Evidence map›Paper›PMID 40980444›Full record

ArticleNeuro-oncology advances

Effect of focused ultrasound-induced mechanical ablation on stemness and dormancy properties of residual/peri-focally localized glioblastoma cells.

Dana Hellmold, Levi Johanning, Jacqueline Clüver, Jonna Holler, Nils Oliver Schröder, Frieda Bayler, Hajrullah Ahmeti, Carolin Kubelt-Kwamin, Sina Wieker, Ann-Kristin Helmers and 2 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. 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. Article
  2. 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

12 authors.

Dana HellmoldDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Levi JohanningDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Jacqueline ClüverDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Jonna HollerDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Nils Oliver SchröderDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Frieda BaylerDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Hajrullah AhmetiDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Carolin Kubelt-KwaminDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Sina WiekerDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Ann-Kristin HelmersDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Michael SynowitzDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.
Janka Held-FeindtDepartment of Neurosurgery, University Medical Center Schleswig-Holstein (UKSH), 24105 Kiel, Germany.ORCID https://orcid.org/0000-0002-1304-2694

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Focused ultrasound (FUS) is a new technology that enables the spatially and temporally precise delivery of ultrasound energy to various targets. In addition to its known applications in treating tumors, cavitation-based mechanical focused ultrasound (mFUS) is gaining importance. Due to the novelty of this technique, little is known about the effects of mFUS on peri-focally localized or surviving tumor cells. Glioblastomas (GBMs) are highly malignant intracranial tumors with a pronounced intra- and intertumoral heterogeneity, which, eg leads to their evasion of appropriate treatment regimens. Methods: The impact of mFUS was investigated in patient-derived GBM organoids (GBOs), glioma stem-like cells (GSCs), and differentiated GBM cells in an in vitro 3D hydrogel culture model. Particular attention was paid to investigating the stemness and dormancy properties of residual/peri-focally localized GBM cells, as these may be important for tumor progression. Results: In GBOs and different primary cells, increased expression of dormancy- and stemness-associated markers was found in a complex region- and marker-dependent manner mediated via PI3-kinase/Akt/GSK3β signaling, suggesting an effect of mFUS beyond the focal area. mFUS resulted in an increased ability of residual/peri-focal, formerly differentiated patient-derived GBM cells to form stem cell-typical spheres associated with increased expression of various dormancy and stemness markers. Residual/peri-focal patient-derived cells were characterized by a higher resistance to temozolomide, resulting in fewer dead cells compared to temozolomide treatment alone. Conclusion: The ablation of defined regions by mFUS appears to regulate the stemness and dormancy properties of the residual/peri-focally localized GBM cells in a region-specific manner.

Indexed as

dormancyglioblastomamechanical focused ultrasoundstemness

Identifiers

PMID40980444
PMCPMC12449158

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