Inhibition of programmed death ligand 1 (PD-L1) expression in breast cancer cells by sesamin

Int Immunopharmacol. 2020 Sep:86:106759. doi: 10.1016/j.intimp.2020.106759. Epub 2020 Jul 11.

Abstract

Programmed death ligand 1 (PD-L1) is overexpressed in some metastatic breast cancer subtypes, specifically triple-negative breast cancer (TNBC). This feature can assist in the eradication of anti-tumor immunity, thereby enhancing the survival of the tumor. This study aims to explore how sesamin affects PD-L1 expression in breast cancer cells and its related molecular mechanisms. We found high levels of expression of PD-L1 in both mRNA and protein levels in the TNBC cell line, MDA-MB231, but not in the luminal type-breast cancer cell line, MCF-7. We then demonstrated the tumor suppressive effect of sesamin, which induced the inhibition of cell proliferation in MDA-MB231 cells. Additionally, sesamin triggered PD-L1 downregulation (both mRNA and protein) through the inhibition of AKT, NF-κB and JAK/Stat signaling in MDA-MB231 cells. Moreover, the migration ability of MDA-MB231 cells was effectively diminished by sesamin via inhibition of the activation of MMP-9 and MMP-2. In summary, this study demonstrated that sesamin suppresses MDA-MB231 breast cancer cells' proliferation and migration; and decreases the expression of PD-L1 via the downregulation of AKT, NF-κB, and JAK/Stat signaling. Therefore, sesamin may be an effective alternative and novel therapeutic option for immunotherapy in breast cancer cells with high PD-L1 expression.

Keywords: Breast cancer; Immunotherapy; NF-κB; Programmed death ligand 1; Sesamin.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • B7-H1 Antigen / genetics
  • B7-H1 Antigen / metabolism*
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / drug therapy*
  • Cell Proliferation
  • Dioxoles / pharmacology*
  • Female
  • Humans
  • Janus Kinases / metabolism
  • Lignans / pharmacology*
  • MCF-7 Cells
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • NF-kappa B / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • STAT Transcription Factors / metabolism
  • Signal Transduction
  • Triple Negative Breast Neoplasms / drug therapy*
  • Up-Regulation

Substances

  • B7-H1 Antigen
  • Biomarkers, Tumor
  • CD274 protein, human
  • Dioxoles
  • Lignans
  • NF-kappa B
  • STAT Transcription Factors
  • Janus Kinases
  • Proto-Oncogene Proteins c-akt
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9
  • sesamin