Evidence map›Paper›PMID 34299381›Full record

ReviewInternational journal of molecular sciences2021

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

Jamison B Burchett, Amelia M Knudsen-Clark, Brian J Altman

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  17. Review
  18. Circadian GeneInternational journal of molecular sciences · 2022
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Jamison B BurchettDepartment of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Amelia M Knudsen-ClarkDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA.ORCID 0000-0002-1685-9413
Brian J AltmanDepartment of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.ORCID 0000-0002-3954-4916
University of Rochester Medical Center · US

Funding

URCC NCORP Research BaseUG1CA189961 · NCI · UNIVERSITY OF ROCHESTER · PI Michelle C Janelsins, KAREN M. MUSTIAN · 2014 to 2026
$67.7M
Training in Wellness and Resiliency at the University of Rochester Medical Center and College of Arts, Sciences & EngineeringT32GM135134 · NIGMS · UNIVERSITY OF ROCHESTER · PI Jeffrey J Hayes, Lynne E Maquat · 2020 to 2026
$2.9M
Oncogenic Disruption of the Circadian Metabolic Cycle in CancerR00CA204593 · NCI · UNIVERSITY OF ROCHESTER · PI ALTMAN, BRIAN JAMES · 2018 to 2020
$747k
NCI NIH HHS NCI UG1CA189961-07S1NCI NIH HHS R00 CA204593NCI NIH HHS R00CA204593NCI NIH HHS UG1 CA189961NIGMS NIH HHS T32 GM135134NIGMS NIH HHS T32GM135134Wilmot Cancer Institute None
6 · The paper itself

Abstract

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.

Indexed as

AnimalsCarcinogenesisChromatinCircadian ClocksCircadian RhythmHumansNeoplasmsPeriod Circadian ProteinsProto-Oncogene Proteins c-mycTranscription, GeneticChromatinPeriod Circadian ProteinsProto-Oncogene Proteins c-myccancercancer metabolismchromatincircadian rhythmcomputational biologymolecular clockMYCpause releasetranscription factortumor immunology

Identifiers

PMID34299381
PMCPMC8305799
OpenAlexW3186727325

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.