Frequent mutations of Ki-ras codon 12 in N-bis (2-hydroxypropyl)-nitrosamine-initiated thyroid, kidney and lung tumors in Wistar rats

Cancer Lett. 1995 Sep 25;96(2):155-61. doi: 10.1016/0304-3835(95)03932-m.

Abstract

N-Bis (2-hydroxypropyl) nitrosamine (DHPN) is a very potent mutagen and wide spectrum carcinogen in rodents. In the present study, we investigated mutational activation of the Ki-ras gene in eight thyroid, five kidney (four mesenchymal and one transitional cell lesion) and two lung tumors induced with DHPN. Mutations were identified using single-strand conformation polymorphism, restriction fragment length polymorphism and DNA sequencing analysis. All of the 15 neoplasms could be shown to have mutations in codon 12 (GGT-->GAT). These results suggest that Ki-ras mutations are frequent events during the development of DHPN-induced carcinomas in these organs. In a separate experiment, moreover, we analyzed the presence of Ki-ras mutations in various tissues 8 weeks after DHPN treatment. One of five thyroid tissues treated with DHPN was found to have the same characteristic mutation, suggesting that it may represent an early event during carcinogen-induced tumor formation in the thyroid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Carcinogens / toxicity*
  • Codon
  • DNA Primers
  • Deoxyribonucleases, Type II Site-Specific
  • Genes, ras / drug effects*
  • Kidney Neoplasms / chemically induced
  • Kidney Neoplasms / genetics*
  • Lung Neoplasms / chemically induced
  • Lung Neoplasms / genetics*
  • Male
  • Molecular Sequence Data
  • Mutagenesis*
  • Mutagens / toxicity*
  • Nitrosamines / toxicity*
  • Point Mutation*
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length*
  • Rats
  • Rats, Wistar
  • Thyroid Neoplasms / chemically induced
  • Thyroid Neoplasms / genetics*

Substances

  • Carcinogens
  • Codon
  • DNA Primers
  • Mutagens
  • Nitrosamines
  • diisopropanolnitrosamine
  • Deoxyribonucleases, Type II Site-Specific
  • GGTGA-specific type II deoxyribonucleases