4.6 Article

Prognostic value of hypoxia-inducible factor-1 alpha and prolyl 4-hydroxylase beta polypeptide overexpression in gastric cancer

Journal

WORLD JOURNAL OF GASTROENTEROLOGY
Volume 24, Issue 22, Pages 2381-2391

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.3748/wjg.v24.i22.2381

Keywords

Gastric cancer; Hypoxia inducible factor-1 alpha; Prolyl 4-hydroxylase beta polypeptide; Overall survival; Clinicopathological predictors; Disease free survival

Funding

  1. Liaoning S and T Project [2015020269]
  2. Liaoning Province Cancer Hospital and Institute [Z1410]

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AIM To investigate the relationship between hypoxia-inducible factor-1 alpha (HIF-1 alpha), prolyl 4-hydroxylase beta (P4HB) expression, and clinicopathologic parameters, as well as the prognostic value of these genes for patients with gastric cancer (GC). METHODS Hypoxia is a critical factor that shapes the GC micro-environment. In previous reports, we have demonstrated that P4HB is a potential target of HIF-1 alpha. In the present study, gene expression profiling interactive analysis (GEPIA) was used to analyze the relationship between P4HB and hypoxia-associated genes. To this end, 428 GC tissue samples were used to analyze the expression of HIF-1 alpha and P4HB via immunohistochemical staining. Patient samples were classified as having weak-expression or over-expression both in terms of HIF-1 alpha and P4HB. Correlations between biomarkers and clinicopathological factors were analyzed to predict survival. RESULTS P4HB demonstrated a positive correlation with hypoxia-associated genes (P < 0.05). HIF-1 alpha and P4HB overexpression have a significant correlation with TNM staging (chi(2) = 23.32, P = 0.00; chi(2) = 65.64, P = 0.00) and peritoneum cavity metastasis (chi(2) = 12.67, P = 0.00; chi(2) = 39.29, P = 0.00). In univariate analysis, patients with a high HIF-1 alpha expression trend had a shorter disease-free survival (DFS: 44.80 mo vs 22.06 mo) and overall survival (OS: 49.58 mo vs 39.92 mo). P4HB overexpression reflected similar results: patients with over-expression of P4HB had a shorter survival time than those with weak-expression (DFS: 48.03 mo vs 29.64 mo, OS: 52.48 mo vs 36.87 mo). Furthermore, HIF-1 alpha is also a clinicopathological predictor of dismal prognosis according to multivariate analysis (DFS, 95% CI: 0.52-0.88, P < 0.00; OS, 95% CI: 0.50-0.85, P < 0.00). However, P4HB was meaningful in DFS (95% CI: 0.58-1.00, P < 0.05) but not in OS (95% CI: 0.72-1.23, P > 0.05). CONCLUSION Overexpression of HIF-1 alpha and P4HB is associated with poor prognosis in patients with GC. Thus, these genes may be potential prognostic biomarker candidates in GC.

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