Neutrophil phenotypes and functions in cancer: A consensus statement Review


Authors: Quail, D. F.; Amulic, B.; Aziz, M.; Barnes, B. J.; Eruslanov, E.; Fridlender, Z. G.; Goodridge, H. S.; Granot, Z.; Hidalgo, A.; Huttenlocher, A.; Kaplan, M. J.; Malanchi, I.; Merghoub, T.; Meylan, E.; Mittal, V.; Pittet, M. J.; Rubio-Ponce, A.; Udalova, I. A.; van den Berg, T. K.; Wagner, D. D.; Wang, P.; Zychlinsky, A.; de Visser, K. E.; Egeblad, M.; Kubes, P.
Review Title: Neutrophil phenotypes and functions in cancer: A consensus statement
Abstract: There is a growing appreciation for the vastness of neutrophil functional states in cancer. Quail et al. provide a consensus statement on mechanisms governing neutrophil heterogeneity in the context of malignancy and discuss controversies and solutions in neutrophil research. Neutrophils are the first responders to infection and inflammation and are thus a critical component of innate immune defense. Understanding the behavior of neutrophils as they act within various inflammatory contexts has provided insights into their role in sterile and infectious diseases; however, the field of neutrophils in cancer is comparatively young. Here, we summarize key concepts and current knowledge gaps related to the diverse roles of neutrophils throughout cancer progression. We discuss sources of neutrophil heterogeneity in cancer and provide recommendations on nomenclature for neutrophil states that are distinct in maturation and activation. We address discrepancies in the literature that highlight a need for technical standards that ought to be considered between laboratories. Finally, we review emerging questions in neutrophil biology and innate immunity in cancer. Overall, we emphasize that neutrophils are a more diverse population than previously appreciated and that their role in cancer may present novel unexplored opportunities to treat cancer.
Keywords: neutrophils; growth-factor-beta; colony-stimulating factor; hematopoietic stem-cells; suppressor-cells; deep-vein thrombosis; low-density; peptidylarginine deiminase 4; reduced clinical benefit; extracellular trap formation; tumor-associated neutrophils
Journal Title: Journal of Experimental Medicine
Volume: 219
Issue: 6
ISSN: 0022-1007
Publisher: Rockefeller University Press  
Date Published: 2022-06-06
Start Page: e20220011
Language: English
ACCESSION: WOS:000893108300001
DOI: 10.1084/jem.20220011
PROVIDER: wos
PMCID: PMC9086501
PUBMED: 35522219
Notes: Review -- e20220011 -- Source: Wos
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  1. Taha Merghoub
    364 Merghoub