Neutrophil extracellular traps in cancer: not only catching microbes

被引:0
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作者
Livia Ronchetti
Nouha Setti Boubaker
Maddalena Barba
Patrizia Vici
Aymone Gurtner
Giulia Piaggio
机构
[1] IRCCS - Regina Elena National Cancer Institute,SAFU Unit
[2] The University of Carthage,Laboratory of proteins engineering and bioactive molecules (LIP
[3] IRCCS Regina Elena National Cancer Institute,MB), National Institute of Applied Sciences and Technology of Tunis (INSAT)
[4] Institute of Translational Pharmacology (IFT),Division of Medical Oncology 2
[5] National Research Council (CNR),undefined
关键词
citH3; PAD4; Chemokine receptors; Neutrophils; PD-L1 inhibitors; NET; Cancer liquid biopsies;
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摘要
Neutrophils are the most abundant type of white blood cells circulating throughout the bloodstream and are often considered the frontline defenders in innate immunity. However, neutrophils are increasingly being recognized as having an important role in tumorigenesis and carcinogenesis due to their aberrant activation by molecules released into the tumor microenvironment. One defensive response of neutrophils that is aberrantly triggered during the neoplastic process is called NETosis, where activated neutrophils expel their DNA and intracellular contents in a web-like structure known as a neutrophil extracellular trap (NET). In cancer, NETosis has been linked to increased disease progression, metastasis, and complications such as venous thromboembolism. NET structures released by neutrophils can also serve as a scaffold for clot formation, shining new light on the role of neutrophils and NETosis in coagulation-mediated diseases.
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