Apoptosis in MCF-7 breast cancer cells induced by S-alkenylmercaptocysteine (CySSR) species derived from Allium tissues in combination with sodium selenite

Food Chem Toxicol. 2014 Jun:68:1-10. doi: 10.1016/j.fct.2014.03.002. Epub 2014 Mar 12.

Abstract

S-Allylmercaptocysteine (CySSA) from garlic is known to exhibit anti-cancer effects. Apoptosis induction by CySSA was contrasted with S-1-propenylmercaptocysteine (CySSPe) (the major onion analog) in the presence of Na2SeO3 (Se) in breast cancer cells MCF-7. The dose of CySSA or CySSPe alone required to reduce viable cells by 50% was >400μM, and this was reduced to 62μM and 91μM for CySSA+Se and CySSPe+Se, respectively, at molar ratios of 39:1. Synergism of the mixtures was confirmed by isobologram analysis and the treatments evoked enhanced thiol efflux from MCF-7 cells. Apoptosis was confirmed by Annexin-V and propidium iodide staining. Cell cycle arrest occurred at the G2/M and sub-G1 interphases. Both CySSR+Se mixtures reduced the levels of Akt. CySSPe+Se elevated GSK-3 protein levels, whereas CySSA+Se did not. CySSR+Se mixtures enhanced phospho-c-Jun levels, with CySSA+Se more potent than CySSPe+Se. Corresponding increases in phospho-p53, Bax and Bad levels were observed, indicating apoptosis occurred via the mitochondrial pathway. Lack of caspases 6/7 activation implicated a caspase-independent pathway for apoptosis. Reduction of imported CySSR and export of thiols by MCF-7 cells facilitates the reduction of selenite to yield H2Se, a cytotoxic agent. This appears to be the first report of an anti-cancer effect of CySSPe.

Keywords: Allium; Apoptosis; S-alkenylmercaptocysteine; Sodium selenite; Synergism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allium / chemistry*
  • Annexin A5 / metabolism
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects*
  • Caspase 6 / genetics
  • Caspase 6 / metabolism
  • Caspase 7 / genetics
  • Caspase 7 / metabolism
  • Cell Cycle Checkpoints / drug effects
  • Cell Survival / drug effects
  • Cysteine / analogs & derivatives*
  • Cysteine / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Female
  • Glycogen Synthase Kinase 3 / metabolism
  • Humans
  • MCF-7 Cells
  • Mitochondria / drug effects
  • Plant Extracts / pharmacology*
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction
  • Sodium Selenite / pharmacology*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism
  • bcl-2-Associated X Protein / genetics
  • bcl-2-Associated X Protein / metabolism
  • bcl-Associated Death Protein / genetics
  • bcl-Associated Death Protein / metabolism

Substances

  • Annexin A5
  • Antineoplastic Agents
  • BAD protein, human
  • BAX protein, human
  • Plant Extracts
  • S-allylmercaptocysteine
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • bcl-Associated Death Protein
  • Proto-Oncogene Proteins c-akt
  • Glycogen Synthase Kinase 3
  • CASP6 protein, human
  • CASP7 protein, human
  • Caspase 6
  • Caspase 7
  • Sodium Selenite
  • Cysteine