Evidence map›Paper›PMID 29158308›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2018

Glioblastoma multiforme-derived extracellular vesicles drive normal astrocytes towards a tumour-enhancing phenotype.

Soliman Oushy, Justin E Hellwinkel, Mary Wang, Ger J Nguyen, Dicle Gunaydin, Tessa A Harland, Thomas J Anchordoquy, Michael W Graner

Abstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
–field-weighted citation impact
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

74 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Review
  7. Article
  8. Review
  9. Reactive Astrocytes in Glioma: Emerging Opportunities and Challenges.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review

14 more citing papers are in PubMed but not listed here.

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

8 authors.

Soliman OushyUniversity of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID http://orcid.org/0000-0001-6343-6950
Justin E HellwinkelUniversity of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.
Mary WangDepartment of Neurosurgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045, USA.
Ger J NguyenDepartment of Neurosurgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045, USA.
Dicle GunaydinDepartment of Neurosurgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045, USA.
Tessa A HarlandUniversity of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO 80045, USA.
Thomas J AnchordoquySkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045, USA.
Michael W GranerDepartment of Neurosurgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO 80045, USA michael.graner@ucdenver.edu.ORCID http://orcid.org/0000-0002-3097-0257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is a devastating tumour with abysmal prognoses. We desperately need novel approaches to understand GBM biology and therapeutic vulnerabilities. Extracellular vesicles (EVs) are membrane-enclosed nanospheres released locally and systemically by all cells, including tumours, with tremendous potential for intercellular communication. Tumour EVs manipulate their local environments as well as distal targets; EVs may be a mechanism for tumourigenesis in the recurrent GBM setting. We hypothesized that GBM EVs drive molecular changes in normal human astrocytes (NHAs), yielding phenotypically tumour-promoting, or even tumourigenic, entities. We incubated NHAs with GBM EVs and examined the astrocytes for changes in cell migration, cytokine release and tumour cell growth promotion via the conditioned media. We measured alterations in intracellular signalling and transformation capacity (astrocyte growth in soft agar). GBM EV-treated NHAs displayed increased migratory capacity, along with enhanced cytokine production which promoted tumour cell growth. GBM EV-treated NHAs developed tumour-like signalling patterns and exhibited colony formation in soft agar, reminiscent of tumour cells themselves. GBM EVs modify the local environment to benefit the tumour itself, co-opting neighbouring astrocytes to promote tumour growth, and perhaps even driving astrocytes to a tumourigenic phenotype. Such biological activities could have profound impacts in the recurrent GBM setting.This article is part of the discussion meeting issue 'Extracellular vesicles and the tumour microenvironment'.

Indexed as

Cell ProliferationTumor MicroenvironmentAstrocytesCell Line, TumorCell MovementCytokinesExtracellular VesiclesGlioblastomaHumansPhenotypeCytokinesastrocytesexosomesextracellular vesiclesglioblastoma multiformemicroenvironmentsignalling

Identifiers

PMID29158308
PMCPMC5717433

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.