Evidence map›Paper›PMID 42404419›Full record

ArticleBasic and clinical neuroscience2025

Vismodegib Improved Therapy of Medulloblastoma by Targeting Sonic Hedgehog Signaling Pathway on DAOY Medulloblastoma Cell Line.

Masume Behruzi, Mehrdad Ghorbanlou, Ronak Shabani, Auob Rustamzadeh, Enam Alhagh Gorgich, Elham Seidkhani, Farnoosh Usefi, Mehdi Mehdizadeh, Fatemeh Moradi

Abstract read
In one paragraph

Article in Basic and clinical neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

9 authors.

Masume BehruziDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0009-0004-3554-2755
Mehrdad GhorbanlouDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-5436-0074
Ronak ShabaniDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0003-3075-6071
Auob RustamzadehCellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran.ORCID https://orcid.org/0000-0002-8246-5631
Enam Alhagh GorgichDepartment of Anatomy, School of Medicine, Iranshahr University of Medical Sciences, Iranshahr, Iran.ORCID https://orcid.org/0000-0001-6817-8532
Elham SeidkhaniDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-2190-8910
Farnoosh UsefiDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0009-0009-6710-0974
Mehdi MehdizadehDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0002-2673-2715
Fatemeh MoradiDepartment of Anatomical Sciences, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0001-9231-280X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Targeting smoothened (SMO) has been a remarkable strategy for treating sonic hedgehog (Shh)-dependent cancers, especially medulloblastoma. GDC-0449, also known as vismodegib, is a potent SMO inhibitor with mild toxicity and high affinity. Thus, this study aimed to investigate the anti-medulloblastoma efficacy of vismodegib in the DAOY medulloblastoma cell line. Methods: Human DAOY medulloblastoma cells were cultured in Dulbecco's Modified Eagle's Medium (DMEM). 50, 80, 100, and 150 μM doses of vismodegib were used to treat cells. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), scratch, and trypan blue assays, as well as real-time polymerase chain reaction (RT-PCR) and immunofluorescence studies, were performed 24 and 48 h post-treatment. Results: The MTT and trypan blue assays showed a significant difference in viability between the control and treatment groups. The results of the scratch assay showed that in the control group, the cells were able to repair the lesion, while the scratch disintegrated at higher doses of vismodegib. The expression of Conclusion: The results of the current study confirm that vismodegib is a potent inhibitor of the Shh pathway and may be used in combination with new therapeutic methods to treat medulloblastoma.

Indexed as

Drug therapyMedulloblastomaNeoplasmToxicityVismodegib

Identifiers

PMID42404419
PMCPMC13332367

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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.