Evidence map›Paper›PMID 41972666›Full record

ReviewCells2026

Human Cytomegalovirus as a Therapeutic Target in Glioma Stem Cells.

Tarek Bou Dargham, Eugene J Vaios, Sean Lawler, Kristen Batich

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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Tarek Bou DarghamDepartment of Neurosurgery, Duke University, Durham, NC 27710, USA.
Eugene J VaiosThe Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0003-2122-6650
Sean LawlerDepartment of Pathology and Laboratory Medicine, Legorreta Cancer Center, Brown University, Providence, RI 02903, USA.
Kristen BatichDepartment of Neurosurgery, Duke University, Durham, NC 27710, USA.ORCID 0000-0002-8699-8769

Funding

Conquer Cancer Foundation of the American Society of Clinical Oncology (ASCO) Young Investigator AwardDuke Cancer Institute (DCI) Allin Family FellowshipDuke Cancer Institute (DCI) Pilot ProjectDuke Clinical and Translational Science Award NIH UL1TR002553Duke SPORE in Brain Cancer Career Enhancement Program (CEP)
6 · The paper itself

Abstract

Glioblastoma is the most aggressive tumor among gliomas, and recurrence remains inevitable despite aggressive therapies. Resistance to existing treatment modalities is attributed in part to the presence of glioma stem cells, which comprise a distinct cell subpopulation that sustains cell renewal and tumor evasion through multiple mechanisms. Therapeutic strategies using herpesviruses have been evaluated following the discovery of differential human cytomegalovirus (HCMV) expression in glioblastoma tumor cells. The absence of expression in normal brain tissue led to multiple clinical trials demonstrating the potential clinical utility of targeted HCMV via herpesvirus-based oncolytic therapeutic strategies. This review provides a comprehensive overview of existing studies evaluating the expression and biological significance of HCMV within glioma stem cells. Targeting HCMV in this cellular compartment may disrupt the continuous cellular support and resilience of glioblastoma stem cells, thereby enhancing the efficacy of current treatments.

Indexed as

Brain NeoplasmsCytomegalovirusGlioblastomaGliomaNeoplastic Stem CellsAnimalsHumansglioblastomagliomaglioma stem cellshuman cytomegalovirustargeted therapy

Identifiers

PMID41972666
PMCPMC13072111

What OpenQuestion holds

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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.