Combinatorial antileukemic disruption of oxidative homeostasis and mitochondrial stability by the redox reactive thalidomide 2-(2,4-difluoro-phenyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3(2H)-dione (CPS49) and flavopiridol

Mol Pharmacol. 2008 Sep;74(3):872-83. doi: 10.1124/mol.107.040808. Epub 2008 Jun 12.

Abstract

2-(2,4-Difluoro-phenyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3(2H)-dione (CPS49) is a member of a recently identified class of redox-reactive thalidomide analogs that show selective killing of leukemic cells by increasing intracellular reactive oxygen species (ROS) and targeting multiple transcriptional pathways. Flavopiridol is a semisynthetic flavonoid that inhibits cyclin-dependent kinases and also shows selective lethality against leukemic cells. The purpose of this study is to explore the efficacy and mechanism of action of the combinatorial use of the redox-reactive thalidomide CPS49 and the cyclin-dependent kinase inhibitor flavopiridol as a selective antileukemic therapeutic strategy. In combination, CPS49 and flavopiridol were found to induce selective cytotoxicity associated with mitochondrial dysfunction and elevations of ROS in leukemic cells ranging from additive to synergistic activity at low micromolar concentrations. Highest synergy was observed at the level of ROS generation with a strong correlation between cell-specific cytotoxicity and reciprocal coupling of drug-induced ROS elevation with glutathione depletion. Examination of the transcriptional targeting of CPS49 and flavopiridol combinations reveals that the drugs act in concert to initiate a cell specific transcriptional program that manipulates nuclear factor-kappaB (NF-kappaB), E2F-1, and p73 activity to promote enhanced mitochondrial instability by simultaneously elevating the expression of the proapoptotic factors BAX, BAD, p73, and PUMA while depressing expression of the antiapoptotic genes MCL1, XIAP, BCL-xL, SURVIVIN, and MDM2. The coadministration of CPS49 and flavopiridol acts through coordinate targeting of transcriptional pathways that enforce selective mitochondrial dysfunction and ROS elevation and is therefore a promising new therapeutic combination that warrants further preclinical exploration.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Apoptosis Regulatory Proteins / metabolism
  • Cell Death / drug effects
  • Cell Line, Tumor
  • DNA-Binding Proteins / metabolism
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Drug Synergism
  • Flavonoids / pharmacology*
  • Free Radical Scavengers / pharmacology
  • Glutathione / metabolism
  • Homeostasis / drug effects*
  • Humans
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Leukemia / pathology*
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects*
  • NF-kappa B / metabolism
  • Nuclear Proteins / metabolism
  • Organ Specificity / drug effects
  • Oxidation-Reduction / drug effects
  • Piperidines / pharmacology*
  • Proto-Oncogene Proteins / metabolism
  • Reactive Oxygen Species / metabolism
  • Thalidomide / analogs & derivatives*
  • Thalidomide / pharmacology
  • Transcription, Genetic / drug effects
  • Tumor Suppressor Proteins / metabolism

Substances

  • Antineoplastic Agents
  • Apoptosis Regulatory Proteins
  • BBC3 protein, human
  • CPS 49
  • DNA-Binding Proteins
  • Flavonoids
  • Free Radical Scavengers
  • NF-kappa B
  • Nuclear Proteins
  • Piperidines
  • Proto-Oncogene Proteins
  • Reactive Oxygen Species
  • Tumor Suppressor Proteins
  • alvocidib
  • Thalidomide
  • Glutathione