4.4 Review

Cancer clocks in tumourigenesis: the p53 pathway and beyond

Journal

ENDOCRINE-RELATED CANCER
Volume 28, Issue 4, Pages R95-R110

Publisher

BIOSCIENTIFICA LTD
DOI: 10.1530/ERC-20-0475

Keywords

circadian; clock genes; tumourigenesis; mathematical modelling

Funding

  1. WarwickA*STAR Research Attachment Programme (ARAP)
  2. A*STAR Graduate Academy
  3. Warwick University Doctoral College
  4. UK Medical Research Council [MR/N014294/1]
  5. Singapore National Research Foundation's Competitive Research Programme [NRF-CRP17-2017-02]
  6. Singapore National Medical Research Council [NMRC/CIRG/1465/2017]
  7. Warwick Innovation Fund
  8. Cancer Research UK [C53720/A29468]
  9. IMCB core funds

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Circadian rhythms play a significant role in cancer biology, with clock genes impacting tumourigenesis through various pathways. However, the function of the clock can be both pro- and anti-tumourigenic depending on the model and cell type. To fully understand the role of the circadian clock in tumors, analysis of molecular clock status compared to healthy tissue is necessary.
Circadian rhythms regulate a vast array of physiological and cellular processes, as well as the hormonal milieu, to keep our cells synchronised to the light-darkness cycle. Epidemiologic studies have implicated circadian disruption in the development of breast and other cancers, and numerous clock genes are dysregulated in human tumours. Here we review the evidence that circadian rhythms, when altered at the molecular level, influence cancer growth. We also note some common pitfalls in circadian-cancer research and how they might be avoided to maximise comparable results and minimise misleading data. Studies of circadian gene mutant mice, and human cancer models in vitro and in vivo, demonstrate that clock genes can impact tumourigenesis. Clock genes influence important cancer-related pathways, ranging from p53-mediated apoptosis to cell cycle progression. Confusingly, clock dysfunction can be both pro- or anti-tumourigenic in a model and cell type-specific manner. Due to this duality, there is no canonical mechanism for clock interaction with tumourigenic pathways. To understand the role of the circadian clock in patients' tumours requires analysis of the molecular clock status compared to healthy tissue. Novel mathematical approaches are under development, but this remains largely aspirational, and is hampered by a lack of temporal information in publicly available datasets. Current evidence broadly supports the notion that the circadian clock is important for cancer biology. More work is necessary to develop an overarching model of this connection. Future studies would do well to analyse the clock network in addition to alterations in single clock genes.

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