Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps

Juwon Park(Cold Spring Harbor Laboratory), Robert W. Wysocki(Cold Spring Harbor Laboratory), Zohreh Amoozgar(Dana-Farber Cancer Institute), Laura Maiorino(Cold Spring Harbor Laboratory), Miriam R. Fein(Cold Spring Harbor Laboratory), Julie M. Jorns(University of Michigan), Anne F. Schott(University of Michigan), Yumi Kinugasa‐Katayama(Cold Spring Harbor Laboratory), Youngseok Lee(Korea University Medical Center), Nam Hee Won(Korea University Medical Center), Elizabeth S. Nakasone(Cold Spring Harbor Laboratory), Stephen Hearn(Cold Spring Harbor Laboratory), Victoria Küttner(Cold Spring Harbor Laboratory), Jing Qiu(Cold Spring Harbor Laboratory), Ana S. Almeida(Cold Spring Harbor Laboratory), Naiara Perurena(Cold Spring Harbor Laboratory), Kai Kessenbrock(University of California, Irvine), Michael S. Goldberg(Harvard University), Mikala Egeblad(Cold Spring Harbor Laboratory)
Science Translational Medicine
October 19, 2016
Cited by 977Open Access
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Abstract

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.


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