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

Front Immunol. 2020 Jul 17:11:1324. doi: 10.3389/fimmu.2020.01324. eCollection 2020.

Abstract

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.

Keywords: CD24; Siglec-10; immune surveillance; immunotherapy; tumor immune escape.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • CD24 Antigen / immunology*
  • Humans
  • Lectins / immunology*
  • Neoplasms / immunology
  • Receptors, Cell Surface / immunology*
  • Tumor Escape*

Substances

  • CD24 Antigen
  • CD24 protein, human
  • Lectins
  • Receptors, Cell Surface
  • SIGLEC10 protein, human