Evidence map›Paper›PMID 39609428›Full record

ArticleNature communications2024

Transcription factors ASCL1 and OLIG2 drive glioblastoma initiation and co-regulate tumor cell types and migration.

Bianca L Myers, Kathryn J Brayer, Luis E Paez-Beltran, Estrella Villicana, Matthew S Keith, Hideaki Suzuki, Jessie Newville, Rebekka H Anderson, Yunee Lo, Conner M Mertz and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Rat Glioma 101.8 Tissue Strain: Molecular and Morphological Features.International journal of molecular sciences · 2025
    Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Genes · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Bianca L MyersDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0000-0001-8149-0643
Kathryn J BrayerUniversity of New Mexico Comprehensive Cancer Center, Albuquerque, NM, USA.
Luis E Paez-BeltranDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0009-0000-2223-5714
Estrella VillicanaDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0009-0008-6079-2827
Matthew S KeithDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Hideaki SuzukiDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Jessie NewvilleDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0000-0002-8590-7968
Rebekka H AndersonDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0000-0002-1080-936X
Yunee LoDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0009-0002-5002-4070
Conner M MertzDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.ORCID 0000-0001-8710-212X
Rahul K KolliparaMcDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Mark D BorromeoDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Q Richard LuDepartment of Pediatrics, Brain Tumor Center, EHCB, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID 0000-0001-6846-9014
Robert M BachooDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Jane E JohnsonDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-8605-2746
Tou Yia VueDepartment of Neurosciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA. TVue@salud.unm.edu.ORCID 0000-0002-5903-9968

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
University of New Mexico (UNM) Center for Brain Recovery and RepairP20GM109089 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI SHUTTLEWORTH, CLAUDE W · 2015 to 2024
$22.7M
Alcohol Research Training in NeurosciencesT32AA014127 · NIAAA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Jonathan L Brigman · 2003 to 2026
$3.3M
Transcriptional control of OPC fate specification and homing to gray matter and white matter in the CNSR01NS121660 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Tou Yia Vue · 2022 to 2026
$1.8M
Underlying Molecular Mechanisms of Gliogenesis and Gliomagenesis in the Central Nervous SystemK22NS092767 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI VUE, TOU YIA · 2015 to 2019
$886k
Role of Ascl1 in gliomaF32CA168330 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI VUE, TOU YIA · 2012 to 2014
$156k
Cancer Prevention and Research Institute of Texas (Cancer Prevention Research Institute of Texas) RP130464NCI NIH HHS F32 CA168330NCI NIH HHS P30 CA046934NCI NIH HHS P30 CA118100NIAAA NIH HHS T32 AA014127NIGMS NIH HHS P20 GM109089NINDS NIH HHS K22 NS092767NINDS NIH HHS R01 NS121660U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA046934U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA118100U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) P20GM109089U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) K22NS0967U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS121660
6 · The paper itself

Abstract

Glioblastomas (GBMs) are highly aggressive, infiltrative, and heterogeneous brain tumors driven by complex genetic alterations. The basic-helix-loop-helix (bHLH) transcription factors ASCL1 and OLIG2 are dynamically co-expressed in GBMs; however, their combinatorial roles in regulating the plasticity and heterogeneity of GBM cells are unclear. Here, we show that induction of somatic mutations in subventricular zone (SVZ) progenitor cells leads to the dysregulation of ASCL1 and OLIG2, which then function redundantly and are required for brain tumor formation in a mouse model of GBM. Subsequently, the binding of ASCL1 and OLIG2 to each other's loci and to downstream target genes then determines the cell types and degree of migration of tumor cells. Single-cell RNA sequencing (scRNA-seq) reveals that a high level of ASCL1 is key in specifying highly migratory neural stem cell (NSC)/astrocyte-like tumor cell types, which are marked by upregulation of ribosomal protein, oxidative phosphorylation, cancer metastasis, and therapeutic resistance genes.

Indexed as

Basic Helix-Loop-Helix ProteinsBrain NeoplasmsCell MovementGlioblastomaNeural Stem CellsOligodendrocyte Transcription Factor 2AnimalsAstrocytesCell Line, TumorGene Expression Regulation, NeoplasticHumansLateral VentriclesMiceMutationASCL1 protein, humanAscl1 protein, mouseBasic Helix-Loop-Helix ProteinsOLIG2 protein, humanOlig2 protein, mouseOligodendrocyte Transcription Factor 2

Identifiers

PMID39609428
PMCPMC11605073

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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.