5-azacytidine and decitabine exert proapoptotic effects on neoplastic mast cells: role of FAS-demethylation and FAS re-expression, and synergism with FAS-ligand

Blood. 2012 May 3;119(18):4242-52. doi: 10.1182/blood-2011-09-382770. Epub 2012 Mar 21.

Abstract

Aggressive systemic mastocytosis (ASM) and mast cell leukemia (MCL) are advanced hematopoietic neoplasms with poor prognosis. In these patients, neoplastic mast cells (MCs) are resistant against various drugs. We examined the effects of 2 demethylating agents, 5-azacytidine and decitabine on growth and survival of neoplastic MCs and the MC line HMC-1. Two HMC-1 subclones were used, HMC-1.1 lacking KIT D816V and HMC-1.2 exhibiting KIT D816V. Both agents induced apoptosis in HMC-1.1 and HMC-1.2 cells. Decitabine, but not 5-azacytidine, also produced a G(2)/M cell-cycle arrest in HMC-1 cells. Drug-induced apoptosis was accompanied by cleavage of caspase-8 and caspase-3 as well as FAS-demethylation and FAS-re-expression in neoplastic MCs. Furthermore, both demethylating agents were found to synergize with the FAS-ligand in inducing apoptosis in neoplastic MCs. Correspondingly, siRNA against FAS was found to block drug-induced expression of FAS and drug-induced apoptosis in HMC-1 cells. Neither 5-azacytidine nor decitabine induced substantial apoptosis or growth arrest in normal MCs or normal bone marrow cells. Together, 5-azacytidine and decitabine exert growth-inhibitory and proapoptotic effects in neoplastic MCs. These effects are mediated through "FAS-re-expression" and are augmented by the FAS-ligand. Whether epigenetic drugs produce antineoplastic effects in vivo in patients with ASM and MCL remains to be determined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antimetabolites, Antineoplastic / pharmacology*
  • Apoptosis / drug effects*
  • Azacitidine / analogs & derivatives*
  • Azacitidine / pharmacology*
  • Base Sequence
  • Cell Line, Tumor / drug effects
  • CpG Islands
  • DNA Methylation / drug effects
  • DNA, Neoplasm / metabolism
  • Decitabine
  • Drug Synergism
  • Fas Ligand Protein / physiology
  • Female
  • Humans
  • Leukemia, Mast-Cell / pathology*
  • Male
  • Mast Cells / drug effects*
  • Mast Cells / pathology
  • Mastocytosis, Systemic / pathology*
  • Methylation / drug effects
  • Middle Aged
  • Molecular Sequence Data
  • Neoplasm Proteins / metabolism
  • Point Mutation
  • Promoter Regions, Genetic / genetics
  • Protein Processing, Post-Translational / drug effects*
  • Proto-Oncogene Proteins c-kit / genetics
  • RNA, Small Interfering / pharmacology
  • fas Receptor / antagonists & inhibitors
  • fas Receptor / genetics
  • fas Receptor / metabolism*

Substances

  • Antimetabolites, Antineoplastic
  • DNA, Neoplasm
  • FAS protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • Neoplasm Proteins
  • RNA, Small Interfering
  • fas Receptor
  • Decitabine
  • Proto-Oncogene Proteins c-kit
  • Azacitidine