International journal of radiation oncology, biology, physics | 2018 | Tsang RW, Campbell BA, Goda JS, Kelsey CR
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[Indexed for MEDLINE] 3. Immunity. 2025 Jan 14;58(1):40-58. doi: 10.1016/j.immuni.2024.12.009. Adaptations of neutrophils in cancer. Ng M(1), Cerezo-Wallis D(2), Ng LG(3), Hidalgo A(4). Author information: (1)Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A(∗)STAR), Singapore, Singapore. Electronic address: melissa_ng@immunol.a-star.edu.sg. (2)Vascular Biology and Therapeutics Program and Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA. Electronic address: daniela.cerezo-wallis@yale.edu. (3)Shanghai Immune Therapy Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. Electronic address: nglaiguan@renji.com. (4)Vascular Biology and Therapeutics Program and Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA. Electronic address: andres.hidalgo@yale.edu. There is a renewed interest in neutrophil biology, largely instigated by their prominence in cancer. From an immunologist's perspective, a conceptual breakthrough is the realization that prototypical inflammatory, cytotoxic leukocytes can be tamed to promote the survival and growth of other cells. This has sparked interest in defining the biological principles and molecular mechanisms driving the adaptation of neutrophils to cancer. Yet, many questions remain: is this adaptation mediated by reprogramming mature neutrophils inside the tumoral mass, or rather by rewiring granulopoiesis in the bone marrow? Why, in some instances, are neutrophils beneficial and in others detrimental to cancer? How many different functional programs can be induced in neutrophils by tumors, and is this dependent on the type of tumor? This review summarizes what we know about these questions and discusses therapeutic strategies based on our incipient knowledge of how neutrophils adapt to cancer. Copyright © 2024 Elsevier Inc. All rights reserved. DOI: 10.1016/j.immuni.2024.12.009
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