Evidence map›Paper›PMID 33175161›Full record

ArticleNeuro-oncology2021

An extracellular vesicle-related gene expression signature identifies high-risk patients in medulloblastoma.

Thomas K Albert, Marta Interlandi, Martin Sill, Monika Graf, Natalia Moreno, Kerstin Menck, Astrid Rohlmann, Viktoria Melcher, Sonja Korbanka, Gerd Meyer Zu Hörste and 12 more

Abstract read
In one paragraph

Article in Neuro-oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. CTC, ctDNA, and Exosome in Thyroid Cancers: A Review.International journal of molecular sciences · 2023
    Review
  7. Group-specific cellular metabolism in Medulloblastoma.Journal of translational medicine · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Thomas K AlbertDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Marta InterlandiDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Martin SillHopp-Children's Cancer Center at the NCT Heidelberg (KiTZ), Heidelberg, Germany.
Monika GrafDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Natalia MorenoDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Kerstin MenckDepartment of Medicine A, Hematology, Oncology, and Pneumology, University Hospital Münster (UKM), Münster, Germany.
Astrid RohlmannDepartment of Medicine A, Hematology, Oncology, and Pneumology, University Hospital Münster (UKM), Münster, Germany.
Viktoria MelcherDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Sonja KorbankaDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Gerd Meyer Zu HörsteDepartment of Neurology, UKM, Münster, Germany.
Tobias LautweinBiological and Medical Research Center, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Michael C FrühwaldSwabian Children's Cancer Center, Children's Hospital Augsburg, Augsburg, Germany.
Christian F KrebsCenter for Internal Medicine, III. Medical Clinic and Polyclinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Dörthe HoldhofDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Melanie SchoofDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Annalen BleckmannDepartment of Medicine A, Hematology, Oncology, and Pneumology, University Hospital Münster (UKM), Münster, Germany.
Markus MisslerDepartment of Anatomy and Molecular Neurobiology, WWU Münster, Münster, Germany.
Martin DugasInstitute of Medical Informatics, Westphalian-Wilhelms-University (WWU) Münster, Münster, Germany.
Ulrich SchüllerDepartment of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Natalie JägerHopp-Children's Cancer Center at the NCT Heidelberg (KiTZ), Heidelberg, Germany.
Stefan M PfisterHopp-Children's Cancer Center at the NCT Heidelberg (KiTZ), Heidelberg, Germany.
Kornelius KerlDepartment of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMedulloblastoma (MB) is a malignant brain tumor in childhood. It comprises 4 subgroups with different clinical behaviors. The aim of this study was to characterize the transcriptomic landscape of MB, both at the level of individual tumors as well as in large patient cohorts.

methodsWe used a combination of single-cell transcriptomics, cell culture models and biophysical methods such as nanoparticle tracking analysis and electron microscopy to investigate intercellular communication in the MB tumor niche.

resultsTumor cells of the sonic hedgehog (SHH)-MB subgroup show a differentiation blockade. These cells undergo extensive metabolic reprogramming. The gene expression profiles of individual tumor cells show a partial convergence with those of tumor-associated glial and immune cells. One possible cause is the transfer of extracellular vesicles (EVs) between cells in the tumor niche. We were able to detect EVs in co-culture models of MB tumor cells and oligodendrocytes. We also identified a gene expression signature, EVS, which shows overlap with the proteome profile of large oncosomes from prostate cancer cells. This signature is also present in MB patient samples. A high EVS expression is one common characteristic of tumors that occur in high-risk patients from different MB subgroups or subtypes.

conclusionsWith EVS, our study uncovered a novel gene expression signature that has a high prognostic significance across MB subgroups.

Indexed as

Cerebellar NeoplasmsExtracellular VesiclesMedulloblastomaHedgehog ProteinsHumansMaleTranscriptomeHedgehog Proteinsextracellular vesiclegene expression signaturemedulloblastomasingle-cell RNA sequencingtumor microenvironment

Identifiers

PMID33175161
PMCPMC8041350

What Socratic holds

Textmetadata
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 Socratic graph.