2-deprenyl-rheediaxanthone B isolated from Metaxya rostrata induces active cell death in colorectal tumor cells

PLoS One. 2013 Jun 11;8(6):e65745. doi: 10.1371/journal.pone.0065745. Print 2013.

Abstract

Metaxya rostrata C. Presl (Metaxyaceae) is a common tree fern in Central and South America that is used for the treatment of intestinal ulcers and tumours in ethnic medicine. Using a bioactivity-guided strategy 2-deprenyl-rheediaxanthone B (XB) has been isolated as one of the active principles in this plant. XB induced loss of cell viability in colorectal cancer cell lines at IC50 concentrations of 11-23 µM. This was caused by both accumulation of cells in the G2- and S-phase as well as by induction of active cell death in a time and concentration-dependent manner. Cells exposed to XB were incapable of undergoing regular mitosis due to down-regulation of FoxM1 and absence of chromosome condensation. The apoptosis-related proteins Bcl2 and Bclxl were up-regulated so that Caspase 3 was not activated and classical apoptosis was not observed. However, XB triggered damage pathways down-stream of ATR and activated Caspase 2 causing cell death by a mechanism similar to mitotic catastrophe. Our observations are the first to show the cytotoxic activity of 2-deprenyl-rheediaxanthone B and indicate that XB is an interesting new lead compound for cancer therapy that merits further development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Blotting, Western
  • Caco-2 Cells
  • Caspase 2 / metabolism
  • Cell Cycle / drug effects
  • Cell Line
  • Cell Survival / drug effects
  • Colorectal Neoplasms / metabolism
  • Ferns / chemistry*
  • HCT116 Cells
  • Humans
  • Inhibitory Concentration 50
  • Membrane Potential, Mitochondrial / drug effects
  • Plant Extracts / chemistry*
  • Plant Extracts / pharmacology*

Substances

  • Antineoplastic Agents
  • Plant Extracts
  • Caspase 2

Grants and funding

The study was suppported by the Austrian Science Foundation (P20354). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.