Topoisomerase IIalpha in Wilms' tumour: gene alterations and immunoexpression

J Clin Pathol. 2006 Dec;59(12):1272-7. doi: 10.1136/jcp.2005.031963. Epub 2006 Mar 23.

Abstract

Background: Topoisomerase IIalpha (topoIIalpha) is an essential enzyme gene in regulating DNA structure and cell proliferation and is encoded by the TOP2A. Using cDNA microarray analysis, TOP2A has been reported to be one of the top genes overexpressed in Wilms' tumour.

Aim: To evaluate the role of TopoIIalpha in Wilms' tumorigenesis and its prognostic value.

Methods: TOP2A gene copy numbers were determined using the fluorescence in situ hybridisation technique, and protein expression levels of TopoIIalpha by immunostaining in 39 samples of primary and 18 samples of metastatic Wilms' tumour.

Results: TOP2A gene amplification was detected only in anaplastic Wilms' tumours, and none of the Wilms' tumours showed deletion of the TOP2A gene. TopoIIalpha protein overexpression was detected in 97% of Wilms' tumours, and correlated strongly with proliferation, as measured by Ki-67 (r = 0.85). The high TopoIIalpha expression was associated with the presence of vascular invasion, prominent apoptosis, metastases and adverse clinical outcomes (p<0.05).

Conclusions: Our findings suggest that TopoIIalpha overexpression in Wilms' tumours is caused by a change at the transcription level, except for anaplastic Wilms' tumours, in which gene amplification was present. High levels of TopoIIalpha protein are correlated with tumour aggressiveness. The assessment of TopoIIalpha expression in Wilms' tumour may have prognostic value.

MeSH terms

  • Antigens, Neoplasm / genetics*
  • Antigens, Neoplasm / metabolism
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Child
  • Child, Preschool
  • DNA Topoisomerases, Type II / genetics*
  • DNA Topoisomerases, Type II / metabolism
  • DNA, Neoplasm / genetics
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Female
  • Humans
  • Immunoenzyme Techniques / methods
  • In Situ Hybridization, Fluorescence / methods
  • Infant
  • Ki-67 Antigen / metabolism
  • Kidney Neoplasms / enzymology
  • Kidney Neoplasms / genetics*
  • Kidney Neoplasms / pathology
  • Male
  • Neoplasm Staging
  • Oligonucleotide Array Sequence Analysis / methods
  • Poly-ADP-Ribose Binding Proteins
  • Prognosis
  • Survival Analysis
  • Wilms Tumor / enzymology
  • Wilms Tumor / genetics*
  • Wilms Tumor / pathology
  • Wilms Tumor / secondary

Substances

  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • DNA, Neoplasm
  • DNA-Binding Proteins
  • Ki-67 Antigen
  • Poly-ADP-Ribose Binding Proteins
  • DNA Topoisomerases, Type II
  • TOP2A protein, human