EBNA1 may prolong G(2)/M phase and sensitize HER2/neu-overexpressing ovarian cancer cells to both topoisomerase II-targeting and paclitaxel drugs

Biochem Biophys Res Commun. 2003 Aug 1;307(3):653-9. doi: 10.1016/s0006-291x(03)01235-x.

Abstract

We have shown previously that the Epstein-Barr virus nuclear antigen-1 (EBNA1) can act as a transforming suppressor in the HER2/neu-overexpressing ovarian cancer cells. In the present study, by using flow cytometric analysis, we demonstrate that EBNA1 could prolong G(2)/M phase and sensitize to Taxol-induced apoptosis in the EBNA1-expressing ovarian cancer cell stable transfectants. In addition, EBNA1 could also significantly increase topoisomerase IIalpha protein expression, indicating that the up-regulation of topoisomerase IIalpha may be one of the mechanisms by which EBNA1 enhances the sensitivity of ovarian cancer cells to topoisomerase II-targeting anticancer drugs, such as VP-16 and Adriamycin. These data suggest that EBNA1 not only prolongs cell cycle at G(2)/M phase and up-regulates topoisomerase IIalpha expression in HER2/neu-overexpressing ovarian cancer cells, but also increases cellular apoptosis through sensitization of cancer cells to topoisomerase II-directing anticancer drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Neoplasm
  • Antineoplastic Agents / therapeutic use*
  • Apoptosis
  • Carcinoma / drug therapy
  • Carcinoma / metabolism
  • Carcinoma / therapy
  • DNA Topoisomerases, Type II
  • DNA-Binding Proteins
  • Down-Regulation
  • Doxorubicin / therapeutic use
  • Drug Delivery Systems
  • Drug Therapy, Combination
  • Epstein-Barr Virus Nuclear Antigens / genetics*
  • Etoposide / therapeutic use
  • Female
  • G2 Phase
  • Genetic Therapy
  • Humans
  • Kinetics
  • Mitosis
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / therapy*
  • Paclitaxel / therapeutic use*
  • Receptor, ErbB-2 / metabolism*
  • Topoisomerase II Inhibitors*
  • Tumor Cells, Cultured

Substances

  • Antigens, Neoplasm
  • Antineoplastic Agents
  • DNA-Binding Proteins
  • Epstein-Barr Virus Nuclear Antigens
  • Topoisomerase II Inhibitors
  • Etoposide
  • Doxorubicin
  • Receptor, ErbB-2
  • DNA Topoisomerases, Type II
  • EBV-encoded nuclear antigen 1
  • Paclitaxel