Evidence map›Paper›PMID 35398668›Full record

ArticleNeoplasia (New York, N.Y.)2022

Phenotypic and molecular states of IDH1 mutation-induced CD24-positive glioma stem-like cells.

Sara Haddock, Tyler J Alban, Şevin Turcan, Hana Husic, Eric Rosiek, Xiaoxiao Ma, Yuxiang Wang, Tejus Bale, Alexis Desrichard, Vladimir Makarov and 6 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Brain Tumor Stem Cells: New Perspectives.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  6. Mesenchymal Properties of Glioma Cell Lines.Bulletin of experimental biology and medicine · 2024
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
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

16 authors at 4 institutions in 3 countries.

Sara HaddockWeill Cornell School of Medicine, New York, NY 10021, USA; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Tyler J AlbanCenter for Immunotherapy and Precision Immuno-Oncology, Cleveland Clinic, Cleveland, OH 44022, USA.
Şevin TurcanNeurology Clinic and National Center for Tumor Diseases, Heidelberg University Hospital, Heidelberg, Germany.
Hana HusicCenter for Immunotherapy and Precision Immuno-Oncology, Cleveland Clinic, Cleveland, OH 44022, USA.
Eric RosiekDepartment of Molecular Cytology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Xiaoxiao MaCenter for Immunotherapy and Precision Immuno-Oncology, Cleveland Clinic, Cleveland, OH 44022, USA.
Yuxiang WangDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.
Tejus BaleDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Alexis DesrichardHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Vladimir MakarovCenter for Immunotherapy and Precision Immuno-Oncology, Cleveland Clinic, Cleveland, OH 44022, USA.
Sebastien MonetteLaboratory of Comparative Pathology, Memorial Sloan Kettering Cancer Center, The Rockefeller University, Weill Cornell Medicine, New York, NY 10065, USA.
Wei WuHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Rui GardnerFlow Cytometry Core, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Katia ManovaDepartment of Molecular Cytology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Adrienne BoireHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Timothy A ChanHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Center for Immunotherapy and Precision Immuno-Oncology, Cleveland Clinic, Cleveland, OH 44022, USA; Case Western School of Medicine, Cleveland, OH 44106, USA. Electronic address: chant2@ccf.org.
Memorial Sloan Kettering Cancer Center · USCleveland Clinic · USHeidelberg University · DEShanghai Medical College of Fudan University · CN

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
TOWARDS PRECISION IMMUNO-ONCOLOGY: UNRAVELING THE GENOMIC DETERMINANTS AND MECHANISMS UNDERLYING IMMUNOTHERAPY EFFICACY AND RESISTANCER35CA232097 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHAN, TIMOTHY AN-THY · 2018 to 2024
$7.0M
RESEARCH ONCOLOGY TRAINING GRANTT32CA059366 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI JACKSON, MARK W. · 1993 to 2025
$5.5M
Elucidating genetics of response to immune checkpoint blockade in lung cancerR01CA205426 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHAN, TIMOTHY AN-THY, RIZVI, NAIYER A · 2017 to 2021
$3.2M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA205426NCI NIH HHS R35 CA232097NCI NIH HHS T32 CA059366
6 · The paper itself

Abstract

Mutations in IDH1 and IDH2 drive the development of gliomas. These genetic alterations promote tumor cell renewal, disrupt differentiation states, and induce stem-like properties. Understanding how this phenotypic reprogramming occurs remains an area of high interest in glioma research. Previously, we showed that IDH mutation results in the development of a CD24-positive cell population in gliomas. Here, we demonstrate that this CD24-positive population possesses striking stem-like properties at the molecular and phenotypic levels. We found that CD24 expression is associated with stem-like features in IDH-mutant tumors, a patient-derived gliomasphere model, and a neural stem cell model of IDH1-mutant glioma. In orthotopic models, CD24-positive cells display enhanced tumor initiating potency compared to CD24-negative cells. Furthermore, CD24 knockdown results in changes in cell viability, proliferation rate, and gene expression that closely resemble a CD24-negative phenotype. Our data demonstrate that induction of a CD24-positive population is one mechanism by which IDH-mutant tumors acquire stem-like properties. These findings have significant implications for our understanding of the molecular underpinnings of IDH-mutant gliomas.

Indexed as

Brain NeoplasmsGliomaIsocitrate DehydrogenaseNeoplastic Stem CellsCD24 AntigenHumansMutationPhenotypeCD24 AntigenCD24 protein, humanIDH1 protein, humanIsocitrate Dehydrogenasecancer stem cellsCD24IDH1 mutationLow-grade gliomaNeural stem cellsOrthotopic mouse model

Identifiers

PMID35398668
PMCPMC9014446
OpenAlexW4223505646

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.