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Alpha-keto acid metabolites of naturally occurring organoselenium compounds as inhibitors of histone deacetylase in human prostate cancer cells.

Histone deacetylase (HDAC) inhibitors are gaining interest as cancer therapeutic agents. We tested the hypothesis that natural organoselenium compounds might be metabolized to HDAC inhibitors in human prostate cancer cells. Se-Methyl-L-selenocysteine (MSC) and selenomethionine are amino acid components of selenium-enriched yeast. In a cell-free system, glutamine transaminase K (GTK) and L-amino acid oxidase convert MSC to the corresponding alpha-keto acid, beta-methylselenopyruvate (MSP), and L-amino acid oxidase converts selenomethionine to its corresponding alpha-keto acid, alpha-keto-gamma-methylselenobutyrate (KMSB). Although methionine (sulfur analogue of selenomethionine) is an excellent substrate for GTK, selenomethionine is poorly metabolized. Structurally, MSP and KMSB resemble the known HDAC inhibitor butyrate. We examined androgen-responsive LNCaP cells and androgen-independent LNCaP C4-2, PC-3, and DU145 cells and found that these human prostate cancer cells exhibit endogenous GTK activities. In the corresponding cytosolic extracts, the metabolism of MSC was accompanied by the concomitant formation of MSP. In MSP-treated and KMSB-treated prostate cancer cell lines, acetylated histone 3 levels increased within 5 hours, and returned to essentially baseline levels by 24 hours, suggesting a rapid, transient induction of histone acetylation. In an in vitro HDAC activity assay, the selenoamino acids, MSC and selenomethionine, had no effect at concentrations up to 2.5 mmol/L, whereas MSP and KMSB both inhibited HDAC activity. We conclude that, in addition to targeting redox-sensitive signaling proteins and transcription factors, alpha-keto acid metabolites of MSC and selenomethionine can alter HDAC activity and histone acetylation status. These findings provide a potential new paradigm by which naturally occurring organoselenium might prevent the progression of human prostate cancer.

Pubmed ID: 19584079


  • Lee JI
  • Nian H
  • Cooper AJ
  • Sinha R
  • Dai J
  • Bisson WH
  • Dashwood RH
  • Pinto JT


Cancer prevention research (Philadelphia, Pa.)

Publication Data

July 8, 2009

Associated Grants

  • Agency: NCI NIH HHS, Id: CA090890
  • Agency: NCI NIH HHS, Id: CA111842
  • Agency: NCI NIH HHS, Id: CA122959
  • Agency: NIEHS NIH HHS, Id: ES8421
  • Agency: NCI NIH HHS, Id: P01 CA090890
  • Agency: NCI NIH HHS, Id: P01 CA090890-01A20003
  • Agency: NCI NIH HHS, Id: P01 CA090890-01A29001
  • Agency: NCI NIH HHS, Id: R01 CA111842-01A2
  • Agency: NCI NIH HHS, Id: R01 CA111842-03
  • Agency: NCI NIH HHS, Id: R01 CA122959
  • Agency: NCI NIH HHS, Id: R01 CA122959-02
  • Agency: NIEHS NIH HHS, Id: R01 ES008421-11

Mesh Terms

  • Cell Line, Tumor
  • Chromatography, High Pressure Liquid
  • Histone Deacetylase Inhibitors
  • Histones
  • Humans
  • Inhibitory Concentration 50
  • Keto Acids
  • L-Amino Acid Oxidase
  • Lyases
  • Male
  • Mass Spectrometry
  • Methionine
  • Prostatic Neoplasms
  • Protein Processing, Post-Translational
  • Selenium
  • Transaminases