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Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps

Authors
Park, JuwonWysocki, Robert W.Amoozgar, ZohrehMaiorino, LauraFein, Miriam R.Jorns, JulieSchott, Anne F.Kinugasa-Katayama, YumiLee, YoungseokNam Hee WonNakasone, Elizabeth S.Hearn, Stephen A.Kuettner, VictoriaQiu, JingAlmeida, Ana S.Perurena, NaiaraKessenbrock, KaiGoldberg, Michael S.Egeblad, Mikala
Issue Date
19-10월-2016
Publisher
AMER ASSOC ADVANCEMENT SCIENCE
Citation
SCIENCE TRANSLATIONAL MEDICINE, v.8, no.361
Indexed
SCIE
SCOPUS
Journal Title
SCIENCE TRANSLATIONAL MEDICINE
Volume
8
Number
361
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/87162
DOI
10.1126/scitranslmed.aag1711
ISSN
1946-6234
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 metastasispromoting tumor-host interaction and a potential therapeutic target.
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