Elevated epidermal growth factor receptor binding in plutonium-induced lung tumors from dogs

Proc Soc Exp Biol Med. 1991 Apr;196(4):385-9. doi: 10.3181/00379727-196-43203.

Abstract

The objective of this study is to examine and characterize epidermal growth factor receptor (EGF-R) binding in inhaled plutonium-induced canine lung-tumor tissue and to compare it with that in normal canine lung tissue. Crude membrane preparations from normal and lung-tumor tissue from beagle dogs were examined in a radioreceptor assay, using 125I-labeled epidermal growth factor (EGF) as a ligand. Specific EGF receptor binding was determined in the presence of excess unlabeled EGF. We have examined EGF receptor binding in eight lung-tumor samples obtained from six dogs. Epidermal growth factor receptor binding was significantly greater in lung-tumor samples (31.38%) compared with that in normal lung tissue (3.76%). Scatchard plot analysis from the displacement assay revealed that there was no statistical difference in the binding affinity but significantly higher concentration of EGF-R sites in the lung-tumor tissue (619 fmol/mg) than in normal lung tissue (53 fmol/mg). The increase in EGF-R number in plutonium-induced dog lung tumors does not seem to correlate with increase in the initial lung burden exposure to plutonium. Our results demonstrate that there is a significant increase in EGF-R binding in inhaled plutonium-induced dog lung tumors.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adenocarcinoma, Papillary / metabolism*
  • Administration, Inhalation
  • Animals
  • Binding, Competitive
  • Carcinoma, Bronchogenic / metabolism*
  • Dogs
  • Epidermal Growth Factor / metabolism
  • ErbB Receptors / metabolism*
  • Female
  • In Vitro Techniques
  • Lung Neoplasms / etiology
  • Lung Neoplasms / metabolism*
  • Male
  • Membrane Proteins / metabolism
  • Neoplasms, Radiation-Induced
  • Plutonium*
  • Radioligand Assay

Substances

  • Membrane Proteins
  • Plutonium
  • Epidermal Growth Factor
  • ErbB Receptors