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

Authors :
Lee, Jung Hee
Kim, Yong Jun
Ryu, Hyun Woo
Shin, Seung Won
Kim, Eun Ji
Shin, So Hyun
Park, Joon Young
Kim, So Young
Hwang, Chung Su
Na, Joo-Young
Shin, Dong Hoon
Kim, Jee Yeon
Lee, Hyun Jung
Source :
Diagnostic Pathology; 5/16/2023, Vol. 18 Issue 1, p1-7, 7p
Publication Year :
2023

Abstract

Background: Clear cell Renal cell carcinoma (ccRCC) is an immunogenic tumor. B7 family members, such as CTLA-4, PD-1, and PD-L1, are the main components of immune checkpoints that regulate various immune responses. Specifically, B7-H3 regulates T cell-mediated immune responses against cancer. This study aimed to analyze the association between B7-H3 and CTLA-4 expression and the prognostic factors of ccRCC to provide a basis for their potential use as predictive factors and in immunotherapy. Methods: Formalin-fixed paraffin-embedded specimens were obtained from 244 ccRCC patients, and B7-H3, CTLA-4, and PD-L1 expressions were evaluated using immunohistochemical staining. Results: B7-H3 and CTLA-4 were positive in 73 (29.9%) and 57 (23.4%) of the 244 patients, respectively. B7-H3 expression was significantly associated with PD-L1 expression (P < 0.0001); however, CTLA-4 expression was not (P = 0.842). Kaplan–Meier analysis showed that positive B7-H3 expression was associated with poor progression-free survival (PFS) (P < 0.0001), whereas CTLA-4 expression was not (P = 0.457). Multivariate analysis revealed that B7-H3 was correlated with poor PFS (P = 0.031), whereas CTLA-4 was not (P = 0.173). Conclusions: To the best of our knowledge, this study is the first to investigate B7-H3 and PD-L1 expression and survival in ccRCC. B7-H3 expression is an independent prognostic factor for ccRCC. Furthermore, multiple immune cell inhibitory targets, such as B7-H3 and PD-L1, can be used for therapeutic tumor regression in a clinical setting. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17461596
Volume :
18
Issue :
1
Database :
Complementary Index
Journal :
Diagnostic Pathology
Publication Type :
Academic Journal
Accession number :
163739310
Full Text :
https://doi.org/10.1186/s13000-023-01320-0