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

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An extracellular vesicle-related gene expression signature identifies high-risk patients in medulloblastoma. / Albert, Thomas K; Interlandi, Marta; Sill, Martin; Graf, Monika; Moreno, Natalia; Menck, Kerstin; Rohlmann, Astrid; Melcher, Viktoria; Korbanka, Sonja; Meyer Zu Hörste, Gerd; Lautwein, Tobias; Frühwald, Michael C; Krebs, Christian F; Holdhof, Dörthe; Schoof, Melanie; Bleckmann, Annalen; Missler, Markus; Dugas, Martin; Schüller, Ulrich; Jäger, Natalie; Pfister, Stefan M; Kerl, Kornelius.

in: NEURO-ONCOLOGY, Jahrgang 23, Nr. 4, 12.04.2021, S. 586-598.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Albert, TK, Interlandi, M, Sill, M, Graf, M, Moreno, N, Menck, K, Rohlmann, A, Melcher, V, Korbanka, S, Meyer Zu Hörste, G, Lautwein, T, Frühwald, MC, Krebs, CF, Holdhof, D, Schoof, M, Bleckmann, A, Missler, M, Dugas, M, Schüller, U, Jäger, N, Pfister, SM & Kerl, K 2021, 'An extracellular vesicle-related gene expression signature identifies high-risk patients in medulloblastoma', NEURO-ONCOLOGY, Jg. 23, Nr. 4, S. 586-598. https://doi.org/10.1093/neuonc/noaa254

APA

Albert, T. K., Interlandi, M., Sill, M., Graf, M., Moreno, N., Menck, K., Rohlmann, A., Melcher, V., Korbanka, S., Meyer Zu Hörste, G., Lautwein, T., Frühwald, M. C., Krebs, C. F., Holdhof, D., Schoof, M., Bleckmann, A., Missler, M., Dugas, M., Schüller, U., ... Kerl, K. (2021). An extracellular vesicle-related gene expression signature identifies high-risk patients in medulloblastoma. NEURO-ONCOLOGY, 23(4), 586-598. https://doi.org/10.1093/neuonc/noaa254

Vancouver

Bibtex

@article{d5a4f15ac83848069cc42dfd39ecc139,
title = "An extracellular vesicle-related gene expression signature identifies high-risk patients in medulloblastoma",
abstract = "BACKGROUND: Medulloblastoma (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.METHODS: We 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.RESULTS: Tumor 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.CONCLUSIONS: With EVS, our study uncovered a novel gene expression signature that has a high prognostic significance across MB subgroups.",
author = "Albert, {Thomas K} and Marta Interlandi and Martin Sill and Monika Graf and Natalia Moreno and Kerstin Menck and Astrid Rohlmann and Viktoria Melcher and Sonja Korbanka and {Meyer Zu H{\"o}rste}, Gerd and Tobias Lautwein and Fr{\"u}hwald, {Michael C} and Krebs, {Christian F} and D{\"o}rthe Holdhof and Melanie Schoof and Annalen Bleckmann and Markus Missler and Martin Dugas and Ulrich Sch{\"u}ller and Natalie J{\"a}ger and Pfister, {Stefan M} and Kornelius Kerl",
note = "{\textcopyright} The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.",
year = "2021",
month = apr,
day = "12",
doi = "10.1093/neuonc/noaa254",
language = "English",
volume = "23",
pages = "586--598",
journal = "NEURO-ONCOLOGY",
issn = "1522-8517",
publisher = "Oxford University Press",
number = "4",

}

RIS

TY - JOUR

T1 - An extracellular vesicle-related gene expression signature identifies high-risk patients in medulloblastoma

AU - Albert, Thomas K

AU - Interlandi, Marta

AU - Sill, Martin

AU - Graf, Monika

AU - Moreno, Natalia

AU - Menck, Kerstin

AU - Rohlmann, Astrid

AU - Melcher, Viktoria

AU - Korbanka, Sonja

AU - Meyer Zu Hörste, Gerd

AU - Lautwein, Tobias

AU - Frühwald, Michael C

AU - Krebs, Christian F

AU - Holdhof, Dörthe

AU - Schoof, Melanie

AU - Bleckmann, Annalen

AU - Missler, Markus

AU - Dugas, Martin

AU - Schüller, Ulrich

AU - Jäger, Natalie

AU - Pfister, Stefan M

AU - Kerl, Kornelius

N1 - © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

PY - 2021/4/12

Y1 - 2021/4/12

N2 - BACKGROUND: Medulloblastoma (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.METHODS: We 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.RESULTS: Tumor 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.CONCLUSIONS: With EVS, our study uncovered a novel gene expression signature that has a high prognostic significance across MB subgroups.

AB - BACKGROUND: Medulloblastoma (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.METHODS: We 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.RESULTS: Tumor 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.CONCLUSIONS: With EVS, our study uncovered a novel gene expression signature that has a high prognostic significance across MB subgroups.

U2 - 10.1093/neuonc/noaa254

DO - 10.1093/neuonc/noaa254

M3 - SCORING: Journal article

C2 - 33175161

VL - 23

SP - 586

EP - 598

JO - NEURO-ONCOLOGY

JF - NEURO-ONCOLOGY

SN - 1522-8517

IS - 4

ER -