Studies on the inhibition of tumor cell growth and microtubule assembly by 3-hydroxy-4-[(E)-(2-furyl)methylidene]methyl-3-cyclopentene-1,2-dione, an intensively coloured Maillard reaction product

Food Chem Toxicol. 2002 Jan;40(1):9-18. doi: 10.1016/s0278-6915(01)00093-x.

Abstract

Very recently, 3-hydroxy-4-[(E)-(2-furyl)methylidene]methyl-3-cyclopentene-1,2-dione (1) has been successfully identified as an intensively coloured Maillard product formed from glucose and L-proline upon thermal food processing. Using a biomimetic synthetic strategy, reference material of compound 1 was prepared and purified, and then used to study its effect on the growth of human tumor cells. Compound 1 was found to potently inhibit the growth of human tumor cells in vitro. Using a reporter gene assay we could show that in growth inhibitory concentrations compound 1 effectively inhibits the phosphorylation of the transcription factor Elk-1. In addition, 1 was found to affect the microtubule skeleton. The human mammary carcinoma cell line MCF-7 exhibits a decrease of the microtubule organisation when treated for 24 h with 1 (> or =20 microM). At concentrations of 30 microM and above a loss of microtubule integrity is observed after 1 h incubation. In vitro studies demonstrated that the polymerisation and, to a minor extent, also the depolymerisation of tubulin, isolated and purified from bovine brain, is inhibited in a dose-dependent manner at concentrations of 30 microM and above. This is the first time that a non-enzymatically formed browning compound of known structure was reported to effectively inhibit tumor cell growth and microtubule assembly.

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / pharmacology*
  • Brain Chemistry
  • Breast Neoplasms / pathology
  • Cattle
  • Cell Cycle / drug effects
  • Cell Division / drug effects*
  • Cyclopentanes / administration & dosage
  • Cyclopentanes / chemical synthesis
  • Cyclopentanes / pharmacology*
  • DNA Damage
  • DNA-Binding Proteins*
  • Dose-Response Relationship, Drug
  • Female
  • Furans / administration & dosage
  • Furans / chemical synthesis
  • Furans / pharmacology*
  • Humans
  • Maillard Reaction*
  • Microtubules / drug effects*
  • Microtubules / ultrastructure
  • Neoplasms / pathology*
  • Phosphorylation
  • Polymers / metabolism
  • Proto-Oncogene Proteins / metabolism
  • Transcription Factors*
  • Tubulin / metabolism
  • Tumor Cells, Cultured
  • ets-Domain Protein Elk-1

Substances

  • 3-hydroxy-4-(-(2-furyl)methylidene)methyl-3-cyclopentene-1,2-dione
  • Antineoplastic Agents
  • Cyclopentanes
  • DNA-Binding Proteins
  • ELK1 protein, human
  • Furans
  • Polymers
  • Proto-Oncogene Proteins
  • Transcription Factors
  • Tubulin
  • ets-Domain Protein Elk-1