Evidence map›Paper›PMID 35906273›Full record

ArticleNPJ precision oncology2022

A patient-designed tissue-engineered model of the infiltrative glioblastoma microenvironment.

R C Cornelison, J X Yuan, K M Tate, A Petrosky, G F Beeghly, M Bloomfield, S C Schwager, A L Berr, C A Stine, D Cimini and 5 more

Open access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  7. Microfabricated Organ-Specific Models of Tumor Microenvironments.Annual review of biomedical engineering · 2025
    Review
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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

15 authors at 4 institutions in 1 country.

R C Cornelison *Department of Biomedical Engineering, University of Massachusetts Amherst, Amherst, MA, 01003, USA.ORCID http://orcid.org/0000-0002-0651-717X
J X Yuan *Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, 22904, USA.
K M TateDepartment of Biomedical Engineering & Mechanics, Virginia Tech, Blacksburg, VA, 24061, USA.
A PetroskyDepartment of Biomedical Engineering & Mechanics, Virginia Tech, Blacksburg, VA, 24061, USA.
G F BeeghlyDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, 22904, USA.ORCID http://orcid.org/0000-0002-4726-5896
M BloomfieldDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA, 24061, USA.ORCID http://orcid.org/0000-0002-1782-081X
S C SchwagerDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, 22904, USA.
A L BerrDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, 22904, USA.
C A StineDepartment of Biomedical Engineering & Mechanics, Virginia Tech, Blacksburg, VA, 24061, USA.ORCID http://orcid.org/0000-0002-7540-9316
D CiminiDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA, 24061, USA.ORCID http://orcid.org/0000-0002-4082-4894
F F BafakihUniversity of Virginia School of Medicine, Charlottesville, VA, 22903, USA.
J W MandellUniversity of Virginia School of Medicine, Charlottesville, VA, 22903, USA.
B W PurowUniversity of Virginia School of Medicine, Charlottesville, VA, 22903, USA.
B J HortonUniversity of Virginia School of Medicine, Charlottesville, VA, 22903, USA.
J M MunsonDepartment of Biomedical Engineering & Mechanics, Virginia Tech, Blacksburg, VA, 24061, USA. munsonj@vt.edu.ORCID http://orcid.org/0000-0002-9477-1505
University of Virginia · USBiomedical Research Institute · USVirginia Tech · USUniversity of Massachusetts Amherst · US

Funding

Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
Interstitial Fluid Flow Regulates Glioma Cell InvasionR37CA222563 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI MUNSON, JENNIFER M · 2018 to 2024
$4.0M
Combining modeling and experiments to study the evolution of cells with altered ploidyR01GM140042 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI CIMINI, DANIELA, SCHMELZ, EVA M. · 2021 to 2024
$1.4M
NCI NIH HHS R37 CA222563NCI NIH HHS T32 CA009109NIGMS NIH HHS R01 GM140042
6 · The paper itself

Abstract

Glioblastoma is an aggressive brain cancer characterized by diffuse infiltration. Infiltrated glioma cells persist in the brain post-resection where they interact with glial cells and experience interstitial fluid flow. We use patient-derived glioma stem cells and human glial cells (i.e., astrocytes and microglia) to create a four-component 3D model of this environment informed by resected patient tumors. We examine metrics for invasion, proliferation, and putative stemness in the context of glial cells, fluid forces, and chemotherapies. While the responses are heterogeneous across seven patient-derived lines, interstitial flow significantly increases glioma cell proliferation and stemness while glial cells affect invasion and stemness, potentially related to CCL2 expression and differential activation. In a screen of six drugs, we find in vitro expression of putative stemness marker CD71, but not viability at drug IC

Identifiers

PMID35906273
PMCPMC9338058
OpenAlexW4288514634

What OpenQuestion holds

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LicenceCC BY
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.