Menadione: spectrum of anticancer activity and effects on nucleotide metabolism in human neoplastic cell lines

Biochem Pharmacol. 1991 May 1;41(9):1283-92. doi: 10.1016/0006-2952(91)90099-q.


The spectrum of cytotoxicity of menadione (MD) was examined in a panel of human cancer cell lines. MD was equipotent against multidrug-resistant and parental leukemia cell lines with IC50 values of 13.5 +/- 3.6 and 18 +/- 2.4 microM respectively. A cervical carcinoma cell line resistant to the antimetabolite, methotrexate (MTX), was as sensitive to MD as its parental cell line. The interactions of fifteen clinically utilized anticancer drugs with MD were examined in vitro and the majority were found to be additive, with four agents exhibiting synergism and one agent exhibiting antagonism. MD inhibited the incorporation of radioactive thymidine, uridine and amino acids into DNA, RNA and protein, respectively, in three human cancer cell lines. Some possible reasons for the inhibition of DNA synthesis including effects of MD on intracellular deoxyribonucleoside triphosphate pools were examined and ruled out. Although results from previous studies using rat hepatocytes suggested that mitochondria may be a target of MD, no significant effect of this compound on total intracellular adenosine triphosphate (ATP) pools in human cancer cell lines was observed. Collectively, these in vitro results demonstrate that MD possesses a broad spectrum of anticancer activity and suggest the potential utility of this agent in cancer therapy. Future studies directed at elucidation of the mechanism of MD action in human cancer cells are warranted and are under study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents*
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology
  • Cell Survival / drug effects
  • DNA, Neoplasm / biosynthesis
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Humans
  • Neoplasms / metabolism*
  • Nucleotides / metabolism*
  • Tumor Cells, Cultured / drug effects
  • Vitamin K / pharmacology*


  • Antineoplastic Agents
  • DNA, Neoplasm
  • Nucleotides
  • Vitamin K