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MYCN Function in Neuroblastoma Development

Dysregulated expression of the transcription factor MYCN is frequently detected in nervous system tumors such as childhood neuroblastoma. Here, gene amplification of MYCN is a single oncogenic driver inducing neoplastic transformation in neural crest-derived cells. This abnormal MYCN expression is o...

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Autores principales: Otte, Jörg, Dyberg, Cecilia, Pepich, Adena, Johnsen, John Inge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873735/
https://www.ncbi.nlm.nih.gov/pubmed/33585251
http://dx.doi.org/10.3389/fonc.2020.624079
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author Otte, Jörg
Dyberg, Cecilia
Pepich, Adena
Johnsen, John Inge
author_facet Otte, Jörg
Dyberg, Cecilia
Pepich, Adena
Johnsen, John Inge
author_sort Otte, Jörg
collection PubMed
description Dysregulated expression of the transcription factor MYCN is frequently detected in nervous system tumors such as childhood neuroblastoma. Here, gene amplification of MYCN is a single oncogenic driver inducing neoplastic transformation in neural crest-derived cells. This abnormal MYCN expression is one of the strongest predictors of poor prognosis. It is present at diagnosis and is never acquired during later tumorigenesis of MYCN non-amplified neuroblastoma. This suggests that increased MYCN expression is an early event in these cancers leading to a peculiar dysregulation of cells that results in embryonal or cancer stem-like qualities, such as increased self-renewal, apoptotic resistance, and metabolic flexibility.
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spelling pubmed-78737352021-02-11 MYCN Function in Neuroblastoma Development Otte, Jörg Dyberg, Cecilia Pepich, Adena Johnsen, John Inge Front Oncol Oncology Dysregulated expression of the transcription factor MYCN is frequently detected in nervous system tumors such as childhood neuroblastoma. Here, gene amplification of MYCN is a single oncogenic driver inducing neoplastic transformation in neural crest-derived cells. This abnormal MYCN expression is one of the strongest predictors of poor prognosis. It is present at diagnosis and is never acquired during later tumorigenesis of MYCN non-amplified neuroblastoma. This suggests that increased MYCN expression is an early event in these cancers leading to a peculiar dysregulation of cells that results in embryonal or cancer stem-like qualities, such as increased self-renewal, apoptotic resistance, and metabolic flexibility. Frontiers Media S.A. 2021-01-27 /pmc/articles/PMC7873735/ /pubmed/33585251 http://dx.doi.org/10.3389/fonc.2020.624079 Text en Copyright © 2021 Otte, Dyberg, Pepich and Johnsen http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Otte, Jörg
Dyberg, Cecilia
Pepich, Adena
Johnsen, John Inge
MYCN Function in Neuroblastoma Development
title MYCN Function in Neuroblastoma Development
title_full MYCN Function in Neuroblastoma Development
title_fullStr MYCN Function in Neuroblastoma Development
title_full_unstemmed MYCN Function in Neuroblastoma Development
title_short MYCN Function in Neuroblastoma Development
title_sort mycn function in neuroblastoma development
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873735/
https://www.ncbi.nlm.nih.gov/pubmed/33585251
http://dx.doi.org/10.3389/fonc.2020.624079
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