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Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy

Immune checkpoint molecules, also known as cosignaling molecules, are pivotal cell-surface molecules that control immune cell responses by either promoting (costimulatory molecules) or inhibiting (coinhibitory molecules) a signal. These molecules have been studied for many years. The application of...

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Autores principales: Wu, Baokang, Zhong, Chongli, Lang, Qi, Liang, Zhiyun, Zhang, Yizhou, Zhao, Xin, Yu, Yang, Zhang, Heming, Xu, Feng, Tian, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390200/
https://www.ncbi.nlm.nih.gov/pubmed/34433460
http://dx.doi.org/10.1186/s13046-021-02068-5
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author Wu, Baokang
Zhong, Chongli
Lang, Qi
Liang, Zhiyun
Zhang, Yizhou
Zhao, Xin
Yu, Yang
Zhang, Heming
Xu, Feng
Tian, Yu
author_facet Wu, Baokang
Zhong, Chongli
Lang, Qi
Liang, Zhiyun
Zhang, Yizhou
Zhao, Xin
Yu, Yang
Zhang, Heming
Xu, Feng
Tian, Yu
author_sort Wu, Baokang
collection PubMed
description Immune checkpoint molecules, also known as cosignaling molecules, are pivotal cell-surface molecules that control immune cell responses by either promoting (costimulatory molecules) or inhibiting (coinhibitory molecules) a signal. These molecules have been studied for many years. The application of immune checkpoint drugs in the clinic provides hope for cancer patients. Recently, the poliovirus receptor (PVR)-like protein cosignaling network, which involves several immune checkpoint receptors, i.e., DNAM-1 (DNAX accessory molecule-1, CD226), TIGIT (T-cell immunoglobulin (Ig) and immunoreceptor tyrosine-based inhibitory motif (ITIM)), CD96 (T cell activation, increased late expression (TACLILE)), and CD112R (PVRIG), which interact with their ligands CD155 (PVR/Necl-5), CD112 (PVRL2/nectin-2), CD111 (PVRL1/nectin-1), CD113 (PVRL3/nectin-3), and Nectin4, was discovered. As important components of the immune system, natural killer (NK) and T cells play a vital role in eliminating and killing foreign pathogens and abnormal cells in the body. Recently, increasing evidence has suggested that this novel cosignaling network axis costimulates and coinhibits NK and T cell activation to eliminate cancer cells after engaging with ligands, and this activity may be effectively targeted for cancer immunotherapy. In this article, we review recent advances in research on this novel cosignaling network. We also briefly outline the structure of this cosignaling network, the signaling cascades and mechanisms involved after receptors engage with ligands, and how this novel cosignaling network costimulates and coinhibits NK cell and T cell activation for cancer immunotherapy. Additionally, this review comprehensively summarizes the application of this new network in preclinical trials and clinical trials. This review provides a new immunotherapeutic strategy for cancer treatment.
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spelling pubmed-83902002021-08-27 Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy Wu, Baokang Zhong, Chongli Lang, Qi Liang, Zhiyun Zhang, Yizhou Zhao, Xin Yu, Yang Zhang, Heming Xu, Feng Tian, Yu J Exp Clin Cancer Res Review Immune checkpoint molecules, also known as cosignaling molecules, are pivotal cell-surface molecules that control immune cell responses by either promoting (costimulatory molecules) or inhibiting (coinhibitory molecules) a signal. These molecules have been studied for many years. The application of immune checkpoint drugs in the clinic provides hope for cancer patients. Recently, the poliovirus receptor (PVR)-like protein cosignaling network, which involves several immune checkpoint receptors, i.e., DNAM-1 (DNAX accessory molecule-1, CD226), TIGIT (T-cell immunoglobulin (Ig) and immunoreceptor tyrosine-based inhibitory motif (ITIM)), CD96 (T cell activation, increased late expression (TACLILE)), and CD112R (PVRIG), which interact with their ligands CD155 (PVR/Necl-5), CD112 (PVRL2/nectin-2), CD111 (PVRL1/nectin-1), CD113 (PVRL3/nectin-3), and Nectin4, was discovered. As important components of the immune system, natural killer (NK) and T cells play a vital role in eliminating and killing foreign pathogens and abnormal cells in the body. Recently, increasing evidence has suggested that this novel cosignaling network axis costimulates and coinhibits NK and T cell activation to eliminate cancer cells after engaging with ligands, and this activity may be effectively targeted for cancer immunotherapy. In this article, we review recent advances in research on this novel cosignaling network. We also briefly outline the structure of this cosignaling network, the signaling cascades and mechanisms involved after receptors engage with ligands, and how this novel cosignaling network costimulates and coinhibits NK cell and T cell activation for cancer immunotherapy. Additionally, this review comprehensively summarizes the application of this new network in preclinical trials and clinical trials. This review provides a new immunotherapeutic strategy for cancer treatment. BioMed Central 2021-08-25 /pmc/articles/PMC8390200/ /pubmed/34433460 http://dx.doi.org/10.1186/s13046-021-02068-5 Text en © The Author(s) 2021 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
Wu, Baokang
Zhong, Chongli
Lang, Qi
Liang, Zhiyun
Zhang, Yizhou
Zhao, Xin
Yu, Yang
Zhang, Heming
Xu, Feng
Tian, Yu
Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy
title Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy
title_full Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy
title_fullStr Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy
title_full_unstemmed Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy
title_short Poliovirus receptor (PVR)-like protein cosignaling network: new opportunities for cancer immunotherapy
title_sort poliovirus receptor (pvr)-like protein cosignaling network: new opportunities for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390200/
https://www.ncbi.nlm.nih.gov/pubmed/34433460
http://dx.doi.org/10.1186/s13046-021-02068-5
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