Evidence map›Paper›PMID 41827847›Full record

ReviewCells2026

Neuro-Oncological Perspectives on Cancer Stem Cell Biology in Glioblastoma: Implications for Resection, Recurrence, Targeted Therapy, and Other CNS Tumors.

Karen Salmeron-Moreno, Karthik Papisetty, Chris Donghyun Kim, Thomas McCaffery, Rommi Kashlan, John Theodore, Jennifer Minseo Kim, Josephine Buclez, Hithardhi Duggireddy, Justin Maldonado and 3 more

Abstract readReview
In one paragraph

Review in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

13 authors.

Karen Salmeron-MorenoDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.ORCID 0000-0003-0555-0063
Karthik PapisettyDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.
Chris Donghyun KimDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.ORCID 0009-0004-1811-4118
Thomas McCafferyDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.
Rommi KashlanDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.
John TheodoreDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.
Jennifer Minseo KimDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.
Josephine BuclezDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.ORCID 0009-0001-5810-6364
Hithardhi DuggireddyDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.ORCID 0009-0001-7628-8851
Justin MaldonadoDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.
Hugo Guerrero-CázaresNeurosurgery Department, Mayo Clinic, Jacksonville, FL 32224, USA.ORCID 0000-0003-1307-719X
Gustavo PradillaDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.ORCID 0000-0002-3661-3269
Tomas Garzon-MuvdiDepartment of Neurological Surgery, Emory University, Atlanta, GA 30329, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells (CSCs) are increasingly recognized as central drivers of tumorigenesis, therapeutic resistance, and recurrence across diverse malignancies. This review synthesizes our current understanding of CSC biology across CNS tumors, with a focus on glioblastoma, where stem-like cells are sustained by specialized and overlapping tumor microenvironmental niches. Perivascular, hypoxic, invasive, immunosuppressive, and extracellular matrix-associated niches cooperatively enforce stemness, metabolic adaptability, immune evasion, and phenotypic plasticity, enabling CSC persistence despite maximal surgical resection and standard-of-care therapy. Notably, CSCs extend beyond radiographically defined tumor margins and populate peritumoral regions, providing a biological basis for near-universal recurrence. Advances in multiparametric imaging, stem cell-based ex vivo and in vivo models, and single-cell and spatial profiling have refined insight into CSC heterogeneity, niche dependence, and treatment resistance. Together, these findings reframe therapeutic strategies, highlighting the need for function-preserving maximal resection and multimodal therapies that target both CSC-intrinsic pathways and their supportive microenvironments.

Indexed as

Brain NeoplasmsCentral Nervous System NeoplasmsGlioblastomaMolecular Targeted TherapyNeoplasm Recurrence, LocalNeoplastic Stem CellsAnimalsHumansStem Cell NicheTumor Microenvironmentcancer stem cellsglioblastomanichestem-like cellstumor microenvironment

Identifiers

PMID41827847
PMCPMC12984708

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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.