Evidence map›Paper›PMID 38811170›Full record

ReviewGenes & development2024

Glioblastoma microenvironment-from biology to therapy.

Renee D Read, Zoe M Tapp, Prajwal Rajappa, Dolores Hambardzumyan

Abstract readReview
In one paragraph

Review in Genes & development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
–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

52 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

4 authors.

Renee D ReadDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia 30322, USA; dolores.hambardzumyan@mssm.edu renee.read@emory.edu prajwal.rajappa@nationwidechildrens.org.ORCID 0000-0002-5594-6958
Zoe M TappThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio 43205, USA.
Prajwal RajappaThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, Ohio 43205, USA; dolores.hambardzumyan@mssm.edu renee.read@emory.edu prajwal.rajappa@nationwidechildrens.org.
Dolores HambardzumyanDepartment of Oncological Sciences, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA; dolores.hambardzumyan@mssm.edu renee.read@emory.edu prajwal.rajappa@nationwidechildrens.org.ORCID 0000-0003-1975-4665

Funding

Tumor-Associated Macrophages in Vasogenic Cerebral Edema in Brain TumorsR01NS100864 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Dolores Hambardzumyan · 2017 to 2026
$5.4M
Verteporfin as a YAP/TAZ inhibitor for treatment of glioblastomaR01NS126348 · NINDS · EMORY UNIVERSITY · PI Renee D Read · 2023 to 2026
$2.3M
Mapping Immune Contexture and Crosstalk with Tumor Cells At GBM MarginR01NS134159 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAMBARDZUMYAN, DOLORES, ZOU, HONGYAN JENNY · 2023 to 2025
$2.0M
Bone marrow-derived myeloid cell dysregulation in malignant progression of gliomaR01NS127984 · NINDS · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Prajwal Rajappa · 2023 to 2026
$1.9M
Mechanisms of RIOK2 function in glioblastomaR01NS100967 · NINDS · EMORY UNIVERSITY · PI READ, RENEE D · 2017 to 2021
$1.7M
NINDS NIH HHS R01 NS100864NINDS NIH HHS R01 NS100967NINDS NIH HHS R01 NS126348NINDS NIH HHS R01 NS127984NINDS NIH HHS R01 NS134159
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive primary brain cancer. These tumors exhibit high intertumoral and intratumoral heterogeneity in neoplastic and nonneoplastic compartments, low lymphocyte infiltration, and high abundance of myeloid subsets that together create a highly protumorigenic immunosuppressive microenvironment. Moreover, heterogeneous GBM cells infiltrate adjacent brain tissue, remodeling the neural microenvironment to foster tumor electrochemical coupling with neurons and metabolic coupling with nonneoplastic astrocytes, thereby driving growth. Here, we review heterogeneity in the GBM microenvironment and its role in low-to-high-grade glioma transition, concluding with a discussion of the challenges of therapeutically targeting the tumor microenvironment and outlining future research opportunities.

Indexed as

Brain NeoplasmsGlioblastomaTumor MicroenvironmentAnimalsHumansglial cellsglioblastomaglioma stem celllymphoid cellsmyeloid cellsstem cell nichetumor microenvironment

Identifiers

PMID38811170
PMCPMC11216181

What OpenQuestion holds

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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.