Reversal of drug resistance mediated by hammerhead ribozyme against multidrug resistance-associated protein 1 in a human glioma cell line

Int J Oncol. 2003 Apr;22(4):823-7.

Abstract

We examined the effects of suppressing multidrug resistance-associated protein 1 (MRP1) gene expression in a human glioma cell line U87MG. Hammerhead ribozymes, designed to cleave MRP1 mRNA (alphaMRP1-Rz), were transfected into the U87MG cells. The U87MG/alphaMRP1-Rz cells were significantly sensitive to nitrosourea (ACNU) and doxorubicin (DOX) compared with the U87MG cells (p<0.01 and p<0.05, respectively, unpaired t-test). There was no significant difference in the expression of other human genes between the U87MG/alphaMRP1-Rz and controls by cDNA array. The hammerhead ribozyme-mediated specific suppression of MRP1 was sufficient to reverse the resistance of ACNU and DOX in the human glioma cell line.

MeSH terms

  • Antibiotics, Antineoplastic / pharmacology
  • Blotting, Northern
  • Cell Division
  • Cell Line, Tumor
  • Cell-Free System
  • Coloring Agents / pharmacology
  • DNA, Complementary / metabolism
  • Doxorubicin / pharmacology
  • Drug Resistance, Multiple*
  • Gene Expression Regulation
  • Humans
  • Inhibitory Concentration 50
  • Nitrosourea Compounds / pharmacology
  • Oligonucleotide Array Sequence Analysis
  • RNA, Catalytic* / chemistry
  • RNA, Catalytic* / metabolism
  • RNA, Messenger / metabolism
  • Tetrazolium Salts / pharmacology
  • Thiazoles / pharmacology
  • Transfection

Substances

  • Antibiotics, Antineoplastic
  • Coloring Agents
  • DNA, Complementary
  • Nitrosourea Compounds
  • RNA, Catalytic
  • RNA, Messenger
  • Tetrazolium Salts
  • Thiazoles
  • hammerhead ribozyme
  • Doxorubicin
  • thiazolyl blue