The expression of the hypoxia markers CA9 and CXCR4 is correlated with survival in patients with neuroendocrine tumours of the ileum

Neuroendocrinology. 2012;95(3):214-22. doi: 10.1159/000329873. Epub 2011 Nov 29.

Abstract

Background/aim: The hypoxia-inducible factor pathway regulates the expression of a diverse group of molecules such as CA9 and CXCR4. Our aim was to investigate the expression of these markers in a series of patients with an ileal neuroendocrine tumour (IET) at various stages of tumorigenesis.

Methods: The immunohistochemical expression of CA9 and CXCR4 was examined in 51 patients with a resected IET. A 'hypoxic score' was calculated, integrating the expression of both CA9 and CXCR4 (hypoxic score 0: absence of expression of both molecules; hypoxic score 1: expression of CXCR4 and/or CA9). Results were compared to histoprognostic factors (including tumour size, stage and grade, WHO and TNM classifications, presence of vascular or perineural invasion, presence of a fibrotic stroma and microvascular density) and to survival.

Results: All tumours were well differentiated. 69% of tumours were less than 25 mm. 46% of tumours largely infiltrated the intestinal wall (≥T3, subserosa and serosa) and 90% were classified as N1 and/or 63% as M1. 57% of tumours were of grade G1, 43% of grade G2. Grade G2 (p=0.004) and larger tumour infiltration (≥T4; p=0.03) correlated with lower survival. Hypoxic score 1 correlated with a greater tumour size (p=0.034), larger tumour infiltration (T3 or T4; p=0.001), grade G2 (p=0.046), presence of lymph node metastasis (p=0.0066) and with lower survival of patients (p=0.03).

Conclusion: The hypoxia-inducible factors CA9 and CXCR4 were found associated to the malignant progression of neuroendocrine tumours of the ileum. Their expression may reflect higher tumour aggressivity.

MeSH terms

  • Antigens, CD34 / metabolism
  • Antigens, Neoplasm / metabolism*
  • Carbonic Anhydrase IX
  • Carbonic Anhydrases / metabolism*
  • Cell Proliferation
  • Female
  • Gene Expression Regulation, Neoplastic / physiology*
  • Humans
  • Ileal Neoplasms / metabolism*
  • Ileal Neoplasms / mortality
  • Ileal Neoplasms / pathology
  • Ki-67 Antigen / metabolism
  • Longitudinal Studies
  • Male
  • Neovascularization, Pathologic / etiology
  • Neuroendocrine Tumors / metabolism*
  • Neuroendocrine Tumors / mortality
  • Neuroendocrine Tumors / pathology
  • Receptors, CXCR4 / metabolism*
  • Retrospective Studies
  • Survival Analysis
  • Survivors*

Substances

  • Antigens, CD34
  • Antigens, Neoplasm
  • CXCR4 protein, human
  • Ki-67 Antigen
  • Receptors, CXCR4
  • CA9 protein, human
  • Carbonic Anhydrase IX
  • Carbonic Anhydrases