Doxorubicin resistance in human melanoma cells: MDR-1 and glutathione S-transferase pi gene expression

Biochem Pharmacol. 1993 Feb 9;45(3):743-51. doi: 10.1016/0006-2952(93)90150-u.

Abstract

Cellular drug resistance is believed to involve P-glycoprotein-related drug efflux as well as xenobiotic detoxification. In the present study, we analyzed five human melanoma cell lines with 1- to 6-fold doxorubicin resistance for doxorubicin retention and MDR-1 and GST pi gene expression. All the cell lines had high doxorubicin retention, and efflux blockers such as trifluoperazine and verapamil did not have a major effect on drug retention or cytotoxicity. Even though all the cell lines carried the MDR-1 and GST pi genes, gene amplification was not associated with drug resistance. Both laser flow cytometry and immunoperoxidase staining showed high expression of C-219 reactive P-glycoprotein in some of the resistant cells which was not accompanied by either high drug efflux or sensitivity to doxorubicin efflux blockers.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Animals
  • Cell Death / drug effects
  • Cell Division / drug effects
  • Cell Line / drug effects
  • Cricetinae
  • Cricetulus
  • Dose-Response Relationship, Drug
  • Doxorubicin / pharmacology*
  • Drug Resistance / genetics
  • Gene Expression
  • Glutathione Transferase / analysis*
  • Glutathione Transferase / genetics
  • Humans
  • Leukemia P388 / genetics
  • Melanoma / genetics*
  • Membrane Glycoproteins / analysis*
  • Membrane Glycoproteins / genetics
  • Mice
  • RNA, Messenger / analysis
  • Trifluoperazine / pharmacology
  • Tumor Cells, Cultured / drug effects
  • Verapamil / pharmacology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Membrane Glycoproteins
  • RNA, Messenger
  • Trifluoperazine
  • Doxorubicin
  • Verapamil
  • Glutathione Transferase