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Controlling the Master: Chromatin Dynamics at the MYC Promoter Integrate Developmental Signaling
Olga Zaytseva1,2, Leonie M Quinn3,4
1ACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT 2600, Australia. olga.zaytseva@anu.edu.au.
Abstract:
The transcription factor and cell growth regulator MYC is potently oncogenic and estimated to contribute to most cancers. Decades of attempts to therapeutically target MYC directly have not resulted in feasible clinical applications, and efforts have moved toward indirectly targeting MYC expression, function and/or activity to treat MYC-driven cancer. A multitude of developmental and growth signaling pathways converge on the MYC promoter to modulate transcription through their downstream effectors. Critically, even small increases in MYC abundance (<2 fold) are sufficient to drive overproliferation; however, the details of how oncogenic/growth signaling networks regulate MYC at the level of transcription remain nebulous even during normal development. It is therefore essential to first decipher mechanisms of growth signal-stimulated MYC transcription using in vivo models, with intact signaling environments, to determine exactly how these networks are dysregulated in human cancer. This in turn will provide new modalities and approaches to treat MYC-driven malignancy. Drosophila genetic studies have shed much light on how complex networks signal to transcription factors and enhancers to orchestrate Drosophila MYC (dMYC) transcription, and thus growth and patterning of complex multicellular tissue and organs. This review will discuss the many pathways implicated in patterning MYC transcription during development and the molecular events at the MYC promoter that link signaling to expression. Attention will also be drawn to parallels between mammalian and fly regulation of MYC at the level of transcription.
Insights
Understanding how MYC, a key cancer gene, is regulated by growth signals is crucial for developing new cancer therapies. This review explores how signaling pathways control MYC transcription in development and cancer.
Area of Science:
- Molecular Biology
- Developmental Biology
- Cancer Biology
Background:
- The MYC gene is a potent oncogene implicated in most human cancers.
- Directly targeting MYC has proven clinically challenging, shifting focus to indirect therapeutic strategies.
- Dysregulated MYC expression drives cancer cell proliferation, but the precise transcriptional regulation by growth signals remains unclear.
Purpose of the Study:
- To elucidate the mechanisms of growth signal-stimulated MYC transcription in vivo.
- To understand how signaling networks regulate MYC during normal development and in cancer.
- To identify novel therapeutic targets for MYC-driven malignancies.
Main Methods:
- Review of genetic studies in Drosophila to understand signaling networks and transcription factor regulation.
- Analysis of molecular events at the MYC promoter linking signaling pathways to gene expression.
- Comparison of MYC transcriptional regulation between Drosophila and mammalian systems.
Main Results:
- Growth signaling pathways converge on the MYC promoter to modulate its transcription.
- Even minor increases in MYC levels (<2 fold) drive cellular overproliferation.
- Drosophila studies provide insights into conserved mechanisms of MYC regulation.
Conclusions:
- Deciphering MYC transcriptional regulation is essential for developing effective cancer treatments.
- Understanding developmental signaling provides a framework for investigating MYC dysregulation in cancer.
- Parallels in MYC regulation between flies and mammals offer conserved therapeutic targets.
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