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

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Summary

Introduction

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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