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Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma

Medulloblastoma, the most common pediatric malignant brain tumor, continues to have a high rate of morbidity and mortality in childhood. Recent advances in cancer genomics, single-cell sequencing, and sophisticated tumor models have revolutionized the characterization and stratification of medullobl...

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Autores principales: Zou, Han, Poore, Brad, Broniscer, Alberto, Pollack, Ian F., Hu, Baoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139663/
https://www.ncbi.nlm.nih.gov/pubmed/32164294
http://dx.doi.org/10.3390/cancers12030643
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author Zou, Han
Poore, Brad
Broniscer, Alberto
Pollack, Ian F.
Hu, Baoli
author_facet Zou, Han
Poore, Brad
Broniscer, Alberto
Pollack, Ian F.
Hu, Baoli
author_sort Zou, Han
collection PubMed
description Medulloblastoma, the most common pediatric malignant brain tumor, continues to have a high rate of morbidity and mortality in childhood. Recent advances in cancer genomics, single-cell sequencing, and sophisticated tumor models have revolutionized the characterization and stratification of medulloblastoma. In this review, we discuss heterogeneity associated with four major subgroups of medulloblastoma (WNT, SHH, Group 3, and Group 4) on the molecular and cellular levels, including histological features, genetic and epigenetic alterations, proteomic landscape, cell-of-origin, tumor microenvironment, and therapeutic approaches. The intratumoral molecular heterogeneity and intertumoral cellular diversity clearly underlie the divergent biology and clinical behavior of these lesions and highlight the future role of precision treatment in this devastating brain tumor in children.
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spelling pubmed-71396632020-04-10 Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma Zou, Han Poore, Brad Broniscer, Alberto Pollack, Ian F. Hu, Baoli Cancers (Basel) Review Medulloblastoma, the most common pediatric malignant brain tumor, continues to have a high rate of morbidity and mortality in childhood. Recent advances in cancer genomics, single-cell sequencing, and sophisticated tumor models have revolutionized the characterization and stratification of medulloblastoma. In this review, we discuss heterogeneity associated with four major subgroups of medulloblastoma (WNT, SHH, Group 3, and Group 4) on the molecular and cellular levels, including histological features, genetic and epigenetic alterations, proteomic landscape, cell-of-origin, tumor microenvironment, and therapeutic approaches. The intratumoral molecular heterogeneity and intertumoral cellular diversity clearly underlie the divergent biology and clinical behavior of these lesions and highlight the future role of precision treatment in this devastating brain tumor in children. MDPI 2020-03-10 /pmc/articles/PMC7139663/ /pubmed/32164294 http://dx.doi.org/10.3390/cancers12030643 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zou, Han
Poore, Brad
Broniscer, Alberto
Pollack, Ian F.
Hu, Baoli
Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma
title Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma
title_full Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma
title_fullStr Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma
title_full_unstemmed Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma
title_short Molecular Heterogeneity and Cellular Diversity: Implications for Precision Treatment in Medulloblastoma
title_sort molecular heterogeneity and cellular diversity: implications for precision treatment in medulloblastoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139663/
https://www.ncbi.nlm.nih.gov/pubmed/32164294
http://dx.doi.org/10.3390/cancers12030643
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