Biological activity of hydroxylated chloroethylnitrosoureas

Cancer Res. 1989 Jun 15;49(12):3267-70.

Abstract

1-Nitroso-1-(2-hydroxyethyl)-3-(2-chloroethyl)urea (Compound I) and 1-nitroso-1-(2-hydroxypropyl)-3-(2-chloroethyl)urea (Compound II) display significantly reduced antitumor activity compared to the corresponding isomeric derivatives 1-nitroso-1-(2-chloroethyl)-3-(2-hydroxyethyl) urea (Compound III) and 1-nitroso-1-(2-chloroethyl)-3-(2-hydroxypropyl) urea (Compound IV). Their low therapeutic activity is paralleled by low toxicity while mutagenicity and carcinogenicity are high. A comparative investigation of the genotoxicity of Compounds I and III using primary cultures of fetal hamster lung cells revealed an about 14-fold higher rate of DNA single-strand breaks following exposure (100 microM, 1 h) to Compound I as compared to Compound III. The rate of DNA interstrand cross-links, on the other hand, was 11-fold higher following Compound III as compared to Compound I. The results underline that the therapeutic activity of chloroethylnitrosoureas is mainly attributable to their cross-linking potential while induction of DNA single-strand breaks plays a decisive role for mutagenicity and carcinogenicity but appears not to be relevant for antineoplastic effectiveness.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Drug Evaluation, Preclinical
  • Female
  • Leukemia L1210 / drug therapy*
  • Leukemia, Experimental / drug therapy*
  • Mice
  • Mice, Inbred Strains
  • Nitrosourea Compounds / therapeutic use*
  • Rats
  • Rats, Inbred Strains
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Nitrosourea Compounds
  • 1-nitroso-1-(2-chloroethyl)-3-(2-hydroxypropyl)urea
  • 1-nitroso-1-(2-hydroxyethyl)-3-(2-chloroethyl)urea
  • 1-nitroso-1-(2-hydroxypropyl)-3-(2-chloroethyl)urea
  • elmustine