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Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment

Nasopharyngeal carcinoma (NPC) arises from the epithelial cells located in the nasopharynx and has a distinct geographic distribution. Chronic Epstein-Barr virus (EBV) infection, as its most common causative agents, can be detected in 100% of NPC types. In-depth studies of the cellular and molecular...

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Autores principales: Jiang, Jianyun, Ying, Hongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375932/
https://www.ncbi.nlm.nih.gov/pubmed/35964134
http://dx.doi.org/10.1186/s13046-022-02457-4
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author Jiang, Jianyun
Ying, Hongmei
author_facet Jiang, Jianyun
Ying, Hongmei
author_sort Jiang, Jianyun
collection PubMed
description Nasopharyngeal carcinoma (NPC) arises from the epithelial cells located in the nasopharynx and has a distinct geographic distribution. Chronic Epstein-Barr virus (EBV) infection, as its most common causative agents, can be detected in 100% of NPC types. In-depth studies of the cellular and molecular events leading to immunosuppression in NPC have revealed new therapeutic targets and diverse combinations that promise to benefit patients with highly refractory, advanced and metastatic NPC. This paper reviews the mechanisms by which NPC cells to circumvent immune surveillance and approaches being attempted to restore immunity. We integrate existing insights into anti-NPC immunity and molecular signaling pathways as well as targeting therapies in anticipation of broader applicability and effectiveness in advanced metastatic NPC.
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spelling pubmed-93759322022-08-15 Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment Jiang, Jianyun Ying, Hongmei J Exp Clin Cancer Res Review Nasopharyngeal carcinoma (NPC) arises from the epithelial cells located in the nasopharynx and has a distinct geographic distribution. Chronic Epstein-Barr virus (EBV) infection, as its most common causative agents, can be detected in 100% of NPC types. In-depth studies of the cellular and molecular events leading to immunosuppression in NPC have revealed new therapeutic targets and diverse combinations that promise to benefit patients with highly refractory, advanced and metastatic NPC. This paper reviews the mechanisms by which NPC cells to circumvent immune surveillance and approaches being attempted to restore immunity. We integrate existing insights into anti-NPC immunity and molecular signaling pathways as well as targeting therapies in anticipation of broader applicability and effectiveness in advanced metastatic NPC. BioMed Central 2022-08-13 /pmc/articles/PMC9375932/ /pubmed/35964134 http://dx.doi.org/10.1186/s13046-022-02457-4 Text en © The Author(s) 2022 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
Jiang, Jianyun
Ying, Hongmei
Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
title Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
title_full Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
title_fullStr Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
title_full_unstemmed Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
title_short Revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
title_sort revealing the crosstalk between nasopharyngeal carcinoma and immune cells in the tumor microenvironment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375932/
https://www.ncbi.nlm.nih.gov/pubmed/35964134
http://dx.doi.org/10.1186/s13046-022-02457-4
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