Evidence map›Paper›PMID 32253265›Full record

ArticleCancer discovery2020

Tumor Microenvironment Is Critical for the Maintenance of Cellular States Found in Primary Glioblastomas.

Allison R Pine, Stefano M Cirigliano, James G Nicholson, Yang Hu, Amanda Linkous, Ken Miyaguchi, Lincoln Edwards, Richa Singhania, Theodore H Schwartz, Rohan Ramakrishna and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed, 1 pooled it
14.5field-weighted citation impact, top 1% 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

104 citing papers in PubMed, 1 synthesis or guideline pooled it, 170 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 2 countries.

Allison R Pine *Caryl and Israel Englander Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, New York.
Stefano M Cirigliano *Department of Neurology, Weill Cornell Medicine, New York, New York.
James G NicholsonDepartment of Neurology, Weill Cornell Medicine, New York, New York.ORCID https://orcid.org/0000-0002-4585-6924
Yang HuCaryl and Israel Englander Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, New York.ORCID https://orcid.org/0000-0002-6348-874X
Amanda LinkousDepartment of Neurology, Weill Cornell Medicine, New York, New York.ORCID https://orcid.org/0000-0003-1663-6364
Ken MiyaguchiDepartment of Neurology, Weill Cornell Medicine, New York, New York.
Lincoln EdwardsBrain and Mind Research Institute, Weill Cornell Medicine, New York, New York.
Richa SinghaniaDepartment of Neurology, Weill Cornell Medicine, New York, New York.
Theodore H SchwartzDepartment of Neurological Surgery, Weill Cornell Medicine, New York, New York.ORCID https://orcid.org/0000-0003-4464-7394
Rohan RamakrishnaDepartment of Neurological Surgery, Weill Cornell Medicine, New York, New York.
David J PisapiaDepartment of Pathology, Weill Cornell Medicine, New York, New York.
Matija SnuderlDepartment of Pathology, NYU Langone Medical Center, New York, New York.
Olivier ElementoCaryl and Israel Englander Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, New York. haf9016@med.cornell.edu ole2001@med.cornell.edu.
Howard A FineDepartment of Neurology, Weill Cornell Medicine, New York, New York. haf9016@med.cornell.edu ole2001@med.cornell.edu.
Cornell University · USNYU Langone Health · US

Funding

Human Brain Cancer, Rather than Brain Cancer Cells, on a PlateDP1CA228040 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI FINE, HOWARD A. · 2017 to 2021
$5.9M
Tri-Institutional Training Program in Computational Biology & MedicineT32GM083937 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHRISTINI, DAVID J. · 2009 to 2018
$3.1M
NCI NIH HHS DP1 CA228040NIGMS NIH HHS T32 GM083937
6 · The paper itself

Abstract

Glioblastoma (GBM), an incurable tumor, remains difficult to model and more importantly to treat due to its genetic/epigenetic heterogeneity and plasticity across cellular states. The ability of current tumor models to recapitulate the cellular states found in primary tumors remains unexplored. To address this issue, we compared single-cell RNA sequencing of tumor cells from 5 patients across four patient-specific glioblastoma stem cell (GSC)-derived model types, including glioma spheres, tumor organoids, glioblastoma cerebral organoids (GLICO), and patient-derived xenografts. We find that GSCs within the GLICO model are enriched for a neural progenitor-like cell subpopulation and recapitulate the cellular states and their plasticity found in the corresponding primary parental tumors. These data demonstrate how the contribution of a neuroanatomically accurate human microenvironment is critical and sufficient for recapitulating the cellular states found in human primary GBMs, a principle that may likely apply to other tumor models. SIGNIFICANCE: It has been unclear how well different patient-derived GBM models are able to recreate the full heterogeneity of primary tumors. Here, we provide a complete transcriptomic characterization of the major model types. We show that the microenvironment is crucial for recapitulating GSC cellular states, highlighting the importance of tumor-host cell interactions.

Indexed as

GlioblastomaHumansTumor Microenvironment

Identifiers

PMID32253265
PMCPMC10256258
OpenAlexW3014253386

What OpenQuestion holds

Textmetadata
LicenceTDM
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.