Neutrophil extracellular traps in cancer progression

被引:210
作者
Cools-Lartigue, Jonathan [1 ]
Spicer, Jonathan [1 ]
Najmeh, Sara [1 ]
Ferri, Lorenzo [1 ]
机构
[1] McGill Univ, Dept Surg, LD MacLean Surg Res Labs, Montreal, PQ H3A 2T5, Canada
关键词
Neutrophil extracellular traps; Neutrophil; Cancer; Metastatis; Inflammation; CIRCULATING TUMOR-CELLS; ELASTASE-MEDIATED DEGRADATION; CATHEPSIN-G; COLORECTAL-CANCER; ESOPHAGEAL CANCER; LIVER METASTASIS; ANGIOGENIC SWITCH; SERINE-PROTEASE; CARCINOMA CELLS; INNATE IMMUNITY;
D O I
10.1007/s00018-014-1683-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neutrophils are being increasingly recognized as an important element in tumor progression. They have been shown to exert important effects at nearly every stage of tumor progression with a number of studies demonstrating that their presence is critical to tumor development. Novel aspects of neutrophil biology have recently been elucidated and its contribution to tumorigenesis is only beginning to be appreciated. Neutrophil extracellular traps (NETs) are neutrophil-derived structures composed of DNA decorated with antimicrobial peptides. They have been shown to trap and kill microorganisms, playing a critical role in host defense. However, their contribution to tumor development and metastasis has recently been demonstrated in a number of studies highlighting NETs as a potentially important therapeutic target. Here, studies implicating NETs as facilitators of tumor progression and metastasis are reviewed. In addition, potential mechanisms by which NETs may exert these effects are explored. Finally, the ability to target NETs therapeutically in human neoplastic disease is highlighted.
引用
收藏
页码:4179 / 4194
页数:16
相关论文
共 107 条
[11]   The historical milestones in the understanding of leukocyte biology initiated by Elie Metchnikoff [J].
Cavaillon, Jean-Marc .
JOURNAL OF LEUKOCYTE BIOLOGY, 2011, 90 (03) :413-424
[12]  
Chen L, 2001, EUR J IMMUNOL, V31, P265, DOI 10.1002/1521-4141(200101)31:1<265::AID-IMMU265>3.0.CO
[13]  
2-L
[14]   Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood [J].
Clark, Stephen R. ;
Ma, Adrienne C. ;
Tavener, Samantha A. ;
McDonald, Braedon ;
Goodarzi, Zahra ;
Kelly, Margaret M. ;
Patel, Kamala D. ;
Chakrabarti, Subhadeep ;
McAvoy, Erin ;
Sinclair, Gary D. ;
Keys, Elizabeth M. ;
Allen-Vercoe, Emma ;
DeVinney, Rebekah ;
Doig, Christopher J. ;
Green, Francis H. Y. ;
Kubes, Paul .
NATURE MEDICINE, 2007, 13 (04) :463-469
[15]  
COLOTTA F, 1992, BLOOD, V80, P2012
[16]   Cancer-related inflammation, the seventh hallmark of cancer: links to genetic instability [J].
Colotta, Francesco ;
Allavena, Paola ;
Sica, Antonio ;
Garlanda, Cecilia ;
Mantovani, Alberto .
CARCINOGENESIS, 2009, 30 (07) :1073-1081
[17]   Neutrophil extracellular traps sequester circulating tumor cells and promote metastasis [J].
Cools-Lartigue, Jonathan ;
Spicer, Jonathan ;
McDonald, Braedon ;
Gowing, Stephen ;
Chow, Simon ;
Giannias, Betty ;
Bourdeau, France ;
Kubes, Paul ;
Ferri, Lorenzo .
JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (08) :3446-3458
[18]   MMP-9 supplied by bone marrow-derived cells contributes to skin carcinogenesis [J].
Coussens, LM ;
Tinkle, CL ;
Hanahan, D ;
Werb, Z .
CELL, 2000, 103 (03) :481-490
[19]   Use of Ly6G-specific monoclonal antibody to deplete neutrophils in mice [J].
Daley, Jean M. ;
Thomay, Alan A. ;
Connolly, Michael D. ;
Reichner, Jonathan S. ;
Albina, Jorge E. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2008, 83 (01) :64-70
[20]   Recombinant human Dnase I (rhDNase) in patients with lupus nephritis [J].
Davis, JC ;
Manzi, S ;
Yarboro, C ;
Rairie, J ;
Mcinnes, I ;
Averthelyi, D ;
Sinicropi, D ;
Hale, VG ;
Balow, J ;
Austin, H ;
Boumpas, DT ;
Klippel, JH .
LUPUS, 1999, 8 (01) :68-76