Impact of Simulated Rotating Shift Work on Mammary Tumor Development in the p53R270H©/+WAPCre Mouse Model for Breast Cancer

Author:

Streng Astrid A.12,Van Dycke Kirsten C. G.12,van Oostrom Conny T. M.2,Salvatori Daniela C. F.34,Hulsegge Gerben5,Chaves Inês1,Roenneberg Till6,Zander Serge A. L.3ORCID,van Steeg Harry2,van der Horst Gijsbertus T. J.1,van Kerkhof Linda W. M.2

Affiliation:

1. Department of Molecular Genetics, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands

2. Centre for Health Protection, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands

3. Experimental Pathology Services Lab, Central Laboratory Animal Facility, Leiden University Medical Center, Leiden, The Netherlands

4. Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands

5. Sustainable Productivity and Employability, Netherlands Organization for Applied Scientific Research (TNO), Leiden, The Netherlands

6. Institute of Medical Psychology, Ludwig-Maximilians-University, Munich, Germany

Abstract

Epidemiological studies associate night shift work with increased breast cancer risk. However, the underlying mechanisms are not clearly understood. To better understand these mechanisms, animal models that mimic the human situation of different aspects of shift work are needed. In this study, we used “timed sleep restriction” (TSR) cages to simulate clockwise and counterclockwise rotating shift work schedules and investigated predicted sleep patterns and mammary tumor development in breast tumor–prone female p53R270H©/+ WAPCre mice. We show that TSR cages are effective in disturbing normal activity and estimated sleep patterns. Although circadian rhythms were not shifted, we observed effects of the rotating schedules on sleep timing and sleep duration. Sleep loss during a simulated shift was partly compensated after the shift and also partly during the free days. No effects were observed on body weight gain and latency time of breast cancer development. In summary, our study shows that the TSR cages can be used to model shift work in mice and affect patterns of activity and sleep. The effect of disturbing sleep patterns on carcinogenesis needs to be further investigated.

Publisher

SAGE Publications

Subject

Physiology (medical),Physiology

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