DNA Damage in the Intracerebral Rat Gliosarcoma 9L Treated with 1-(2-Chloroethyl)-3-cyclohexyl-1-nitrosourea Academic Article uri icon

Overview

MeSH Major

  • Brain Neoplasms
  • DNA, Neoplasm
  • Glioma
  • Lomustine
  • Nitrosourea Compounds

abstract

  • Nitrosoureas are among the most effective agents for brain tumor chemotherapy, but their mode of action is uncertain. Damage to DNA in the intracerebral rat gliosarcoma 9L following in vivo exposure to 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) was determined by the alkaline sucrose gradient method. Following i.p. CCNU treatment, tumors were removed and mechanically dissociated. Tumor cells were lysed upon and sedimented through an alkaline sucrose gradient. DNA content of gradient fractions was assayed fluorometrically. DNA from tumor cells exposed to therapeutic, nontoxic CCNU doses sedimented more slowly than did untreated DNA, indicating single-strand breaks or alkali-labile strand damage. At this nontoxic dose and at short lysis times, anomalous sedimentation was observed, while conventional random sedimentation profiles were attained with the increased damage from higher doses. Damage to tumor DNA was also investigated by measuring the fraction of DNA remaining double stranded after exposure to alkali by determining its resistance to Si nuclease from Aspergillus oryzae. This fraction reflects its counterpart, the fraction of DNA that has completely unwound between single-strand breaks and separated irreversibly from the helix, and thus gives quantitative insight into the amount of damage present. Tumors from rats receiving a 3-hr treatment with CCNU (30 mg/kg) or methyl methanesulfonate (25 mg/kg) showed equivalent fractions of double-stranded DNA in alkali. The double-stranded DNA fraction for tumors treated with methyl methanesulfonate returned to control levels by 16 hr, demonstrating complete repair of the rat brain tumor DNA in vivo. CCNU-treated tumors showed no detectable ability to repair the damage by 16 hr. © 1977, American Association for Cancer Research. All rights reserved.

publication date

  • January 1977

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed ID

  • 908019

Additional Document Info

start page

  • 3761

end page

  • 5

volume

  • 37

number

  • 10