MYCN in Neuroblastoma: “Old Wine into New Wineskins”

MYCN Proto-Oncogene, BHLH Transcription Factor (MYCN) has been one of the most studied genes in neuroblastoma. It is known for its oncogenetic mechanisms, as well as its role in the prognosis of the disease and it is considered one of the prominent targets for neuroblastoma therapy. In the present w...

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Main Authors: Maria Braoudaki, Kyriaki Hatziagapiou, Apostolos Zaravinos, George I. Lambrou
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Diseases
Subjects:
Online Access:https://www.mdpi.com/2079-9721/9/4/78
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author Maria Braoudaki
Kyriaki Hatziagapiou
Apostolos Zaravinos
George I. Lambrou
author_facet Maria Braoudaki
Kyriaki Hatziagapiou
Apostolos Zaravinos
George I. Lambrou
author_sort Maria Braoudaki
collection DOAJ
description MYCN Proto-Oncogene, BHLH Transcription Factor (MYCN) has been one of the most studied genes in neuroblastoma. It is known for its oncogenetic mechanisms, as well as its role in the prognosis of the disease and it is considered one of the prominent targets for neuroblastoma therapy. In the present work, we attempted to review the literature, on the relation between MYCN and neuroblastoma from all possible mechanistic sites. We have searched the literature for the role of MYCN in neuroblastoma based on the following topics: the references of MYCN in the literature, the gene’s anatomy, along with its transcripts, the protein’s anatomy, the epigenetic mechanisms regulating MYCN expression and function, as well as MYCN amplification. <i>MYCN</i> plays a significant role in neuroblastoma biology. Its functions and properties range from the forming of G-quadraplexes, to the interaction with miRNAs, as well as the regulation of gene methylation and histone acetylation and deacetylation. Although <i>MYCN</i> is one of the most primary genes studied in neuroblastoma, there is still a lot to be learned. Our knowledge on the exact mechanisms of MYCN amplification, etiology and potential interventions is still limited. The knowledge on the molecular mechanisms of MYCN in neuroblastoma, could have potential prognostic and therapeutic advantages.
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spelling doaj.art-6b225569d0d7427691b427de268eae0e2023-11-23T07:55:48ZengMDPI AGDiseases2079-97212021-10-01947810.3390/diseases9040078MYCN in Neuroblastoma: “Old Wine into New Wineskins”Maria Braoudaki0Kyriaki Hatziagapiou1Apostolos Zaravinos2George I. Lambrou3Department of Life and Environmental Sciences, School of Life and Health Sciences, University of Hertfordshire, Hatfield AL10 9AB, Hertfordshire, UKChoremeio Research Laboratory, First Department of Pediatrics, National and Kapodistrian University of Athens, Thivon & Levadeias 8, Goudi, 11527 Athens, GreeceDepartment of Life Sciences, European University Cyprus, Diogenis Str., 6, Nicosia 2404, CyprusChoremeio Research Laboratory, First Department of Pediatrics, National and Kapodistrian University of Athens, Thivon & Levadeias 8, Goudi, 11527 Athens, GreeceMYCN Proto-Oncogene, BHLH Transcription Factor (MYCN) has been one of the most studied genes in neuroblastoma. It is known for its oncogenetic mechanisms, as well as its role in the prognosis of the disease and it is considered one of the prominent targets for neuroblastoma therapy. In the present work, we attempted to review the literature, on the relation between MYCN and neuroblastoma from all possible mechanistic sites. We have searched the literature for the role of MYCN in neuroblastoma based on the following topics: the references of MYCN in the literature, the gene’s anatomy, along with its transcripts, the protein’s anatomy, the epigenetic mechanisms regulating MYCN expression and function, as well as MYCN amplification. <i>MYCN</i> plays a significant role in neuroblastoma biology. Its functions and properties range from the forming of G-quadraplexes, to the interaction with miRNAs, as well as the regulation of gene methylation and histone acetylation and deacetylation. Although <i>MYCN</i> is one of the most primary genes studied in neuroblastoma, there is still a lot to be learned. Our knowledge on the exact mechanisms of MYCN amplification, etiology and potential interventions is still limited. The knowledge on the molecular mechanisms of MYCN in neuroblastoma, could have potential prognostic and therapeutic advantages.https://www.mdpi.com/2079-9721/9/4/78MYCNamplificationepigenetic regulationacetylationG-quadraplexneuroblastoma
spellingShingle Maria Braoudaki
Kyriaki Hatziagapiou
Apostolos Zaravinos
George I. Lambrou
MYCN in Neuroblastoma: “Old Wine into New Wineskins”
Diseases
MYCN
amplification
epigenetic regulation
acetylation
G-quadraplex
neuroblastoma
title MYCN in Neuroblastoma: “Old Wine into New Wineskins”
title_full MYCN in Neuroblastoma: “Old Wine into New Wineskins”
title_fullStr MYCN in Neuroblastoma: “Old Wine into New Wineskins”
title_full_unstemmed MYCN in Neuroblastoma: “Old Wine into New Wineskins”
title_short MYCN in Neuroblastoma: “Old Wine into New Wineskins”
title_sort mycn in neuroblastoma old wine into new wineskins
topic MYCN
amplification
epigenetic regulation
acetylation
G-quadraplex
neuroblastoma
url https://www.mdpi.com/2079-9721/9/4/78
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AT apostoloszaravinos mycninneuroblastomaoldwineintonewwineskins
AT georgeilambrou mycninneuroblastomaoldwineintonewwineskins