Evidence map›Paper›PMID 30573757›Full record

ArticleScientific reports2018

Intratumoral heterogeneity of endogenous tumor cell invasive behavior in human glioblastoma.

Jonathon J Parker, Peter Canoll, Lee Niswander, B K Kleinschmidt-DeMasters, Kara Foshay, Allen Waziri

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Cell death in glioblastoma and the central nervous system.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Making In Vitro Tumor Models Whole Again.Advanced healthcare materials · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
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.

Jonathon J ParkerStanford University School of Medicine, Department of Neurosurgery, Stanford, CA, USA.
Peter CanollColumbia University College of Physicians and Surgeons, Department of Pathology and Cell Biology, New York, NY, USA.
Lee NiswanderUniversity of Colorado, Department of Molecular, Cellular & Developmental Biology, Boulder, CO, USA.
B K Kleinschmidt-DeMastersUniversity of Colorado School of Medicine, Department of Pathology, Anschutz Medical Campus, Aurora, CO, USA.
Kara FoshayInova Neuroscience and Spine Institute, Inova Health Systems, Falls Church, VA, USA. kara.foshay@inova.org.
Allen WaziriInova Neuroscience and Spine Institute, Inova Health Systems, Falls Church, VA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intratumoral genetic heterogeneity is a widely accepted characteristic of human cancer, including the most common primary malignant brain tumor, glioblastoma. However, the variability in biological behaviors amongst cells within individual tumors is not well described. Invasion into unaffected brain parenchyma is one such behavior, and a leading mechanism of tumor recurrence unaddressed by the current therapeutic armamentarium. Further, providing insight into variability of tumor cell migration within individual tumors may inform discovery of novel anti-invasive therapeutics. In this study, ex vivo organotypic slice cultures from EGFR-wild type and EGFR-amplified patient tumors were treated with the EGFR inhibitor gefitinib to evaluate potential sub-population restricted intratumoral drug-specific responses. High-resolution time-lapse microscopy and quantitative path tracking demonstrated migration of individual cells are punctuated by intermittent bursts of movement. Elevation of population aggregate mean speeds were driven by subpopulations of cells exhibiting frequent high-amplitude bursts, enriched within EGFR-amplified tumors. Treatment with gefitinib specifically targeted high-burst cell subpopulations only in EGFR-amplified tumors, decreasing bursting frequency and amplitude. We provide evidence of intratumoral subpopulations of cells with enhanced migratory behavior in human glioblastoma, selectively targeted via EGFR inhibition. These data justify use of direct human tumor slice cultures to investigate patient-specific therapies designed to limit tumor invasion.

Indexed as

Brain NeoplasmsCell MovementCell ProliferationDrug Screening Assays, AntitumorGefitinibGlioblastomaHumansNeoplasm InvasivenessPrimary Cell CultureTissue Culture TechniquesTumor Cells, CulturedGefitinib

Identifiers

PMID30573757
PMCPMC6301947

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Registered trials

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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.