Linking cell-surface GRP78 to cancer: From basic research to clinical value of GRP78 antibodies

Cancer Lett. 2022 Jan 1:524:1-14. doi: 10.1016/j.canlet.2021.10.004. Epub 2021 Oct 9.

Abstract

Glucose-related protein 78 (GRP78) is a chaperone protein localized primarily in the endoplasmic reticulum (ER) lumen, where it helps in proper protein folding by targeting misfolded proteins and facilitating protein assembly. In stressed cells, GRP78 is translocated to the cell surface (csGRP78) where it binds to various ligands and triggers different intracellular pathways. Thus, csGRP78 expression is associated with cancer, involved in the maintenance and progression of the disease. Extracellular exposition of csGRP78 leads to the production of autoantibodies as observed in patients with prostate or ovarian cancer, in which the ability to target csGRP78 affects the tumor development. Present on the surface of cancer cells and not normal cells in vivo, csGRP78 represents an interesting target for therapeutic antibody strategies. Here we give an overview of the csGRP78 function in the cell and its role in oncogenesis, thereby providing insight into the clinical value of GRP78 monoclonal antibodies for cancer prognosis and treatment.

Keywords: Cell-surface GRP78; GRP78 antibodies; Prognosis; Therapy; Tumor development.

Publication types

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

MeSH terms

  • Autoantibodies / immunology
  • Endoplasmic Reticulum / genetics
  • Endoplasmic Reticulum / immunology
  • Endoplasmic Reticulum Chaperone BiP / genetics*
  • Endoplasmic Reticulum Chaperone BiP / immunology
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / immunology
  • Ovarian Neoplasms / genetics*
  • Ovarian Neoplasms / immunology
  • Ovarian Neoplasms / pathology
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / immunology
  • Prostatic Neoplasms / pathology
  • Signal Transduction

Substances

  • Autoantibodies
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Membrane Proteins