Autophagy promotes the survival of dormant breast cancer cells and metastatic tumour recurrence

Laura Vera-Ramirez, Suman K. Vodnala, Ryan Nini, Kent W. Hunter () and Jeffrey E. Green ()
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Laura Vera-Ramirez: National Cancer Institute, National Institutes of Health
Suman K. Vodnala: National Cancer Institute, National Institutes of Health
Ryan Nini: National Cancer Institute, National Institutes of Health
Kent W. Hunter: National Cancer Institute, National Institutes of Health
Jeffrey E. Green: National Cancer Institute, National Institutes of Health

Nature Communications, 2018, vol. 9, issue 1, 1-12

Abstract: Abstract Cancer recurrence after initial diagnosis and treatment is a major cause of breast cancer (BC) mortality, which results from the metastatic outbreak of dormant tumour cells. Alterations in the tumour microenvironment can trigger signalling pathways in dormant cells leading to their proliferation. However, processes involved in the initial and the long-term survival of disseminated dormant BC cells remain largely unknown. Here we show that autophagy is a critical mechanism for the survival of disseminated dormant BC cells. Pharmacologic or genetic inhibition of autophagy in dormant BC cells results in significantly decreased cell survival and metastatic burden in mouse and human 3D in vitro and in vivo preclinical models of dormancy. In vivo experiments identify autophagy gene autophagy-related 7 (ATG7) to be essential for autophagy activation. Mechanistically, inhibition of the autophagic flux in dormant BC cells leads to the accumulation of damaged mitochondria and reactive oxygen species (ROS), resulting in cell apoptosis.

Date: 2018
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DOI: 10.1038/s41467-018-04070-6

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