Glioma cell sensitivity to topotecan: the role of p53 and topotecan-induced DNA damage

Eur J Pharmacol. 2001 Jan 19;412(1):21-5. doi: 10.1016/s0014-2999(00)00923-7.

Abstract

Topotecan is a topoisomerase I inhibitor which is currently evaluated as an adjuvant agent for malignant glioma. Here, we analysed the effects of topotecan on 12 human malignant glioma cell lines in vitro. All cell lines expressed topoisomerase I mRNA. High p53 protein levels, but not genetic or functional p53 status, were associated with increased topotecan-induced DNA/topoisomerase I complex formation. Neither functional p53 status, nor p53 protein levels, nor complex formation predicted topotecan-induced growth inhibition. We thus confirm a possible role for p53 protein in modulating topoisomerase I activity but conclude that the major molecular determinants of topotecan sensitivity in glioma cells await identification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • DNA Damage / drug effects*
  • DNA Damage / physiology
  • DNA Topoisomerases, Type I / drug effects*
  • DNA Topoisomerases, Type I / metabolism
  • DNA, Neoplasm / drug effects*
  • Genes, p53 / drug effects*
  • Genes, p53 / physiology
  • Glioma / metabolism*
  • Humans
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Topotecan / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • DNA, Neoplasm
  • RNA, Messenger
  • Topotecan
  • DNA Topoisomerases, Type I