Abstract
Background and objectives: The present study aims to elucidate the clinicopathologic significance of Epstein–Barr virus (EBV) infection in gastric carcinomas (GCs) through a meta-analysis. Materials and Methods: Sixty-one eligible studies were included in the present meta-analysis. The included patients, with and without EBV infection, were 2063 and 17,684, respectively. We investigated the clinicopathologic characteristics and various biomarkers, including programmed death-ligand 1 (PD-L1) expression and tumor-infiltrating lymphocytes (TILs). Results: The estimated EBV-infected rate of GCs was 0.113 (95% confidence interval (CI): 0.088–0.143). The EBV infection rates in GC cells were 0.138 (95% CI: 0.096–0.194), 0.103 (95% CI: 0.077–0.137), 0.080 (95% CI: 0.061–0.106), and 0.042 (95% CI: 0.016–0.106) in the population of Asia, America, Europe, and Africa, respectively. There was a significant difference between EBV-infected and noninfected GCs in the male: female ratio, but not other clinicopathological characteristics. EBV infection rates were higher in GC with lymphoid stroma (0.573, 95% CI: 0.428–0.706) than other histologic types of GCs. There were significant differences in high AT-rich interactive domain-containing protein 1A (ARID1A) and PD-L1 expressions, and high CD8+ TILs between EBV-infected and noninfected GCs. Conclusions: Our results showed that EBV infection of GCs was frequently found in male patients and GCs with lymphoid stroma. EBV infection was significantly correlated with ARID1A and PD-L1 expressions and CD8+ TILs in GCs.
Highlights
The Epstein–Barr virus (EBV) is a ubiquitous human herpesvirus associated with several lymphoid and epithelial malignancies, including Burkitt’s lymphoma, Hodgkin’s lymphoma, nasal NK/T cell lymphoma, and a subset of gastric carcinomas (GCs) [1,2,3,4,5,6]
We investigate the clinicopathologic significance of EBV-associated gastric cancers (EBVaGCs) from eligible studies and perform the subgroup analysis to elucidate the EBV infection rate
We evaluate the differences in the expression of various markers between EBVaGCs and non-EBVaGCs
Summary
The Epstein–Barr virus (EBV) is a ubiquitous human herpesvirus associated with several lymphoid and epithelial malignancies, including Burkitt’s lymphoma, Hodgkin’s lymphoma, nasal NK/T cell lymphoma, and a subset of gastric carcinomas (GCs) [1,2,3,4,5,6]. In 1990, Burke et al first detected the EBV genomes in a small group of GCs using a polymerase chain reaction [1]. EBV genomes were uniformly present in GC cells, resembling lymphoepithelioma cells [4]. EBV involvement was detected in lymphoepithelioma-like GCs and in a subset of ordinary GCs [4,7]. The present study aims to elucidate the clinicopathologic significance of Epstein–Barr virus (EBV) infection in gastric carcinomas (GCs) through a meta-analysis
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