Evidence map›Paper›PMID 42122149›Full record

ReviewCancers2026

Targeting Glioblastoma Stem Cells: Therapeutic Strategies and Clinical Perspectives.

Harikrishna Reddy Rachamala, Sonia Devi Lourembam, Debabrata Mukhopadhyay, Ramcharan Singh Angom

Abstract readReview
In one paragraph

Review in Cancers, 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

4 authors.

Harikrishna Reddy RachamalaDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA.ORCID 0000-0003-0514-4428
Sonia Devi LourembamDepartment of Transplant Immunology and Immunogenetics, All India Institute of Medical Science, Delhi 110029, India.
Debabrata MukhopadhyayDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA.ORCID 0000-0003-1858-5054
Ramcharan Singh AngomDepartment of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA.ORCID 0000-0002-5894-1108

Funding

Florida Department of Health 91803004 (DM)Innovation in Aging (Mayo CCaTS) UL1TR002377National Heart Lung and Blood Institute HL 140411National Institute of Health (NIH) CA150190National Institute of Health (NIH) CA78383National Institute of Health (NIH) NS129671-1(DM)
6 · The paper itself

Abstract

With limited therapeutic progress despite aggressive multimodal treatment, glioblastoma (GBM) remains one of the deadliest primary brain tumors. Emerging evidence suggests that GSCs are key drivers of tumor initiation, intratumoral heterogeneity, therapeutic resistance, and recurrence. GSCs retain self-renewal capacity, multilineage differentiation potential, and remarkable plasticity, enabling them to adapt to diverse microenvironmental cues. These properties are upheld by dysregulated developmental and oncogenic signaling pathways, including Notch, Wnt/β-catenin, Hedgehog, PI3K/AKT/mTOR, and STAT3, as well as epigenetic and metabolic reprogramming. In addition, dedicated niches such as hypoxic and perivascular microenvironments critically support GSC maintenance and immune evasion. In this review, we summarize the current understanding of the molecular pathways governing GSC biology, examine their interactions with the tumor microenvironment, and discuss emerging therapeutic strategies targeting GSCs, including pathway inhibition, differentiation therapy, immunotherapy, and nanomedicine-based drug delivery. We highlight key challenges and future directions for translating GSC-targeted approaches into effective clinical interventions for GBM.

Indexed as

cancer stem cell nicheglioblastomaglioblastoma stem cellsprecision oncologytargeted therapytherapy resistancetumor microenvironment

Identifiers

PMID42122149
PMCPMC13162718

What OpenQuestion holds

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LicenceCC BY
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.