The MYC transcription factor network: balancing metabolism, proliferation and oncogenesis.
10.1007/s11684-018-0650-z
- Author:
Patrick A CARROLL
1
;
Brian W FREIE
1
;
Haritha MATHSYARAJA
1
;
Robert N EISENMAN
2
Author Information
1. Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA, 90109, USA.
2. Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA, 90109, USA. eisenman@fhcrc.org.
- Publication Type:Journal Article
- Keywords:
MAX;
MLX;
MYC;
cancer;
network;
transcription
- MeSH:
Animals;
Carcinogenesis;
metabolism;
Disease Progression;
Gene Expression Regulation;
Gene Regulatory Networks;
physiology;
Humans;
Protein Interaction Domains and Motifs;
physiology;
Proto-Oncogene Proteins c-myc;
metabolism
- From:
Frontiers of Medicine
2018;12(4):412-425
- CountryChina
- Language:English
-
Abstract:
Transcription factor networks have evolved in order to control, coordinate, and separate, the functions of distinct network modules spatially and temporally. In this review we focus on the MYC network (also known as the MAX-MLX Network), a highly conserved super-family of related basic-helix-loop-helix-zipper (bHLHZ) proteins that functions to integrate extracellular and intracellular signals and modulate global gene expression. Importantly the MYC network has been shown to be deeply involved in a broad spectrum of human and other animal cancers. Here we summarize molecular and biological properties of the network modules with emphasis on functional interactions among network members. We suggest that these network interactions serve to modulate growth and metabolism at the transcriptional level in order to balance nutrient demand with supply, to maintain growth homeostasis, and to influence cell fate. Moreover, oncogenic activation of MYC and/or loss of a MYC antagonist, results in an imbalance in the activity of the network as a whole, leading to tumor initiation, progression and maintenance.
