M2 macrophages promote PD-L1 expression in triple-negative breast cancer via secreting CXCL1

Pathol Res Pract. 2024 Aug:260:155458. doi: 10.1016/j.prp.2024.155458. Epub 2024 Jul 9.

Abstract

Background: M2 macrophages are known to play a significant role in the progression of triple-negative breast cancer (TNBC) by creating an immunosuppressive microenvironment. The aim of this study is to investigate the impact of M2 macrophages on TNBC and their correlation with programmed death-ligand 1 (PD-L1) expression.

Methods: We employed a co-culture system to analyze the role of the mutual regulation of M2 macrophages and TNBC cells. Employing a multifaceted approach, including bioinformatics analysis, Western blotting, flow cytometry analysis, ELISA, qRT-PCR, lentivirus infection, mouse models, and IHC, we aimed to elucidate the influence and mechanism of M2 macrophages on PD-L1 expression.

Results: The results showed a substantial infiltration of M2 macrophages in TNBC tissue, which demonstrated a positive correlation with PD-L1 expression. CXCL1 exhibited abnormally high expression in M2 macrophages and enhanced the expression of PD-L1 in TNBC cells. Notably, silencing CXCL1 or its receptor CXCR2 inhibited M2 macrophages-induced expression of PD-L1. Mechanistically, CXCL1 derived from M2 macrophages binding to CXCR2 activated the PI3K/AKT/NF-κB signaling pathway, resulting in increased PD-L1 expression in TNBC.

Conclusion: Broadly speaking, these results provide evidence for the immunosuppressive role of M2 macrophages and CXCL1 in TNBC cells, indicating their potential as therapeutic biomarkers.

Keywords: C-X-C motif chemokine ligand 1; Oncoimmunology; Programmed death-ligand 1; Triple-negative breast cancer; Tumor-associated macrophages.

MeSH terms

  • Animals
  • B7-H1 Antigen* / metabolism
  • Cell Line, Tumor
  • Chemokine CXCL1* / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Macrophages* / immunology
  • Macrophages* / metabolism
  • Mice
  • Signal Transduction
  • Triple Negative Breast Neoplasms* / immunology
  • Triple Negative Breast Neoplasms* / metabolism
  • Triple Negative Breast Neoplasms* / pathology
  • Tumor Microenvironment / immunology

Substances

  • B7-H1 Antigen
  • Chemokine CXCL1
  • CD274 protein, human
  • CXCL1 protein, human