Evidence map›Paper›PMID 42222374›Full record

ReviewFrontiers in oncology2026

Modeling gliomas with organoids: reconstructing the human neural microenvironment for translational neuro-oncology.

Mohamed Ishan, Jorge Luis Jimenez-Macias, Renee D Read

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Mohamed IshanDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, United States.
Jorge Luis Jimenez-MaciasDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, United States.
Renee D ReadDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gliomas represent some of the most lethal and biologically complex tumors of the central nervous system, with poor outcomes across both adult and pediatric populations. Beyond tumor-intrinsic genetic alterations, glioma progression is increasingly recognized to be driven by dynamic interactions with the neural microenvironment, particularly through direct tumor-neuron communication. Studies of adult and pediatric gliomas, including glioblastoma (GBM) and diffuse midline glioma (DMG), using single-cell profiling and multi-omics technologies have revealed extensive tumor intrinsic and extrinsic heterogeneity, with phenotypically and genetically plastic tumor cells actively engaged with neurons, glia, vasculature, and immune compartments that collectively reshape the neural microenvironment to promote tumor growth, invasion, and therapy resistance. Conventional two-dimensional

Indexed as

brain organoidscancer therapyglioblastomagliomaglioma organoidstumor invasiontumor microenvironmenttumor synapse

Identifiers

PMID42222374
PMCPMC13218870

What OpenQuestion holds

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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.