Triptolide induces cell death independent of cellular responses to imatinib in blast crisis chronic myelogenous leukemia cells including quiescent CD34+ primitive progenitor cells

Duncan H. Mak, Wendy D. Schober, Wenjing Chen, Marina Konopleva, Jorge Cortes, Hagop M. Kantarjian, Michael Andreeff, Bing Z. Carter

Research output: Contribution to journalArticle

28 Scopus citations

Abstract

The advent of Bcr-Abl tyrosine kinase inhibitors (TKI) has revolutionized the treatment of chronic myelogenous leukemia (CML). However,resistance evolves due to BCRABL mutations and other mechanisms. Furthermore, patients with blast crisis CML are less responsive and quiescent CML stem cells are insensitive to these inhibitors. We found that triptolide,a diterpenoid, at nanomolar concentrations, pro moted equally significant death of KBM5 cells,a cell line derived from a Bcr-Abl-bearing blast crisis CML patient and KBM5STI571 cells,an imatinib-resistant KBM5 subline bearing the T315I mutation. Similarly, Ba/F3 cells harboring mutated BCR-ABL were as sensitive as Ba/F3Bcr-Abl p210wt cells to triptolide. Importantly, triptolide induced apoptosis in primary samples from blast crisis CML patients,w ho showed resistance to Bcr-Abl TKIs in vivo,with less toxicity to normal cells. Triptolide decreased X-linked inhibitor of apoptosis protein, Mcl-1, and Bcr-Abl protein levels in K562, KBM5, and KBM5STI571 cells and in cells from blast crisis CML patients. It sensitized KBM5, but not KBM5STI571,ce lls to imatinib. More importantly, triptolide also induced death of quiescent CD34+ CML progenitor cells,a major problem in the therapy of CML with TKIs. Collectively, these results suggest that triptolide potently induces blast crisis CML cell death independent of the cellular responses to Bcr-Abl TKIs, suggesting that triptolide could eradicate residual quiescent CML progenitor cells in TKI-treated patients and benefit TKI-resistant blast crisis CML patients.

Original languageEnglish (US)
Pages (from-to)2509-2516
Number of pages8
JournalMolecular cancer therapeutics
Volume8
Issue number9
DOIs
StatePublished - Sep 1 2009

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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