The Mincle/Syk/NF-κB Signaling Circuit Is Essential for Maintaining the Protumoral Activities of Tumor-Associated Macrophages

Cancer Immunol Res. 2020 Aug;8(8):1004-1017. doi: 10.1158/2326-6066.CIR-19-0782. Epub 2020 Jun 12.

Abstract

Tumor-associated macrophages (TAM) have important roles in cancer progression, but the signaling behind the formation of protumoral TAM remains understudied. Here, by single-cell RNA sequencing, we revealed that the pattern recognition receptor Mincle was highly expressed in TAM and significantly associated with mortality in patients with non-small cell lung cancer. Cancer cells markedly induced Mincle expression in bone marrow-derived macrophages (BMDM), thus promoting cancer progression in invasive lung carcinoma LLC and melanoma B16F10 in vivo and in vitro Mincle was predominately expressed in the M2-like TAM in non-small cell lung carcinoma and LLC tumors, and silencing of Mincle unexpectedly promoted M1-like phenotypes in vitro Mechanistically, we discovered a novel Mincle/Syk/NF-κB signaling pathway in TAM needed for executing their TLR4-independent protumoral activities. Adoptive transfer of Mincle-silenced BMDM significantly suppressed TAM-driven cancer progression in the LLC-bearing NOD/SCID mice. By modifying our well-established ultrasound microbubble-mediated gene transfer protocol, we demonstrated that tumor-specific silencing of Mincle effectively blocked Mincle/Syk/NF-κB signaling, therefore inhibiting the TAM-driven cancer progression in the syngeneic mouse cancer models. Thus, our findings highlight the function of Mincle as a novel immunotherapeutic target for cancer via blocking the Mincle/Syk/NF-κB circuit in TAM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Cell Line, Tumor
  • Cytokines / immunology
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Humans
  • Lectins, C-Type / immunology
  • Lectins, C-Type / metabolism*
  • Lung Neoplasms / immunology*
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Macrophages / immunology
  • Macrophages / pathology
  • Male
  • Melanoma / immunology*
  • Melanoma / metabolism
  • Melanoma / pathology
  • Membrane Proteins / immunology
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Mice, SCID
  • Middle Aged
  • NF-kappa B / immunology
  • NF-kappa B / metabolism*
  • Receptors, Immunologic / immunology
  • Receptors, Immunologic / metabolism*
  • Signal Transduction
  • Syk Kinase / immunology
  • Syk Kinase / metabolism*
  • Tumor-Associated Macrophages / immunology*
  • Tumor-Associated Macrophages / pathology

Substances

  • CLEC4D protein, human
  • Clecsf8 protein, mouse
  • Cytokines
  • Lectins, C-Type
  • Membrane Proteins
  • NF-kappa B
  • Receptors, Immunologic
  • Syk Kinase