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Anti-proliferative effect of the abl tyrosine kinase inhibitor STI571 on the P-glycoprotein positive K562/ADM cell line

  • Mitsuko Kotaki
  • , Toshiko Motoji*
  • , Minoko Takanashi
  • , Yan Hua Wang
  • , Hideaki Mizoguchi
  • *Corresponding author for this work
  • Tokyo Women's Medical University
  • Tokyo Metropol. Red Cross Blood Ctr.

Research output: Contribution to journalArticlepeer-review

Abstract

STI571, an abl tyrosine kinase inhibitor, is less effective in chronic myelogenous leukemia (CML) patients in the accelerated phase and in blastic crisis. We addressed whether STI571 is effective for the CML blastic crisis cell line K562 and the P-glycoprotein (P-gp) positive, multidrug resistance cell line K562/ADM. The present results demonstrate that P-gp positive K562/ADM cells were more resistant than K562 cells to the anti-proliferative and apoptotic effect of STI571, but the co-addition of a P-gp modulator augmented the sensitivity of K562/ADM cells to STI571. For patients in CML blastic crisis, simultaneous use of a P-gp modulator may increase the efficacy of STI571.

Original languageEnglish
Pages (from-to)61-68
Number of pages8
JournalCancer Letters
Volume199
Issue number1
DOIs
Publication statusPublished - 10 Sept 2003
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • K562 cell line
  • MS-209
  • Multidrug resistance
  • P-glycoprotein
  • STI571

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