MYC Ran Up the Clock: The Complex Interplay between MYC and the Molecular Circadian Clock in Cancer.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
20 Jul 2021
Historique:
received: 01 06 2021
revised: 02 07 2021
accepted: 14 07 2021
entrez: 24 7 2021
pubmed: 25 7 2021
medline: 5 8 2021
Statut: epublish

Résumé

The MYC oncoprotein and its family members N-MYC and L-MYC are known to drive a wide variety of human cancers. Emerging evidence suggests that MYC has a bi-directional relationship with the molecular clock in cancer. The molecular clock is responsible for circadian (~24 h) rhythms in most eukaryotic cells and organisms, as a mechanism to adapt to light/dark cycles. Disruption of human circadian rhythms, such as through shift work, may serve as a risk factor for cancer, but connections with oncogenic drivers such as MYC were previously not well understood. In this review, we examine recent evidence that MYC in cancer cells can disrupt the molecular clock; and conversely, that molecular clock disruption in cancer can deregulate and elevate MYC. Since MYC and the molecular clock control many of the same processes, we then consider competition between MYC and the molecular clock in several select aspects of tumor biology, including chromatin state, global transcriptional profile, metabolic rewiring, and immune infiltrate in the tumor. Finally, we discuss how the molecular clock can be monitored or diagnosed in human tumors, and how MYC inhibition could potentially restore molecular clock function. Further study of the relationship between the molecular clock and MYC in cancer may reveal previously unsuspected vulnerabilities which could lead to new treatment strategies.

Identifiants

pubmed: 34299381
pii: ijms22147761
doi: 10.3390/ijms22147761
pmc: PMC8305799
pii:
doi:

Substances chimiques

Chromatin 0
Period Circadian Proteins 0
Proto-Oncogene Proteins c-myc 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wilmot Cancer Institute
ID : None
Organisme : NCI NIH HHS
ID : NCI UG1CA189961-07S1
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM135134
Pays : United States
Organisme : NCI NIH HHS
ID : R00 CA204593
Pays : United States
Organisme : NCI NIH HHS
ID : R00CA204593
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32GM135134
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189961
Pays : United States

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Auteurs

Jamison B Burchett (JB)

Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.

Amelia M Knudsen-Clark (AM)

Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA.

Brian J Altman (BJ)

Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY 14642, USA.

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