Activation and overexpression of centrosome kinase BTAK/Aurora-A in human ovarian cancer

Clin Cancer Res. 2003 Apr;9(4):1420-6.

Abstract

Previous studies have demonstrated amplification of the centrosome serine/threonine kinase BTAK/Aurora-A in 10-25% of ovarian cancers. However, alterations of BTAK/Aurora-A at kinase and protein levels and its role in ovarian cancer progression have not been well documented. In this study, we examined the kinase activity and protein levels of BTAK/Aurora-A in 92 patients with primary ovarian tumors. In vitro kinase analyses revealed elevated BTAK/Aurora-A kinase activity in 44 cases (48%). Increased BTAK/Aurora-A protein levels were detected in 52 (57%) specimens. High protein levels of BTAK/Aurora-A correlated well with elevated kinase activity. Activation and overexpression of BTAK/Aurora-A were more frequently detected in early stage/low-grade ovarian tumors, although there was no statistic significance at the kinase level between early stage/low-grade and late stage/high-grade tumors. Moreover, BTAK/Aurora-A was preferentially expressed in noninvasive tumors, as revealed by immunohistochemical staining, suggesting that alterations of BTAK/Aurora-A could be an early event in human ovarian oncogenesis. To our knowledge, this is the first demonstration of recurrent activation and overexpression of BTAK/Aurora-A in human ovarian cancer, which may play a critical role in development of this malignancy.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aurora Kinase A
  • Aurora Kinases
  • Blotting, Northern
  • Blotting, Southern
  • Blotting, Western
  • Cell Line
  • DNA, Complementary / metabolism
  • Female
  • Glutathione Transferase / metabolism
  • Humans
  • Immunohistochemistry
  • Ovarian Neoplasms / enzymology*
  • Ovarian Neoplasms / metabolism
  • Ovary / metabolism
  • Precipitin Tests
  • Protein Serine-Threonine Kinases / biosynthesis*
  • Protein Serine-Threonine Kinases / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Transfection

Substances

  • DNA, Complementary
  • Recombinant Fusion Proteins
  • Glutathione Transferase
  • AURKA protein, human
  • Aurora Kinase A
  • Aurora Kinases
  • Protein Serine-Threonine Kinases