Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells

Br J Cancer. 2012 Mar 13;106(6):1148-52. doi: 10.1038/bjc.2011.574. Epub 2012 Feb 16.

Abstract

Background: It is becoming increasingly recognised that opioids are responsible for tumour growth. However, the effects of opioids on tumour growth have been controversial.

Methods: The effects of κ-opioid receptor (KOR) agonist on the growth of non-small cell lung cancer (NSCLC) cells were assessed by a cell proliferation assay. Western blotting was performed to ascertain the mechanism by which treatment with KOR agonist suppresses tumour growth.

Results: Addition of the selective KOR agonist U50,488H to gefitinib-sensitive (HCC827) and gefitinib-resistant (H1975) NSCLC cells produced a concentration-dependent decrease in their growth. These effects were abolished by co-treatment with the selective KOR antagonist nor-BNI. Furthermore, the growth-inhibitory effect of gefitinib in HCC827 cells was further enhanced by co-treatment with U50,488H. With regard to the inhibition of tumour growth, the addition of U50, 488H to H1975 cells produced a concentration-dependent decrease in phosphorylated-glycogen synthase kinase 3β (p-GSK3β).

Conclusion: The present results showed that stimulation of KOR reduces the growth of gefitinib-resistant NSCLC cells through the activation of GSK3β.

MeSH terms

  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer / pharmacology*
  • Antineoplastic Agents / pharmacology
  • Carcinoma, Non-Small-Cell Lung
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Cell Survival
  • Drug Resistance, Neoplasm
  • ErbB Receptors / genetics
  • Gefitinib
  • Gene Expression
  • Glycogen Synthase Kinase 3 / metabolism
  • Glycogen Synthase Kinase 3 beta
  • Humans
  • Mutation, Missense
  • Naltrexone / analogs & derivatives
  • Naltrexone / pharmacology
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quinazolines / pharmacology
  • Receptors, Opioid, kappa / agonists*
  • Receptors, Opioid, kappa / antagonists & inhibitors
  • Receptors, Opioid, kappa / genetics
  • Receptors, Opioid, kappa / metabolism
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction

Substances

  • Antineoplastic Agents
  • Quinazolines
  • Receptors, Opioid, kappa
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • norbinaltorphimine
  • Naltrexone
  • 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
  • ErbB Receptors
  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta
  • Proto-Oncogene Proteins c-akt
  • Glycogen Synthase Kinase 3
  • Gefitinib