Sialylated glycoproteins suppress immune cell killing by binding to Siglec-7 and Siglec-9 in prostate cancer

J Clin Invest. 2024 Oct 22;134(24):e180282. doi: 10.1172/JCI180282.

Abstract

Prostate cancer is the second leading cause of male cancer death in the U.S. Current immune checkpoint inhibitor-based immunotherapies have improved survival for many malignancies; however, they have failed to prolong survival for prostate cancer. Siglecs (sialic acid-binding immunoglobulin-like lectins) are expressed on immune cells and regulate their function. Siglec-7 and Siglec-9 contribute to immune evasion in cancer by interacting with sialic acid-containing glycoprotein ligands on cancer cells. However, the role of Siglec-7/9 receptors and their ligands in prostate cancer remains poorly understood. Here, we find that Siglec-7 and Siglec-9 are associated with poor prognosis in patients with prostate cancer and are highly expressed in myeloid cells, including macrophages, in prostate tumor tissues. Siglec-7 and -9 ligands were expressed in prostate cancer cells and human prostate tumor tissues. Blocking the interactions between Siglec-7/9 and sialic acids inhibited prostate cancer xenograft growth and increased immune cell infiltration in humanized mice in vivo. Using a CRISPRi screen and mass spectrometry, we identified CD59 as a candidate Siglec-9 ligand in prostate cancer. The identification of Siglec-7 and -9 as potential therapeutic targets, including the CD59/Siglec-9 axis, opens up opportunities for immune-based interventions in prostate cancer.

Keywords: Cancer immunotherapy; Immunotherapy; Oncology; Prostate cancer.

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • Antigens, Differentiation, B-Lymphocyte / genetics
  • Antigens, Differentiation, B-Lymphocyte / immunology
  • Antigens, Differentiation, B-Lymphocyte / metabolism
  • Antigens, Differentiation, Myelomonocytic / genetics
  • Antigens, Differentiation, Myelomonocytic / immunology
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Cell Line, Tumor
  • Glycoproteins / genetics
  • Glycoproteins / immunology
  • Glycoproteins / metabolism
  • Humans
  • Lectins* / genetics
  • Lectins* / immunology
  • Lectins* / metabolism
  • Male
  • Mice
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / immunology
  • Neoplasm Proteins / metabolism
  • Prostatic Neoplasms* / genetics
  • Prostatic Neoplasms* / immunology
  • Prostatic Neoplasms* / metabolism
  • Prostatic Neoplasms* / pathology
  • Sialic Acid Binding Immunoglobulin-like Lectins / genetics
  • Sialic Acid Binding Immunoglobulin-like Lectins / immunology
  • Sialic Acid Binding Immunoglobulin-like Lectins / metabolism

Substances

  • SIGLEC9 protein, human
  • SIGLEC7 protein, human
  • Lectins
  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Antigens, Differentiation, B-Lymphocyte
  • Glycoproteins
  • Sialic Acid Binding Immunoglobulin-like Lectins
  • Neoplasm Proteins