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Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target
In addition to the anti-infection response, neutrophils are linked to tumor progression through the secretion of inflammation components and neutrophil extracellular traps (NETs) formation. NET is a web-like structure constituted by a chromatin scaffold coated with specific nuclear and cytoplasmic p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977644/ https://www.ncbi.nlm.nih.gov/pubmed/36859358 http://dx.doi.org/10.1186/s40364-023-00463-y |
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author | Shang, Bingqing Cui, Honglei Xie, Ruiyang Wu, Jie Shi, Hongzhe Bi, Xingang Feng, Lin Shou, Jianzhong |
author_facet | Shang, Bingqing Cui, Honglei Xie, Ruiyang Wu, Jie Shi, Hongzhe Bi, Xingang Feng, Lin Shou, Jianzhong |
author_sort | Shang, Bingqing |
collection | PubMed |
description | In addition to the anti-infection response, neutrophils are linked to tumor progression through the secretion of inflammation components and neutrophil extracellular traps (NETs) formation. NET is a web-like structure constituted by a chromatin scaffold coated with specific nuclear and cytoplasmic proteins, such as histone and granule peptides. Increasing evidence has demonstrated that NETs are favorable factors to promote tumor growth, invasion, migration, and immunosuppression. However, the cell–cell interaction between NETs and other cells (tumor cells and immune cells) is complicated and poorly studied. This work is the first review to focus on the intercellular communication mediated by NETs in cancer. We summarized the complex cell–cell interaction between NETs and other cells in the tumor microenvironment. We also address the significance of NETs as both prognostic/predictive biomarkers and molecular targets for cancer therapy. Moreover, we presented a comprehensive landscape of cancer immunity, improving the therapeutic efficacy for advanced cancer in the future. |
format | Online Article Text |
id | pubmed-9977644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99776442023-03-02 Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target Shang, Bingqing Cui, Honglei Xie, Ruiyang Wu, Jie Shi, Hongzhe Bi, Xingang Feng, Lin Shou, Jianzhong Biomark Res Review In addition to the anti-infection response, neutrophils are linked to tumor progression through the secretion of inflammation components and neutrophil extracellular traps (NETs) formation. NET is a web-like structure constituted by a chromatin scaffold coated with specific nuclear and cytoplasmic proteins, such as histone and granule peptides. Increasing evidence has demonstrated that NETs are favorable factors to promote tumor growth, invasion, migration, and immunosuppression. However, the cell–cell interaction between NETs and other cells (tumor cells and immune cells) is complicated and poorly studied. This work is the first review to focus on the intercellular communication mediated by NETs in cancer. We summarized the complex cell–cell interaction between NETs and other cells in the tumor microenvironment. We also address the significance of NETs as both prognostic/predictive biomarkers and molecular targets for cancer therapy. Moreover, we presented a comprehensive landscape of cancer immunity, improving the therapeutic efficacy for advanced cancer in the future. BioMed Central 2023-03-02 /pmc/articles/PMC9977644/ /pubmed/36859358 http://dx.doi.org/10.1186/s40364-023-00463-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Shang, Bingqing Cui, Honglei Xie, Ruiyang Wu, Jie Shi, Hongzhe Bi, Xingang Feng, Lin Shou, Jianzhong Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
title | Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
title_full | Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
title_fullStr | Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
title_full_unstemmed | Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
title_short | Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
title_sort | neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9977644/ https://www.ncbi.nlm.nih.gov/pubmed/36859358 http://dx.doi.org/10.1186/s40364-023-00463-y |
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