Title |
Employing the Myc Transcriptional Network to Reveal Oncogenic Pathways
|
Institution |
FRED HUTCHINSON CANCER RESEARCH CENTER, SEATTLE, WA
|
Principal Investigator |
EISENMAN, ROBERT
|
NCI Program Director |
Mietz
|
Cancer Activity |
DNA Chromosome Aberrations
|
Division |
DCB
|
Funded Amount |
$635,460
|
Project Dates |
09/30/1991 - 06/30/2019
|
Fiscal Year |
2017
|
Project Type |
Grant
|
Research Topics w/ Percent Relevance |
Cancer Types w/ Percent Relevance |
Cancer (100.0%)
Childhood Cancers (50.0%)
|
Brain (100.0%)
Neuroblastoma (50.0%)
|
Research Type |
Cancer Initiation: Alterations in Chromosomes
|
Abstract |
"DESCRIPTION (provided by applicant): The Myc protein family is profoundly involved in initiation, progression, and survival of a wide range of human cancers. Understanding the critical tumor-specific pathways through which Myc drives neoplasia presents a major hurdle in inhibiting Myc-driven cancers. Myc is a transcription factor that forms a heterodimer with the Max protein. The Myc-Max dimer binds DNA and broadly regulates expression of large numbers of genes involved in cell growth and division. When deregulated, Myc-Max alters the levels and timing of gene expression leading to multiple metabolic and growth related changes that support tumor progression. Importantly, recent studies have shown that Myc-Max does not function alone, but is part of a larger ""network"" of protein interactions, the Max/Mlx network. Mlx is a Max-like protein that heterodimerizes with the transcription factors MondoA and ChREBP to regulate genes primarily involved in cell metabolism. The Max and Mlx arms of the network are distinct yet connected. While much research has focused on these transcription factors, we lack a clear understanding of how the extended Max-Mlx network is functionally integrated and what roles this larger network plays in normal cellular processes and tumorigenesis. The objectives of this proposal are to reveal the transcriptional circuitry and the functional dependencies within the Max/Mlx network that enable Myc activity in neoplastic cells. These ideas are based on our preliminary data indicating a specific and critical role for MondoA-Mlx in the metabolism and survival of Myc-driven tumors. These studies reveal cross-talk and functional dependencies among factors within the larger network. The central hypothesis is that the Max and Mlx arms of the network cooperate to link Myc to nutrient sensing thereby serving to augment metabolic flexibility within the evolving tumor. We propose two specific aims: (1) Define the molecular mechanisms through which Myc-induced metabolic reprograming is enabled by the extended Max-Mlx transcription network; (2) Employ mouse genetics to reveal physiological and molecular functions of Mlx and Max. Aim 1 will use metabolomics and ChIP-Seq to define metabolic pathways and genes that are co-regulated by Myc-Max and MondoA-Mlx in human neuroblastomas. This information will in turn be used to identify potential targets for specific inhibitors in a wide spectrum of tumor types. Aim 2 will employ our conditional targeted deletions of mlx and of max to define their roles in lymphoid development, in the etiology of leukemia, and in orchestrating genomic binding by the transcription factors within the extended network. The rationale for the proposal is that it will reveal novel pathways and modes of regulation that will provide us with new and more sensitive targets for tumor therapy. " |