Disrupted circadian clocks and altered tissue mechanics in primary human breast tumours

Research output: Contribution to journalArticle

  • External authors:
  • Eleanor Broadberry
  • Jack Williams
  • Nan Yang
  • Egor Zindy
  • Angela Leek
  • Rachel Waddington
  • Leena Joseph
  • Miles Howe
  • Charles H Streuli

Abstract

Background

Circadian rhythms maintain tissue homeostasis during the 24-h day-night cycle. Cell-autonomous circadian clocks play fundamental roles in cell division, DNA damage responses and metabolism. Circadian disruptions have been proposed as a contributing factor for cancer initiation and progression, although definitive evidence for altered molecular circadian clocks in cancer is still lacking. In this study, we looked at circadian clocks in breast cancer.

Methods

We isolated primary tumours and normal tissues from the same individuals who had developed breast cancer with no metastases. We assessed circadian clocks within primary cells of the patients by lentiviral expression of circadian reporters, and the levels of clock genes in tissues by qPCR. We histologically examined collagen organisation within the normal and tumour tissue areas, and probed the stiffness of the stroma adjacent to normal and tumour epithelium using atomic force microscopy.

Results

Epithelial ducts were disorganised within the tumour areas. Circadian clocks were altered in cultured tumour cells. Tumour regions were surrounded by stroma with an altered collagen organisation and increased stiffness. Levels of Bmal1 messenger RNA (mRNA) were significantly altered in the tumours in comparison to normal epithelia.

Conclusion

Circadian rhythms are suppressed in breast tumour epithelia in comparison to the normal epithelia in paired patient samples. This correlates with increased tissue stiffness around the tumour region. We suggest possible involvement of altered circadian clocks in the development and progression of breast cancer.

Bibliographical metadata

Original languageEnglish
JournalBreast Cancer Research
Volume20
Issue number1
Early online date22 Oct 2018
DOIs
Publication statusPublished - 2018

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