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Circadian and melatonin disruption by exposure to light at night drives intrinsic resistance to tamoxifen therapy in breast cancer.

Abstract
Resistance to endocrine therapy is a major impediment to successful treatment of breast cancer. Preclinical and clinical evidence links resistance to antiestrogen drugs in breast cancer cells with the overexpression and/or activation of various pro-oncogenic tyrosine kinases. Disruption of circadian rhythms by night shift work or disturbed sleep-wake cycles may lead to an increased risk of breast cancer and other diseases. Moreover, light exposure at night (LEN) suppresses the nocturnal production of melatonin that inhibits breast cancer growth. In this study, we used a rat model of estrogen receptor (ERĪ±(+)) MCF-7 tumor xenografts to demonstrate how altering light/dark cycles with dim LEN (dLEN) speed the development of breast tumors, increasing their metabolism and growth and conferring an intrinsic resistance to tamoxifen therapy. These characteristics were not observed in animals in which the circadian melatonin rhythm was not disrupted, or in animals subjected to dLEN if they received nocturnal melatonin replacement. Strikingly, our results also showed that melatonin acted both as a tumor metabolic inhibitor and a circadian-regulated kinase inhibitor to reestablish the sensitivity of breast tumors to tamoxifen and tumor regression. Together, our findings show how dLEN-mediated disturbances in nocturnal melatonin production can render tumors insensitive to tamoxifen.
AuthorsRobert T Dauchy, Shulin Xiang, Lulu Mao, Samantha Brimer, Melissa A Wren, Lin Yuan, Muralidharan Anbalagan, Adam Hauch, Tripp Frasch, Brian G Rowan, David E Blask, Steven M Hill
JournalCancer research (Cancer Res) Vol. 74 Issue 15 Pg. 4099-110 (Aug 01 2014) ISSN: 1538-7445 [Electronic] United States
PMID25062775 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright©2014 American Association for Cancer Research.
Chemical References
  • Antineoplastic Agents, Hormonal
  • Tamoxifen
  • Melatonin
Topics
  • Animals
  • Antineoplastic Agents, Hormonal (pharmacology)
  • Breast Neoplasms (blood, drug therapy, pathology)
  • Circadian Rhythm (physiology)
  • Disease Models, Animal
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Light
  • MCF-7 Cells
  • Melatonin (blood)
  • Mice, Nude
  • Random Allocation
  • Rats
  • Tamoxifen (pharmacology)
  • Xenograft Model Antitumor Assays

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