceptors, Granulocyte Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID10550313
PMCPMC1866994
OpenAlexW2067873282

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.