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CD155, an onco‐immunologic molecule in human tumors

CD155 is the fifth member in the nectin‐like molecule family, and functions as the receptor of poliovirus; therefore, CD155 is also referred to as necl‐5, or PVR. As an immunoglobulin‐like adhesion molecule, CD155 is involved in cell motility, and natural killer and T cell‐mediated immunity. CD155 i...

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Detalles Bibliográficos
Autores principales: Gao, Jian, Zheng, Qianqian, Xin, Na, Wang, Wei, Zhao, Chenghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623745/
https://www.ncbi.nlm.nih.gov/pubmed/28730595
http://dx.doi.org/10.1111/cas.13324
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author Gao, Jian
Zheng, Qianqian
Xin, Na
Wang, Wei
Zhao, Chenghai
author_facet Gao, Jian
Zheng, Qianqian
Xin, Na
Wang, Wei
Zhao, Chenghai
author_sort Gao, Jian
collection PubMed
description CD155 is the fifth member in the nectin‐like molecule family, and functions as the receptor of poliovirus; therefore, CD155 is also referred to as necl‐5, or PVR. As an immunoglobulin‐like adhesion molecule, CD155 is involved in cell motility, and natural killer and T cell‐mediated immunity. CD155 is barely or weakly expressed in various normal human tissues, but frequently overexpressed in human malignant tumors. CD155 overexpression promotes tumor cell invasion and migration, and is associated with tumor progression and poor prognosis. As the ligand for both costimulatory receptor CD226 and coinhibitory receptor TIGIT and CD96 on natural killer and T cells, CD155 seems to play a dual role in oncoimmunity. However, some recent studies indicate that CD155 overexpression may induce tumor immune escape. Taken together, CD155 may be considered as a target for the treatment of tumors with CD155 overexpression.
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spelling pubmed-56237452017-10-04 CD155, an onco‐immunologic molecule in human tumors Gao, Jian Zheng, Qianqian Xin, Na Wang, Wei Zhao, Chenghai Cancer Sci Review Articles CD155 is the fifth member in the nectin‐like molecule family, and functions as the receptor of poliovirus; therefore, CD155 is also referred to as necl‐5, or PVR. As an immunoglobulin‐like adhesion molecule, CD155 is involved in cell motility, and natural killer and T cell‐mediated immunity. CD155 is barely or weakly expressed in various normal human tissues, but frequently overexpressed in human malignant tumors. CD155 overexpression promotes tumor cell invasion and migration, and is associated with tumor progression and poor prognosis. As the ligand for both costimulatory receptor CD226 and coinhibitory receptor TIGIT and CD96 on natural killer and T cells, CD155 seems to play a dual role in oncoimmunity. However, some recent studies indicate that CD155 overexpression may induce tumor immune escape. Taken together, CD155 may be considered as a target for the treatment of tumors with CD155 overexpression. John Wiley and Sons Inc. 2017-08-18 2017-10 /pmc/articles/PMC5623745/ /pubmed/28730595 http://dx.doi.org/10.1111/cas.13324 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Gao, Jian
Zheng, Qianqian
Xin, Na
Wang, Wei
Zhao, Chenghai
CD155, an onco‐immunologic molecule in human tumors
title CD155, an onco‐immunologic molecule in human tumors
title_full CD155, an onco‐immunologic molecule in human tumors
title_fullStr CD155, an onco‐immunologic molecule in human tumors
title_full_unstemmed CD155, an onco‐immunologic molecule in human tumors
title_short CD155, an onco‐immunologic molecule in human tumors
title_sort cd155, an onco‐immunologic molecule in human tumors
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623745/
https://www.ncbi.nlm.nih.gov/pubmed/28730595
http://dx.doi.org/10.1111/cas.13324
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