Expression and heterodimer-binding activity of Ku70 and Ku80 in human non-melanoma skin cancer

J Clin Pathol. 2006 Nov;59(11):1181-5. doi: 10.1136/jcp.2005.031088. Epub 2006 Feb 23.

Abstract

Background: Experimental data suggest that exposure to ultraviolet radiation may indirectly induce DNA double-strand breaks.

Aim: To investigate the contribution of the non-homologous end-joining repair pathway in basal and squamous cell carcinomas.

Methods: Levels of Ku70 and Ku80 proteins were determined by immunohistochemical analysis and Ku70-Ku80 heterodimer-binding activity by electrophoretic mobility shift assay. Matched pathological normal margins and skin from healthy people were used as controls.

Results: A significant increase in Ku70 and Ku80 protein levels was found for both tumour types as compared with normal skin (p<0.001). Squamous cell carcinoma showed increased immunostaining as compared with basal cell tumours (p<0.02). A direct correlation was found between Ku70 and Ku80 protein levels and expression of the proliferation markers Ki-67/MIB-1 (p<0.02 and p<0.002, respectively) in basal cell carcinoma. DNA binding activity was increased in basal cell carcinoma samples as compared with matched skin histopathologically negative for cancer (p<0.006). In squamous cell carcinomas, however, the difference was significant only with normal skin (p<0.02) and not with matched pathologically normal margins.

Conclusions: Overall, an up regulation of the Ku70 and Ku80 protein levels seems to correlate only with tumour proliferation rate. As non-homologous end joining is an error-prone mechanism, its up regulation may ultimately increase genomic instability, contributing to tumour progression.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Nuclear / metabolism*
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Basal Cell / metabolism*
  • Carcinoma, Basal Cell / pathology
  • Carcinoma, Squamous Cell / metabolism*
  • Carcinoma, Squamous Cell / pathology
  • Cell Proliferation
  • DNA-Binding Proteins / metabolism*
  • Disease Progression
  • Electrophoretic Mobility Shift Assay
  • Humans
  • Ki-67 Antigen / metabolism
  • Ku Autoantigen
  • Neoplasm Proteins / metabolism
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / pathology
  • Up-Regulation

Substances

  • Antigens, Nuclear
  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • Ki-67 Antigen
  • Neoplasm Proteins
  • Xrcc6 protein, human
  • Ku Autoantigen