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Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10

Tumor immune escape is an important part of tumorigenesis and development. Tumor cells can develop a variety of immunosuppressive mechanisms to combat tumor immunity. Exploring tumor cells that escape immune surveillance through the molecular mechanism of related immunosuppression in-depth is helpfu...

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Detalles Bibliográficos
Autores principales: Yin, Shan-Shan, Gao, Feng-Hou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379889/
https://www.ncbi.nlm.nih.gov/pubmed/32765491
http://dx.doi.org/10.3389/fimmu.2020.01324
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author Yin, Shan-Shan
Gao, Feng-Hou
author_facet Yin, Shan-Shan
Gao, Feng-Hou
author_sort Yin, Shan-Shan
collection PubMed
description Tumor immune escape is an important part of tumorigenesis and development. Tumor cells can develop a variety of immunosuppressive mechanisms to combat tumor immunity. Exploring tumor cells that escape immune surveillance through the molecular mechanism of related immunosuppression in-depth is helpful to develop the treatment strategies of targeted tumor immune escape. The latest studies show that CD24 on the surface of tumor cells interacts with Siglec-10 on the surface of immune cells to promote the immune escape of tumor cells. It is necessary to comment on the molecular mechanism of inhibiting the activation of immune cells through the interaction between CD24 on tumor cells and Siglec-10 on immune cells, and a treatment strategy of tumors through targeting CD24 on the surface of tumor cells or Siglec-10 on immune cells.
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spelling pubmed-73798892020-08-05 Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10 Yin, Shan-Shan Gao, Feng-Hou Front Immunol Immunology Tumor immune escape is an important part of tumorigenesis and development. Tumor cells can develop a variety of immunosuppressive mechanisms to combat tumor immunity. Exploring tumor cells that escape immune surveillance through the molecular mechanism of related immunosuppression in-depth is helpful to develop the treatment strategies of targeted tumor immune escape. The latest studies show that CD24 on the surface of tumor cells interacts with Siglec-10 on the surface of immune cells to promote the immune escape of tumor cells. It is necessary to comment on the molecular mechanism of inhibiting the activation of immune cells through the interaction between CD24 on tumor cells and Siglec-10 on immune cells, and a treatment strategy of tumors through targeting CD24 on the surface of tumor cells or Siglec-10 on immune cells. Frontiers Media S.A. 2020-07-17 /pmc/articles/PMC7379889/ /pubmed/32765491 http://dx.doi.org/10.3389/fimmu.2020.01324 Text en Copyright © 2020 Yin and Gao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Yin, Shan-Shan
Gao, Feng-Hou
Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10
title Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10
title_full Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10
title_fullStr Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10
title_full_unstemmed Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10
title_short Molecular Mechanism of Tumor Cell Immune Escape Mediated by CD24/Siglec-10
title_sort molecular mechanism of tumor cell immune escape mediated by cd24/siglec-10
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379889/
https://www.ncbi.nlm.nih.gov/pubmed/32765491
http://dx.doi.org/10.3389/fimmu.2020.01324
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