Suberoylanilide hydroxamic acid (SAHA) overcomes multidrug resistance and induces cell death in P-glycoprotein-expressing cells

Int J Cancer. 2002 May 10;99(2):292-8. doi: 10.1002/ijc.10327.

Abstract

Multidrug resistance (MDR) mediated by the ATP-dependent efflux protein P-glycoprotein (P-gp) is a major obstacle to the successful treatment of many cancers. In addition to effluxing toxins, P-gp has been shown to protect tumor cells against caspase-dependent apoptosis mediated by Fas and tumor necrosis factor receptor (TNFR) ligation, serum starvation and ultraviolet (UV) irradiation. However, P-gp does not protect against caspase-independent cell death mediated by granzyme B or pore-forming proteins (perforin, pneumolysin and activated complement). We examined the effects of the chemotherapeutic hybrid polar compound suberoylanilide hydroxamic acid (SAHA) on P-gp-expressing MDR human tumor cell lines. In the CEM T-cell line, SAHA, a histone deacetylase inhibitor, induced equivalent death in P-gp-positive cells compared with P-gp-negative cells. Cell death was marked by the caspase-independent release of cytochrome c, reactive oxygen species (ROS) production and Bid cleavage that was not affected by P-gp expression. However, consistent with our previous findings, SAHA-induced caspase activation was inhibited in P-gp-expressing cells. These data provide evidence that P-gp inhibits caspase activation after chemotherapeutic drug treatment and demonstrates that SAHA may be of value for the treatment of P-gp-expressing MDR cancers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / analysis*
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Caspase 3
  • Caspases / metabolism
  • Cell Cycle / drug effects
  • Cell Death / drug effects*
  • Chromium Radioisotopes / metabolism
  • Colonic Neoplasms / chemistry
  • Colonic Neoplasms / pathology
  • Cytochrome c Group / metabolism
  • Drug Resistance, Multiple*
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • Gene Expression
  • Histone Deacetylase Inhibitors
  • Histones / metabolism
  • Humans
  • Hydroxamic Acids / pharmacology*
  • Leukemia, Erythroblastic, Acute / metabolism
  • Leukemia, Erythroblastic, Acute / pathology
  • Leukemia, T-Cell / metabolism
  • Leukemia, T-Cell / pathology
  • Poly(ADP-ribose) Polymerases / metabolism
  • Reactive Oxygen Species / metabolism
  • Tumor Cells, Cultured
  • Vincristine / pharmacology
  • Vorinostat

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antineoplastic Agents
  • Chromium Radioisotopes
  • Cytochrome c Group
  • Enzyme Inhibitors
  • Histone Deacetylase Inhibitors
  • Histones
  • Hydroxamic Acids
  • Reactive Oxygen Species
  • Vorinostat
  • Vincristine
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • Caspase 3
  • Caspases