Geraniol inhibits prostate cancer growth by targeting cell cycle and apoptosis pathways

Biochem Biophys Res Commun. 2011 Apr 1;407(1):129-34. doi: 10.1016/j.bbrc.2011.02.124. Epub 2011 Mar 1.

Abstract

The progression of prostate cancer is associated with escape from cell cycle arrest and apoptosis under androgen-depleted conditions. Here, we found that geraniol, a naturally occurring monoterpene, induces cell cycle arrest and apoptosis in cultured cells and tumor grafted mice using PC-3 prostate cancer cells. Geraniol modulated the expression of various cell cycle regulators and Bcl-2 family proteins in PC-3 cells in vitro and in vivo. Furthermore, we showed that the combination of sub-optimal doses of geraniol and docetaxel noticeably suppresses prostate cancer growth in cultured cells and tumor xenograft mice. Therefore, our findings provide insight into unraveling the mechanisms underlying escape from cell cycle arrest and apoptosis and developing therapeutic strategies against prostate cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyclic Monoterpenes
  • Animals
  • Apoptosis / drug effects*
  • Cell Cycle / drug effects*
  • Cell Proliferation / drug effects*
  • Drug Resistance, Neoplasm / drug effects*
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Prostatic Neoplasms / drug therapy*
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • TRPM Cation Channels / metabolism
  • Terpenes / pharmacology*
  • Terpenes / therapeutic use
  • Xenograft Model Antitumor Assays

Substances

  • Acyclic Monoterpenes
  • Proto-Oncogene Proteins c-bcl-2
  • TRPM Cation Channels
  • TRPM8 protein, human
  • Terpenes
  • geraniol