Evidence map›Paper›PMID 39043693›Full record

ArticleNature communications2024

Multiomic profiling of medulloblastoma reveals subtype-specific targetable alterations at the proteome and N-glycan level.

Shweta Godbole, Hannah Voß, Antonia Gocke, Simon Schlumbohm, Yannis Schumann, Bojia Peng, Martin Mynarek, Stefan Rutkowski, Matthias Dottermusch, Mario M Dorostkar and 17 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

27 authors.

Shweta Godbole *Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5162-5233
Hannah Voß *Section of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Antonia GockeCenter for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0009-0007-5828-6637
Simon SchlumbohmChair for High Performance Computing, Helmut Schmidt University, Hamburg, Germany.
Yannis SchumannChair for High Performance Computing, Helmut Schmidt University, Hamburg, Germany.ORCID 0000-0002-2379-200X
Bojia PengSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Martin MynarekDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-3302-2719
Stefan RutkowskiDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Matthias DottermuschCenter for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-9769-7080
Mario M DorostkarCenter for Neuropathology, Ludwig-Maximilians-University, Munich, Germany.
Andrey KorshunovDepartment of Neuropathology, University Hospital Heidelberg, Heidelberg, Germany.
Thomas MairSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stefan M PfisterHopp Children's Cancer Center at the NCT Heidelberg (KiTZ), Heidelberg, Germany.ORCID 0000-0002-5447-5322
Marcel KwiatkowskiInstitute of Biochemistry, University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-5804-6031
Madlen HotzeInstitute of Biochemistry, University of Innsbruck, Innsbruck, Austria.
Philipp NeumannChair for High Performance Computing, Helmut Schmidt University, Hamburg, Germany.ORCID 0000-0001-8604-8846
Christian HartmannDepartment of Neuropathology, Hannover Medical School (MHH), Hannover, Germany.
Joachim WeisInstitute of Neuropathology, RWTH Aachen University Hospital, Aachen, Germany.ORCID 0000-0003-3280-6773
Friederike Liesche-StarneckerPathology, Medical Faculty, University of Augsburg, Augsburg, Germany.
Yudong GuanSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Manuela MoritzSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Bente SiebelsSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Nina StruveMildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Hartmut SchlüterSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Ulrich SchüllerInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8731-1121
Christoph KrispSection of Mass Spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-4689-1967
Julia E NeumannCenter for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany. ju.neumann@uke.de.ORCID 0000-0002-1162-8771

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 416054672
6 · The paper itself

Abstract

Medulloblastomas (MBs) are malignant pediatric brain tumors that are molecularly and clinically heterogenous. The application of omics technologies-mainly studying nucleic acids-has significantly improved MB classification and stratification, but treatment options are still unsatisfactory. The proteome and their N-glycans hold the potential to discover clinically relevant phenotypes and targetable pathways. We compile a harmonized proteome dataset of 167 MBs and integrate findings with DNA methylome, transcriptome and N-glycome data. We show six proteome MB subtypes, that can be assigned to two main molecular programs: transcription/translation (pSHHt, pWNT and pG3myc), and synapses/immunological processes (pSHHs, pG3 and pG4). Multiomic analysis reveals different conservation levels of proteome features across MB subtypes at the DNA methylome level. Aggressive pGroup3myc MBs and favorable pWNT MBs are most similar in cluster hierarchies concerning overall proteome patterns but show different protein abundances of the vincristine resistance-associated multiprotein complex TriC/CCT and of N-glycan turnover-associated factors. The N-glycome reflects proteome subtypes and complex-bisecting N-glycans characterize pGroup3myc tumors. Our results shed light on targetable alterations in MB and set a foundation for potential immunotherapies targeting glycan structures.

Indexed as

MedulloblastomaPolysaccharidesProteomeCerebellar NeoplasmsChildChild, PreschoolDNA MethylationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleProteomicsTranscriptomePolysaccharidesProteome

Identifiers

PMID39043693
PMCPMC11266559

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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.