[Mechanisms of preventive effect of tetrandrine on acquired multidrug resistance in K562 cells]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011 Apr;19(2):363-6.
[Article in Chinese]

Abstract

This study was purposed to explore the mechanisms of preventive effect of tetrandrine (TTD) on doxorubicin (ADM)-induced multidrug resistance (MDR) in human leukemia cell line K562 from two aspects of the transcription control of MDR1 gene and cell apoptosis. The experiment was divided into 3 groups: group I-blank control; group II-ADM-induced drug-resistance; group III-ADM-induced drug-resistance after pretreatment with TTD. Reverse transcription-PCR (RT-PCR) was used to detect the mRNA expression levels of c-Jun, YB-1 and Survivin genes. Western blot was used to determine the nuclear protein expression levels of c-Jun and YB-1. Flow cytometry was used to assay the apoptosis of cells. The results showed that as compared with group I, the expression levels of c-Jun mRNA and nuclear protein decreased (p < 0.05), as well as the expression levels of YB-1 mRNA and nuclear protein increased in group II (p < 0.05). However, the expression of Survivin mRNA had no change (p > 0.05); the apoptosis rate of cells was 8.31%. As compared with group II, the expression levels of c-Jun mRNA and nuclear protein increased (p < 0.05), expression levels of YB-1 mRNA and nuclear protein as well as Survivin mRNA decreased in group III (p < 0.05). The apoptosis of cells was 97.2%. It is concluded that TTD can inhibit the expression of YB-1 and up-regulate the expression of c-Jun, thus inhibit the expression of MDR1 gene. TTD can also inhibit the expression of Survivin and increase the apoptosis of cells induced by ADM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Benzylisoquinolines / pharmacology*
  • Drug Resistance, Multiple / drug effects*
  • Drug Resistance, Multiple / genetics
  • Drug Resistance, Neoplasm / drug effects*
  • Drug Resistance, Neoplasm / genetics
  • Humans
  • Inhibitor of Apoptosis Proteins / metabolism
  • K562 Cells
  • Proto-Oncogene Proteins c-jun / metabolism
  • Survivin
  • Y-Box-Binding Protein 1 / metabolism

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • BIRC5 protein, human
  • Benzylisoquinolines
  • Inhibitor of Apoptosis Proteins
  • Proto-Oncogene Proteins c-jun
  • Survivin
  • Y-Box-Binding Protein 1
  • YBX1 protein, human
  • tetrandrine