Expression and relationship of PD-L1, CD24, and CD47 in hepatitis B virus associated hepatocellular carcinoma

Sci Rep. 2024 Dec 28;14(1):31530. doi: 10.1038/s41598-024-83145-5.

Abstract

Immune checkpoint inhibitor (ICI) therapy is the new standard treatment for advanced or metastatic hepatocellular carcinoma (HCC); however, many patients still fail to respond. This study explored the expression and prognosis of programmed death ligand 1 (PD-L1), cluster of differentiation 24 (CD24), and cluster of differentiation 47 (CD47) in patients with hepatitis B virus-associated HCC (HBV-associated HCC). We analyzed sequencing data from the Cancer Genome Atlas (TCGA) and investigated the expression of PD-L1, CD24, and CD47 in HBV-associated HCC patients by immunohistochemistry and their relationship with prognosis and clinicopathological factors. HCC data from the TCGA database show that PD-L1 was substantially correlated with various immune cells. In 67 patients with HBV-associated HCC, high PD-L1 and CD24 expression levels were related to poor overall survival (OS) and progression-free survival (PFS). PD-L1 expression was significantly associated with the staging of HBV-associated HCC (p = 0.011) and Ki67 expression (p = 0.024). Correlation analysis between variables reveals that PD-L1 was significantly positively correlated with CD24 and CD47. High expression of PD-L1 and CD24 are risk factors for poor prognosis in HBV-associated HCC patients following curative resection. PD-L1 is significantly correlated with CD24 and CD47.

Keywords: CD24; CD47; HBV-associated hepatocellular carcinoma; Immune checkpoint inhibitors; PD-L1.

MeSH terms

  • Adult
  • Aged
  • B7-H1 Antigen* / genetics
  • B7-H1 Antigen* / metabolism
  • Biomarkers, Tumor / metabolism
  • CD24 Antigen* / genetics
  • CD24 Antigen* / metabolism
  • CD47 Antigen* / genetics
  • CD47 Antigen* / metabolism
  • Carcinoma, Hepatocellular* / genetics
  • Carcinoma, Hepatocellular* / metabolism
  • Carcinoma, Hepatocellular* / mortality
  • Carcinoma, Hepatocellular* / pathology
  • Carcinoma, Hepatocellular* / virology
  • Female
  • Gene Expression Regulation, Neoplastic
  • Hepatitis B / complications
  • Hepatitis B / metabolism
  • Hepatitis B / virology
  • Hepatitis B virus* / genetics
  • Humans
  • Liver Neoplasms* / genetics
  • Liver Neoplasms* / metabolism
  • Liver Neoplasms* / pathology
  • Liver Neoplasms* / virology
  • Male
  • Middle Aged
  • Prognosis

Substances

  • CD24 Antigen
  • B7-H1 Antigen
  • CD274 protein, human
  • CD47 Antigen
  • CD24 protein, human
  • CD47 protein, human
  • Biomarkers, Tumor