Interleukin-6 is responsible for drug resistance and anti-apoptotic effects in prostatic cancer cells

Prostate. 2004 Jul 1;60(2):120-9. doi: 10.1002/pros.20057.

Abstract

Background: Interleukin (IL)-6-mediated anti-apoptotic effects and drug-resistance mechanisms in prostate cancer cells were investigated.

Methods: IL-6 levels of PC-3 and LNCaP cells were studied by using ELISA. Protective effects of IL-6 on cytotoxic agent-induced apoptosis were studied by exogenous IL-6 in serum-starved PC-3 cells and by anti-sense IL-6 strategy. Western blotting and reverse transcription-polymerase chain reaction (RT-PCR) were used to determine IL-6 effects on Bcl-2 family proteins. Tetracycline-regulated Bcl-xL expression system and dominant negative STAT3 transfectants were used to study IL-6 signaling pathways and its anti-apoptosis effects.

Results: Exogenous IL-6 and anti-sense IL-6 oligonucleotide treatment conferred resistance to cytotoxic agent-induced apoptosis. Among Bcl-2 family proteins, only Bcl-xL was evidently increased by IL-6 stimulation. The anti-apoptotic effect of IL-6 can be significantly attenuated by anti-sense bcl-xL transfection and partially abrogated in dominant negative STAT3 transfectants.

Conclusions: IL-6 is a survival factor against cytotoxic agent-induced apoptosis through both STAT3 and bcl-xL pathways in prostate cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / genetics
  • Acute-Phase Proteins / pharmacology
  • Apoptosis / drug effects*
  • Apoptosis / genetics*
  • Blotting, Western
  • Cell Survival
  • DNA-Binding Proteins / pharmacology
  • Drug Resistance, Neoplasm
  • Enzyme-Linked Immunosorbent Assay
  • Gene Expression Profiling
  • Humans
  • Interleukin-6 / pharmacology*
  • Male
  • Oligonucleotides, Antisense / therapeutic use
  • Prostatic Neoplasms / pathology*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT3 Transcription Factor
  • Trans-Activators / pharmacology
  • Tumor Cells, Cultured
  • bcl-X Protein

Substances

  • Acute-Phase Proteins
  • BCL2L1 protein, human
  • DNA-Binding Proteins
  • Interleukin-6
  • Oligonucleotides, Antisense
  • Proto-Oncogene Proteins c-bcl-2
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Trans-Activators
  • bcl-X Protein