Prognostic Significance of High EphA1-4 Expression Levels in Locally Advanced Gastric Cancer

Anticancer Res. 2018 Mar;38(3):1685-1693. doi: 10.21873/anticanres.12402.

Abstract

Background/aim: Erythropoietin-producing hepatocellular carcinoma receptor A (EphA) is associated with angiogenesis and invasive tumor progression. In this study, we evaluated the EphA1-4 expression levels in advanced gastric cancer.

Patients and methods: Tumor tissues obtained from 114 patients with advanced gastric adenocarcinoma who underwent gastrectomy were analyzed. In addition, the impact of EPHA 1-4 mRNA expression on survival was analyzed using the Kaplan-Meier plotter database on the website.

Results: High EphA 1, 2, and 4 expression levels were significantly related to recurrence (p<0.01, p=0.04, and p<0.01). Both high EphA 1 and 4 expression levels were independent predictors of relapse-free interval (hazard ratio [HR]=2.0, p=0.03; HR=2.4, p=0.03) and disease-specific survival (HR=2.0, 95% p=0.03; HR=2.5, p=0.02) on multivariate analysis. In the Kaplan-Meier plotter database, high EPHA2 mRNA expression was significantly associated with poor survival in patients with gastric cancer (p=0.0098), and high expression levels of EPHA1 and 4 tended to be associated with poor survival (p=0.050, p=0.052).

Conclusion: EphA 1, 2, and 4 may play key roles in recurrence and survival in patients with advanced gastric cancer.

Keywords: Erythropoietin-producing hepatocellular carcinoma receptors; advanced gastric cancer.

MeSH terms

  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Adenocarcinoma / surgery
  • Aged
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Neoplasm Recurrence, Local
  • Outcome Assessment, Health Care / methods
  • Outcome Assessment, Health Care / statistics & numerical data
  • Prognosis
  • Proportional Hazards Models
  • Receptor, EphA1 / genetics*
  • Receptor, EphA1 / metabolism
  • Receptor, EphA2 / genetics*
  • Receptor, EphA2 / metabolism
  • Receptor, EphA3 / genetics*
  • Receptor, EphA3 / metabolism
  • Receptor, EphA4 / genetics*
  • Receptor, EphA4 / metabolism
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology
  • Stomach Neoplasms / surgery

Substances

  • Receptor, EphA1
  • Receptor, EphA2
  • Receptor, EphA3
  • Receptor, EphA4