A small molecule Smac mimic potentiates TRAIL-mediated cell death of ovarian cancer cells

Gynecol Oncol. 2007 May;105(2):481-92. doi: 10.1016/j.ygyno.2007.01.011. Epub 2007 Feb 9.

Abstract

Objectives: Ovarian cancer remains a leading cause of death in women and development of new therapies is essential. Second mitochondria derived activator of caspase (Smac) has been described to sensitize for apoptosis. We have explored the proapoptotic activity of a small molecule mimic of Smac/DIABLO on ovarian cancer cell lines (A2780 cells and its chemoresistant derivatives A2780/ADR and A2780/DDP), cancer cell lines and in primary ovarian cancer cells.

Methods: The effects of a small molecule mimic of Smac/DIABLO on ovarian cancer cell lines and primary ovarian cancer cells were determined by cell proliferation, apoptosis and biochemical assays.

Results: This compound added alone elicited only a weak proapoptotic effect; however, it strongly synergizes with tumor necrosis factor-related apoptosis inducing ligand (TRAIL) or agonistic TRAILR2 antibody (Lexatumumab) in inducing apoptosis of ovarian cancer cells.

Conclusions: These observations suggest that small molecule mimic of Smac/DIABLO could be useful for the development of experimental strategies aiming to treat ovarian cancer. Interestingly, in addition to its well known proapoptotic effects, Smac/DIABLO elicited a significant increase of pro-caspase-3 levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Apoptosis / drug effects
  • Apoptosis Regulatory Proteins / metabolism
  • Biomimetic Materials / administration & dosage
  • Biomimetic Materials / pharmacology
  • Caspase 3 / metabolism
  • Caspase 9 / metabolism
  • Cell Growth Processes / drug effects
  • Cell Line, Tumor
  • Diynes / administration & dosage
  • Diynes / pharmacology*
  • Drug Synergism
  • Enzyme Activation / drug effects
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Mitochondrial Proteins
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / pathology
  • Peptide Fragments / administration & dosage
  • Peptide Fragments / pharmacology
  • Receptors, TNF-Related Apoptosis-Inducing Ligand / agonists
  • Receptors, Tumor Necrosis Factor / agonists
  • TNF-Related Apoptosis-Inducing Ligand / administration & dosage
  • TNF-Related Apoptosis-Inducing Ligand / pharmacology*
  • Tetrazoles / administration & dosage
  • Tetrazoles / pharmacology*
  • X-Linked Inhibitor of Apoptosis Protein / metabolism

Substances

  • 1,6-bis(4,7-diaza-6-methyl-5-oxo-3-((2-((5-(phenylthio)tetrazol-1-yl)methyl)pyrrolidin-1-yl)carbonyl)octyloxy)-2,4-hexadiyne
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Apoptosis Regulatory Proteins
  • DIABLO protein, human
  • Diynes
  • Intracellular Signaling Peptides and Proteins
  • Mitochondrial Proteins
  • Peptide Fragments
  • Receptors, TNF-Related Apoptosis-Inducing Ligand
  • Receptors, Tumor Necrosis Factor
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFRSF10A protein, human
  • TNFSF10 protein, human
  • Tetrazoles
  • X-Linked Inhibitor of Apoptosis Protein
  • XIAP protein, human
  • Caspase 3
  • Caspase 9
  • mapatumumab