| Literature DB >> 27798263 |
Juwon Park1, Robert W Wysocki1,2,3, Zohreh Amoozgar4, Laura Maiorino1,5, Miriam R Fein1,3, Julie Jorns6, Anne F Schott6, Yumi Kinugasa-Katayama1, Youngseok Lee7, Nam Hee Won7, Elizabeth S Nakasone1,5, Stephen A Hearn8, Victoria Küttner1, Jing Qiu1, Ana S Almeida1, Naiara Perurena1, Kai Kessenbrock9, Michael S Goldberg4,10, Mikala Egeblad11.
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.Entities:
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Year: 2016 PMID: 27798263 PMCID: PMC5550900 DOI: 10.1126/scitranslmed.aag1711
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956