Interferon regulatory factor 1 (IRF-1) and IRF-2 regulate PD-L1 expression in hepatocellular carcinoma (HCC) cells

Cancer Immunol Immunother. 2020 Sep;69(9):1891-1903. doi: 10.1007/s00262-020-02586-9. Epub 2020 May 6.

Abstract

The objective response rate of immune checkpoint blockade (ICB) in hepatocellular carcinoma (HCC) with anti PD-L1/PD-1 therapy is low. Discovering the signaling pathways regulating PD-L1 might help to improve ICB response rates. Here, we investigate transcription factors IRF-1 and IRF-2 signaling pathways regulating PD-L1 in HCC cells. In vivo studies show that IRF-1 and PD-L1 mRNA expression in human HCC tumors are significantly repressed compared with noncancerous background liver. IRF-1, IRF-2, and PD-L1 mRNA expression correlated positively in HCC tumors. Increased IRF-1 mRNA expression was observed in patients with well-differentiated or early stage HCC tumors. In vitro studies show that IFN-γ induces PD-L1 mRNA and protein expression through upregulation of IRF-1 in mouse and human HCC cells. IRF-1, IRF-2, and PD-L1 mRNA expression is upregulated in murine HCC by co-culture with effector T cells from spleen cells incubated with anti-CD3/CD28 antibodies. IRF-2 over-expression down-regulates IFN-γ induced PD-L1 promoter activity and protein levels in a dose-dependent manner. We identify two IRF-1 response elements (IRE1/IRE2) in the upstream 5'-flanking region of the CD274 (PD-L1) gene promoter. Site-directed mutagenesis shows both IRE1 and IRE2 are functional in transfection promoter assays. IRF-1 traditionally functions as tumor suppressor gene. However, these novel findings show a complex role for IRF-1 which upregulates PD-L1 in the inflammatory tumor microenvironment. IRF-1 antagonizes IRF-2 for binding to the IRE promoter element in PD-L1 which gives new insight to the regulation of PD-L1/PD-1 pathways in HCC ICB therapy.

Keywords: HCC; IFN-γ; IRF-1; IRF-2; PD-L1.

MeSH terms

  • Aged
  • Animals
  • B7-H1 Antigen / metabolism*
  • Carcinoma, Hepatocellular / metabolism*
  • Cell Line, Tumor
  • Down-Regulation / physiology
  • Female
  • Hep G2 Cells
  • Humans
  • Interferon Regulatory Factor-1 / metabolism*
  • Interferon Regulatory Factor-2 / metabolism*
  • Interferon-gamma / metabolism
  • Liver Neoplasms / metabolism*
  • Male
  • Mice
  • Signal Transduction / physiology
  • Tumor Microenvironment / physiology
  • Up-Regulation / physiology

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • IRF1 protein, human
  • IRF2 protein, human
  • Interferon Regulatory Factor-1
  • Interferon Regulatory Factor-2
  • Interferon-gamma