Antitumor effects of an adenovirus expressing antisense insulin-like growth factor I receptor on human lung cancer cell lines

Cancer Res. 1996 Jul 1;56(13):3038-41.

Abstract

Insulin-like growth factors (IGFs) are often essential for the maintenance of the malignant phenotype, and in lung cancer the IGF-I receptor (IGF-Ir) is often expressed at high levels. Stable transfection of antisense plasmids expressing the first 300 bp of the IGF-Ir reduces the tumorigenicity of a variety of tumor cell lines and has been reported to induce systemic antitumor effects on established, non-gene-modified tumors in animal model systems. We have constructed an adenovirus expressing an antisense IGF-Ir (Ad-IGF-Ir/as) in an attempt to develop these observations into a clinical therapeutic approach. A single transduction by Ad-IGF-Ir/as (at a multiplicity of infection of 10:1) decreased the IGF-Ir number by about 50% in human lung cancer cell lines NCI H460 and SCC5, as measured by an 125I-labeled IGF-I competitive binding assay. After the transduction of these human lung cancer cell lines by Ad-IGF-Ir/as, the soft agar clonogenicity was reduced by 84%. The i.p. treatment of nude mice bearing established i.p. NCI H460 cells resulted in prolonged survival compared to that of nude mice treated with a reporter virus. These results suggest that Ad-IGF-Ir/as has a therapeutic effect on established human lung cancer xenografts and may represent an effective and practical cancer gene therapy strategy.

MeSH terms

  • Adenoviridae / genetics
  • Adenoviridae / metabolism
  • Agar
  • Animals
  • Base Sequence
  • Binding, Competitive
  • Carcinoma, Small Cell / genetics
  • Carcinoma, Small Cell / therapy*
  • Carcinoma, Small Cell / ultrastructure*
  • Cell Division / drug effects
  • Clone Cells
  • Female
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Iodine Radioisotopes
  • Lung Neoplasms / genetics
  • Lung Neoplasms / therapy*
  • Lung Neoplasms / ultrastructure*
  • Mice
  • Mice, Nude
  • Molecular Sequence Data
  • Neoplasm Transplantation
  • Oligonucleotides, Antisense / genetics*
  • Oligonucleotides, Antisense / metabolism*
  • Oligonucleotides, Antisense / pharmacology
  • Receptor, IGF Type 1 / biosynthesis
  • Receptor, IGF Type 1 / genetics*
  • Receptor, IGF Type 1 / metabolism*
  • Transduction, Genetic
  • Transfection
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

Substances

  • Iodine Radioisotopes
  • Oligonucleotides, Antisense
  • Insulin-Like Growth Factor I
  • Agar
  • Receptor, IGF Type 1