4.8 Article

The metastatic spread of breast cancer accelerates during sleep

期刊

NATURE
卷 607, 期 7917, 页码 156-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-022-04875-y

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资金

  1. European Research Council [101001652]
  2. strategic focus area of Personalized Health and Related Technologies at ETH Zurich [PHRT-541]
  3. Future and Emerging Technologies programme of the European Commission [801159-B2B]
  4. Swiss National Science Foundation [PP00P3_190077]
  5. Swiss Cancer League [KLS-4834-08-2019]
  6. Cantons of Basel through ETH Zurich [PMB-01-16]
  7. University of Basel
  8. Basel Cancer League [KLbB-4763-02-2019]
  9. ETH Zurich
  10. H2020 Marie Skodowska-Curie Actions [101028567]
  11. European Research Council (ERC) [101001652] Funding Source: European Research Council (ERC)
  12. Marie Curie Actions (MSCA) [101028567] Funding Source: Marie Curie Actions (MSCA)
  13. Swiss National Science Foundation (SNF) [PP00P3_190077] Funding Source: Swiss National Science Foundation (SNF)

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The generation of circulating tumor cells (CTCs) with metastatic ability is concentrated during the rest phase, and CTCs generated during the active phase lack metastatic ability. Mechanistically, the upregulation of mitotic genes during the rest phase enables CTCs' metastasis proficiency. Circadian rhythm hormones such as melatonin, testosterone and glucocorticoids dictate the generation dynamics of CTCs, and insulin promotes tumor cell proliferation in a time-dependent manner.
The metastatic spread of cancer is achieved by the haematogenous dissemination of circulating tumour cells (CTCs). Generally, however, the temporal dynamics that dictate the generation of metastasis-competent CTCs are largely uncharacterized, and it is often assumed that CTCs are constantly shed from growing tumours or are shed as a consequence of mechanical insults'. Here we observe a striking and unexpected pattern of CTC generation dynamics in both patients with breast cancer and mouse models, highlighting that most spontaneous CTC intravasation events occur during sleep. Further, we demonstrate that rest-phase CTCs are highly prone to metastasize, whereas CTCs generated during the active phase are devoid of metastatic ability. Mechanistically, single-cell RNA sequencing analysis of CTCs reveals a marked upregulation of mitotic genes exclusively during the rest phase in both patients and mouse models, enabling metastasis proficiency. Systemically, we find that key circadian rhythm hormones such as melatonin, testosterone and glucocorticoids dictate CTC generation dynamics, and as a consequence, that insulin directly promotestumour cell proliferation in vivo, yet in a time-dependent manner. Thus, the spontaneous generation of CTCs with a high proclivity to metastasize does not occur continuously, but it is concentrated within the rest phase of the affected individual, providing a new rationale for time-controlled interrogation and treatment of metastasis-prone cancers.

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