Effects of combination of notch inhibitor plus hedgehog inhibitor or Wnt inhibitor on growth of leukemia cells

Anticancer Res. 2011 Mar;31(3):893-6.

Abstract

Background: The Notch inhibitors, γ-secretase inhibitors (GSIs), are promising candidates for molecular targeted therapy against leukemia. However, they show only limited effectiveness. We thought that the efficacy of GSIs might be improved by their combination with Hedgehog inhibitors and Wnt inhibitors because these signaling pathways are also important for the growth of leukemia cells.

Materials and methods: The effects of the combination of GSI-XXI plus the Hedgehog inhibitor, cyclopamine (Cy), or the Wnt inhibitor, quercetin (Qu), on the in vitro cell growth, colony formation and Notch1 protein expression of three T-cell acute lymphoblastic leukemia (T-ALL) cell lines with NOTCH1 mutations and three acute myeloid leukemia cell lines were examined.

Results: The addition of Cy or Qu to GSI suppressed the growth of DND-41 T-ALL cells additively or synergistically, respectively. Interestingly, Cy treatment and Qu treatment reduced Notch1 protein and its active fragment in DND-41 cells, which suggests a relationship between Notch signaling and Hedgehog or Wnt signaling. The addition of Cy or Qu to GSI promoted the decrease of Notch1 activation and expression.

Conclusion: The anti-leukemic effects of a GSI could be promoted by its combination with Cy or Qu, in appropriate cases selected by in vitro drug sensitivity test.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Dibenzazepines / pharmacology
  • Drug Synergism
  • Hedgehog Proteins / antagonists & inhibitors*
  • Hedgehog Proteins / metabolism
  • Humans
  • Leukemia / pathology*
  • Quercetin / pharmacology
  • Receptors, Notch / antagonists & inhibitors*
  • Receptors, Notch / metabolism
  • Tumor Stem Cell Assay
  • Veratrum Alkaloids / pharmacology
  • Wnt Proteins / antagonists & inhibitors*
  • Wnt Proteins / metabolism

Substances

  • Antineoplastic Agents
  • Dibenzazepines
  • Hedgehog Proteins
  • Receptors, Notch
  • Veratrum Alkaloids
  • Wnt Proteins
  • Quercetin
  • dibenzazepine
  • cyclopamine