Halenaquinone inhibits RANKL-induced osteoclastogenesis

Bioorg Med Chem Lett. 2014 Nov 15;24(22):5315-7. doi: 10.1016/j.bmcl.2014.09.043. Epub 2014 Sep 23.

Abstract

Halenaquinone was isolated from the marine sponge Petrosia alfiani as an inhibitor of osteoclastogenic differentiation of murine RAW264 cells. It inhibited the RANKL (receptor activator of nuclear factor-κB ligand)-induced upregulation of TRAP (tartrate-resistant acid phosphatase) activity as well as the formation of multinuclear osteoclasts. In addition, halenaquinone substantially suppressed RANKL-induced IκB degradation and Akt phosphorylation. Thus, these results suggest that halenaquinone inhibits RANKL-induced osteoclastogenesis at least by suppressing the NF-κB and Akt signaling pathways.

Keywords: Halenaquinone; Marine sponge; Osteoclastogenesis; Petrosia alfiani.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cell Line
  • I-kappa B Proteins / metabolism
  • Mice
  • Osteoclasts / cytology
  • Osteoclasts / drug effects
  • Osteoclasts / metabolism
  • Osteogenesis / drug effects
  • Petrosia / chemistry
  • Petrosia / metabolism
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quinones / chemistry*
  • Quinones / isolation & purification
  • Quinones / pharmacology
  • RANK Ligand / toxicity
  • Signal Transduction / drug effects

Substances

  • I-kappa B Proteins
  • Quinones
  • RANK Ligand
  • halenaquinone
  • Proto-Oncogene Proteins c-akt