Evidence map›Paper›PMID 31541075›Full record

ArticleCell death & disease2019

High impact of miRNA-4521 on FOXM1 expression in medulloblastoma.

Daniel Senfter, Mahzeiar Samadaei, Robert M Mader, Johannes Gojo, Andreas Peyrl, Georg Krupitza, Marcel Kool, Martin Sill, Christine Haberler, Gerda Ricken and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  8. Transcription Factors with Targeting Potential in Gliomas.International journal of molecular sciences · 2022
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  20. Circular RNAs and their participation in stemness of cancer.Medical oncology (Northwood, London, England) · 2020
    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 at 3 institutions in 2 countries.

Daniel SenfterDepartment of Pediatrics and Adolescent Medicine, Molecular Neuro-Oncology, Medical University of Vienna, Vienna, Austria.
Mahzeiar SamadaeiDepartment of Pediatrics and Adolescent Medicine, Molecular Neuro-Oncology, Medical University of Vienna, Vienna, Austria.
Robert M MaderComprehensive Cancer Center of the Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-3017-8240
Johannes GojoDepartment of Pediatrics and Adolescent Medicine, Molecular Neuro-Oncology, Medical University of Vienna, Vienna, Austria.
Andreas PeyrlDepartment of Pediatrics and Adolescent Medicine, Molecular Neuro-Oncology, Medical University of Vienna, Vienna, Austria.
Georg KrupitzaDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Marcel KoolHopp Children's Cancer Center at the NCT Heidelberg (KiTZ), Heidelberg, Germany.
Martin SillHopp Children's Cancer Center at the NCT Heidelberg (KiTZ), Heidelberg, Germany.
Christine HaberlerComprehensive Cancer Center of the Medical University of Vienna, Vienna, Austria.
Gerda RickenInstitute of Neurology, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-0388-7965
Thomas CzechComprehensive Cancer Center of the Medical University of Vienna, Vienna, Austria.
Irene SlavcDepartment of Pediatrics and Adolescent Medicine, Molecular Neuro-Oncology, Medical University of Vienna, Vienna, Austria.
Sibylle MadlenerDepartment of Pediatrics and Adolescent Medicine, Molecular Neuro-Oncology, Medical University of Vienna, Vienna, Austria. sibylle.madlener@meduniwien.ac.at.
Comprehensive Cancer Center Vienna · ATMedical University of Vienna · ATGerman Cancer Research Center · DE

Funding

Austrian Science Fund FWF I 3194
6 · The paper itself

Abstract

Medulloblastoma, an embryonal tumor of the cerebellum/fourth ventricle, is one of the most frequent malignant brain tumors in children. Although genetic variants are increasingly used in treatment stratification, survival of high-risk patients, characterized by leptomeningeal dissemination, TP53 mutation or MYC amplification, is still poor. FOXM1, a proliferation-specific oncogenic transcription factor, is deregulated in various solid tumors, including medulloblastoma, and triggers cellular proliferation, migration and genomic instability. In tissue samples obtained from medulloblastoma patients, the significant upregulation of FOXM1 was associated with a loss of its putative regulating microRNA, miR-4521. To understand the underlying mechanism, we investigated the effect of miR-4521 on the expression of the transcription factor FOXM1 in medulloblastoma cell lines. Transfection of this microRNA reduced proliferation and invasion of several medulloblastoma cell lines and induced programmed cell death through activation of caspase 3/7. Further, downstream targets of FOXM1 such as PLK1 and cyclin B1 were significantly reduced thus affecting the cell cycle progression in medulloblastoma cell lines. In conclusion, a restoration of miRNA-4521 may selectively suppress the pathophysiological effect of aberrant FOXM1 expression and serve as a targeted approach for medulloblastoma therapy.

Indexed as

3' Untranslated RegionsAdolescentBrain NeoplasmsCell Cycle CheckpointsCell Line, TumorCell ProliferationChildChild, PreschoolDown-RegulationFemaleForkhead Box Protein M1HumansInfantMaleMedulloblastomaMicroRNAs3' Untranslated RegionsForkhead Box Protein M1FOXM1 protein, humanMicroRNAsMIRN4521 microRNA, humanRNA, Messenger

Identifiers

PMID31541075
PMCPMC6754377
OpenAlexW2974278475

What OpenQuestion holds

Textmetadata
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.