Chemosensitization of human prostate cancer using antisense agents targeting the type 1 insulin-like growth factor receptor

BJU Int. 2003 Feb;91(3):271-7. doi: 10.1046/j.1464-410x.2003.04061.x.

Abstract

Objective: To assess the effect of the downregulation of type 1 insulin-like growth factor receptor (IGF1R) on the chemosensitivity of prostate cancer cells. IGF1R is overexpressed by prostate cancer compared with benign prostatic epithelium and IGF1R expression commonly persists in androgen-independent metastatic disease at levels comparable to those in the primary.

Materials and methods: Human androgen-independent DU145 prostate cancer cells were transfected with IGF1R antisense oligonucleotides or antisense RNA. Transfected cultures were treated with cisplatin, mitoxantrone, paclitaxel or vehicle control, and survival measured using a clonogenic assay.

Results: Both antisense strategies suppressed IGF1R protein levels to 30-50% of those in control cultures. This was associated with 1.5-2-fold enhancement of sensitivity to cisplatin, mitoxantrone and paclitaxel, and an increase in cisplatin-induced apoptosis.

Conclusion: This approach has potential for development as a clinical treatment for advanced prostate cancer and other chemoresistant tumours.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects
  • Cisplatin / therapeutic use
  • Down-Regulation
  • Humans
  • Male
  • Mitoxantrone / therapeutic use
  • Oligonucleotides, Antisense / genetics
  • Oligonucleotides, Antisense / therapeutic use*
  • Paclitaxel / therapeutic use
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / therapy
  • Receptor, IGF Type 1 / metabolism*
  • Transfection
  • Tumor Cells, Cultured / drug effects
  • Tumor Stem Cell Assay

Substances

  • Antineoplastic Agents
  • Oligonucleotides, Antisense
  • Mitoxantrone
  • Receptor, IGF Type 1
  • Paclitaxel
  • Cisplatin