MDR-1 gene expression is a minor factor in determining the multidrug resistance phenotype of MCF7/ADR and KB-V1 cells

FEBS Lett. 1997 Jul 21;412(1):201-6. doi: 10.1016/s0014-5793(97)00777-1.

Abstract

The relevance of MDR-1 gene expression to the multidrug resistance phenotype was investigated. Drug-resistant cells, KB-V1 and MCF7/ADR, constantly expressed mRNA of the MDR-1 gene and were more resistant to vinblastine and adriamycin than drug-sensitive cells, KB-3-1 and MCF7. The drug efflux rate of KB-V1 was the same as KB-3-1 although the MDR-1 gene was expressed in only the resistant cell. The higher intracellular drug concentration of KB-3-1 than KB-V1 was due to the large drug influx. In the case of MCF7 and MCF7/ADR, the influx and efflux of the drug had nearly the same pattern and drug efflux was not affected by verapamil. The amount of ATP, cofactor of drug pumping activity of P-glycoprotein, was not changed by the resistance. These observations suggested that drug efflux mediated by MDR-1 gene expression was not a major determining factor of drug resistance in the present cell systems, and that the drug resistance could be derived from the change in drug uptake and other mechanisms.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics*
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Adenosine Triphosphate / metabolism
  • Antineoplastic Agents / pharmacology
  • Calcium Channel Blockers / pharmacology
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple / genetics*
  • Gene Expression*
  • Glyceraldehyde-3-Phosphate Dehydrogenases / genetics
  • Humans
  • Phenotype
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured
  • Verapamil / pharmacology
  • Vinblastine / pharmacology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antineoplastic Agents
  • Calcium Channel Blockers
  • RNA, Messenger
  • Vinblastine
  • Doxorubicin
  • Adenosine Triphosphate
  • Verapamil
  • Glyceraldehyde-3-Phosphate Dehydrogenases