Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps

J Park, RW Wysocki, Z Amoozgar, L Maiorino… - Science translational …, 2016 - science.org
J Park, RW Wysocki, Z Amoozgar, L Maiorino, MR Fein, J Jorns, AF Schott…
Science translational medicine, 2016science.org
Neutrophils, the most abundant type of leukocytes in blood, can form neutrophil extracellular
traps (NETs). These are pathogen-trapping structures generated by expulsion of the
neutrophil's DNA with associated proteolytic enzymes. NETs produced by infection can
promote cancer metastasis. We show that metastatic breast cancer cells can induce
neutrophils to form metastasis-supporting NETs in the absence of infection. Using intravital
imaging, we observed NET-like structures around metastatic 4T1 cancer cells that had …
Neutrophils, the most abundant type of leukocytes in blood, can form neutrophil extracellular traps (NETs). These are pathogen-trapping structures generated by expulsion of the neutrophil’s DNA with associated proteolytic enzymes. NETs produced by infection can promote cancer metastasis. We show that metastatic breast cancer cells can induce neutrophils to form metastasis-supporting NETs in the absence of infection. Using intravital imaging, we observed NET-like structures around metastatic 4T1 cancer cells that had reached the lungs of mice. We also found NETs in clinical samples of triple-negative human breast cancer. The formation of NETs stimulated the invasion and migration of breast cancer cells in vitro. Inhibiting NET formation or digesting NETs with deoxyribonuclease I (DNase I) blocked these processes. Treatment with NET-digesting, DNase I–coated nanoparticles markedly reduced lung metastases in mice. Our data suggest that induction of NETs by cancer cells is a previously unidentified metastasis-promoting tumor-host interaction and a potential therapeutic target.
AAAS