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MYCN and Metabolic Reprogramming in Neuroblastoma

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2022 Sep 9
PMID 36077650
Authors
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Abstract

Neuroblastoma is a pediatric cancer responsible for approximately 15% of all childhood cancer deaths. Aberrant MYCN activation, as a result of genomic amplification, is a major driver of high-risk neuroblastoma, which has an overall survival rate of less than 50%, despite the best treatments currently available. Metabolic reprogramming is an integral part of the growth-promoting program driven by MYCN, which fuels cell growth and proliferation by increasing the uptake and catabolism of nutrients, biosynthesis of macromolecules, and production of energy. This reprogramming process also generates metabolic vulnerabilities that can be exploited for therapy. In this review, we present our current understanding of metabolic reprogramming in neuroblastoma, focusing on transcriptional regulation as a key mechanism in driving the reprogramming process. We also highlight some important areas that need to be explored for the successful development of metabolism-based therapy against high-risk neuroblastoma.

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References
1.
Wang W, Wu Z, Dai Z, Yang Y, Wang J, Wu G . Glycine metabolism in animals and humans: implications for nutrition and health. Amino Acids. 2013; 45(3):463-77. DOI: 10.1007/s00726-013-1493-1. View

2.
Grandori C, Cowley S, James L, Eisenman R . The Myc/Max/Mad network and the transcriptional control of cell behavior. Annu Rev Cell Dev Biol. 2000; 16:653-99. DOI: 10.1146/annurev.cellbio.16.1.653. View

3.
Alborzinia H, Florez A, Kreth S, Bruckner L, Yildiz U, Gartlgruber M . MYCN mediates cysteine addiction and sensitizes neuroblastoma to ferroptosis. Nat Cancer. 2022; 3(4):471-485. PMC: 9050595. DOI: 10.1038/s43018-022-00355-4. View

4.
Choi B, Coloff J . The Diverse Functions of Non-Essential Amino Acids in Cancer. Cancers (Basel). 2019; 11(5). PMC: 6562791. DOI: 10.3390/cancers11050675. View

5.
Ameri K, Harris A . Activating transcription factor 4. Int J Biochem Cell Biol. 2007; 40(1):14-21. DOI: 10.1016/j.biocel.2007.01.020. View