B7-H3 expression is associated with high PD-L1 expression in clear cell renal cell carcinoma and predicts poor

Jung Hee Lee1, Yong Jun Kim2, Hyun Woo Ryu2

  • 1Department of Pathology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Korea.

Diagnostic Pathology
|March 9, 2023
PubMed
Abstract

Insights

B7-H3 expression is a significant prognostic factor in clear cell renal cell carcinoma (ccRCC), correlating with poorer progression-free survival. This finding suggests B7-H3, alongside PD-L1, may serve as a therapeutic target for ccRCC immunotherapy.

Area of Science:

  • Oncology
  • Immunology
  • Cancer Research

Background:

  • Clear cell renal cell carcinoma (ccRCC) is an immunogenic malignancy.
  • Immune checkpoints, including B7 family members like B7-H3, CTLA-4, PD-1, and PD-L1, regulate anti-tumor immune responses.
  • B7-H3 plays a role in T cell-mediated immunity against cancer.

Purpose of the Study:

  • To investigate the association between B7-H3 and CTLA-4 expression and prognostic factors in ccRCC.
  • To evaluate the potential of B7-H3 and CTLA-4 as predictive biomarkers for ccRCC.
  • To explore their relevance in the context of cancer immunotherapy.

Main Methods:

  • Immunohistochemical staining was performed on 244 ccRCC patient specimens.
  • Expression levels of B7-H3, CTLA-4, and PD-L1 were assessed.
  • Statistical analyses, including Kaplan-Meier and multivariate analyses, were conducted to evaluate survival outcomes.

Main Results:

  • B7-H3 expression was detected in 29.9% of patients, and CTLA-4 in 23.4%.
  • Positive B7-H3 expression was significantly associated with PD-L1 expression and poorer progression-free survival (PFS).
  • CTLA-4 expression showed no significant association with PD-L1 expression or PFS.

Conclusions:

  • B7-H3 expression is an independent prognostic factor for ccRCC, indicating poorer PFS.
  • This study is the first to link B7-H3 and PD-L1 expression with survival in ccRCC.
  • Targeting multiple immune inhibitory molecules, such as B7-H3 and PD-L1, may enhance therapeutic tumor regression in ccRCC.