Brassinin and its derivatives as potential anticancer agents

Toxicol In Vitro. 2014 Aug;28(5):909-15. doi: 10.1016/j.tiv.2014.04.002. Epub 2014 Apr 18.

Abstract

The aim of the study was to investigate the anti-proliferative activity of brassinin and its derivatives on human cancer cell lines. We found that among twenty-one tested compounds, 1- methoxybrassinin exerted the most potent anti-proliferative activity in Caco-2 cells with IC₅₀ 8.2 (±1.2)μmoll(-1). The flow cytometric analysis revealed a 1-methoxybrassinin-induced increase in the sub-G1 DNA content fraction which is considered to be a marker of apoptotic cell death. Apoptosis was also confirmed by DNA fragmentation assay. Moreover, quantitative real-time PCR showed that 1-methoxybrassinin upregulated the expression of pro-apoptotic Bax and downregulated the expression of anti-apoptotic genes Bcl-2 and Bcl-xL. The compound also increased activity of caspase-3, -7, cleaved PARP and decreased intracellular GSH content. The present study has assessed the in vitro anti-proliferative potential of 1-methoxybrassinin. The results generate a rationale for in vivo efficacy studies with this compound in preclinical cancer models.

Keywords: Anti-proliferative effect; Apoptosis; Brassinin; Indole phytoalexins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Caco-2 Cells
  • Caspase 3 / metabolism
  • Caspase 7 / metabolism
  • Cell Cycle / drug effects
  • Cell Survival / drug effects
  • Glutathione / metabolism
  • HCT116 Cells
  • Hep G2 Cells
  • Humans
  • Indoles / pharmacology*
  • Poly(ADP-ribose) Polymerases / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Thiocarbamates / pharmacology*

Substances

  • Antineoplastic Agents
  • Indoles
  • Proto-Oncogene Proteins c-bcl-2
  • Thiocarbamates
  • brassinin
  • Poly(ADP-ribose) Polymerases
  • Caspase 3
  • Caspase 7
  • Glutathione