Neutrophils as a Therapeutic Target in Cancer

被引:84
作者
Granot, Zvi [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Inst Med Res Israel Canada, Dept Dev Biol & Canc Res, Jerusalem, Israel
关键词
neutrophils; cancer; metastasis; tumor microenvironment; therapy; TUMOR-ASSOCIATED NEUTROPHILS; SUPPRESSOR-CELLS; POLYMORPHONUCLEAR NEUTROPHILS; MECHANISMS; RESPONSES; PEPTIDES; ARGININE; BLOOD; MET;
D O I
10.3389/fimmu.2019.01710
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neutrophils are the most abundant population of white blood cells in the human circulation. They are terminally differentiated myeloid cells which were traditionally associated with fighting infections and inflammatory processes. While this perception of neutrophils is still widely prevalent, in the past decade it has become clear that neutrophils also play a critical role in tumor growth and progression. The unique tumor microenvironment, consisting of the non-malignant stroma that surrounds tumor cells, is shaped by numerous cues emanating from both tumor cells and stromal cells which support the growing tumor. Various immune cells, including neutrophils, make up a significant proportion of the tumor stroma. Immune cells exist for the protection of the host against various threats including the detection and elimination of cancerous cells. However, in the context of cancer immune cells are often coerced into a tumor supportive phenotype. This is also the case for neutrophils, which are often described to possess tumor promoting properties and to associate with poorer prognosis. The fact that neutrophils may contribute to tumor growth and progression suggests they may be targets for anti-cancer therapies. This review discusses the various functions neutrophils may play in cancer and the possibility of targeting these functions as a novel mode of immunotherapy.
引用
收藏
页数:6
相关论文
共 44 条
[1]   Neutrophil extracellular traps produced during inflammation awaken dormant cancer cells in mice [J].
Albrengues, Jean ;
Shields, Mario A. ;
Ng, David ;
Park, Chun Gwon ;
Ambrico, Alexandra ;
Poindexter, Morgan E. ;
Upadhyay, Priya ;
Uyeminami, Dale L. ;
Pommier, Arnaud ;
Kuttner, Victoria ;
Bruzas, Emilis ;
Maiorino, Laura ;
Bautista, Carmelita ;
Carmona, Ellese M. ;
Gimotty, Phyllis A. ;
Fearon, Douglas T. ;
Chang, Kenneth ;
Lyons, Scott K. ;
Pinkerton, Kent E. ;
Trotman, Lloyd C. ;
Goldberg, Michael S. ;
Yeh, Johannes T. -H. ;
Egeblad, Mikala .
SCIENCE, 2018, 361 (6409) :1353-+
[2]   Prognostic value of intratumoral neutrophils in advanced gastric carcinoma in a high-risk area in northern Italy [J].
Caruso, RA ;
Bellocco, R ;
Pagano, M ;
Bertoli, G ;
Rigoli, L ;
Inferrera, C .
MODERN PATHOLOGY, 2002, 15 (08) :831-837
[3]   QUANTITATIVE STUDIES OF BLOOD AND BONE MARROW NEUTROPHILS IN NORMAL MICE [J].
CHERVENICK, PA ;
BOGGS, DR ;
MARSH, JC ;
CARTWRIGHT, GE ;
WINTROBE, MM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1968, 215 (02) :353-+
[4]   Neutrophils in cancer: neutral no more [J].
Coffelt, Seth B. ;
Wellenstein, Max D. ;
de Visser, Karin E. .
NATURE REVIEWS CANCER, 2016, 16 (07) :431-446
[5]   Lectin-type oxidized LDL receptor-1 distinguishes population of human polymorphonuclear myeloid-derived suppressor cells in cancer patients [J].
Condamine, Thomas ;
Dominguez, George A. ;
Youn, Je-In ;
Kossenkov, Andrew V. ;
Mony, Sridevi ;
Alicea-Torres, Kevin ;
Tcyganov, Evgenii ;
Hashimoto, Ayumi ;
Nefedova, Yulia ;
Lin, Cindy ;
Partlova, Simona ;
Garfall, Alfred ;
Vogl, Dan T. ;
Xu, Xiaowei ;
Knight, Stella C. ;
Malietzis, George ;
Lee, Gui Han ;
Eruslanov, Evgeniy ;
Albelda, Steven M. ;
Wang, Xianwei ;
Mehta, Jawahar L. ;
Bewtra, Meenakshi ;
Rustgi, Anil ;
Hockstein, Neil ;
Witt, Robert ;
Masters, Gregory ;
Nam, Brian ;
Smirnov, Denis ;
Sepulveda, Manuel A. ;
Gabrilovich, Dmitry I. .
SCIENCE IMMUNOLOGY, 2016, 1 (02)
[6]   Mechanism Regulating Reactive Oxygen Species in Tumor-Induced Myeloid-Derived Suppressor Cells [J].
Corzo, Cesar A. ;
Cotter, Matthew J. ;
Cheng, Pingyan ;
Cheng, Fendong ;
Kusmartsev, Sergei ;
Sotomayor, Eduardo ;
Padhya, Tapan ;
McCaffrey, Thomas V. ;
McCaffrey, Judith C. ;
Gabrilovich, Dmitry I. .
JOURNAL OF IMMUNOLOGY, 2009, 182 (09) :5693-5701
[7]   CXCR2 and CXCR4 antagonistically regulate neutrophil trafficking from murine bone marrow [J].
Eash, Kyle J. ;
Greenbaum, Adam M. ;
Gopalan, Priya K. ;
Link, Daniel C. .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (07) :2423-2431
[8]   Tumor-associated neutrophils stimulate T cell responses in early-stage human lung cancer [J].
Eruslanov, Evgeniy B. ;
Bhojnagarwala, Pratik S. ;
Quatromoni, Jon G. ;
Stephen, Tom Li ;
Ranganathan, Anjana ;
Deshpande, Charuhas ;
Akimova, Tatiana ;
Vachani, Anil ;
Litzky, Leslie ;
Hancock, Wayne W. ;
Conejo-Garcia, Jose R. ;
Feldman, Michael ;
Albeida, Steven M. ;
Singhal, Sunil .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (12) :5466-5480
[9]   MET is required for the recruitment of anti-tumoural neutrophils [J].
Finisguerra, Veronica ;
Di Conza, Giusy ;
Di Matteo, Mario ;
Serneels, Jens ;
Costa, Sandra ;
Thompson, A. A. Roger ;
Wauters, Els ;
Walmsley, Sarah ;
Prenen, Hans ;
Granot, Zvi ;
Casazza, Andrea ;
Mazzone, Massimiliano .
NATURE, 2015, 522 (7556) :349-+
[10]   Polarization of Tumor-Associated Neutrophil Phenotype by TGF-β: "N1" versus "N2" TAN [J].
Fridlender, Zvi G. ;
Sun, Jing ;
Kim, Samuel ;
Kapoor, Veena ;
Cheng, Guanjun ;
Ling, Leona ;
Worthen, G. Scott ;
Albelda, Steven M. .
CANCER CELL, 2009, 16 (03) :183-194