Anti-androgen effects of extracts and compounds from Ganoderma lucidum

Chem Biodivers. 2009 Feb;6(2):231-43. doi: 10.1002/cbdv.200800019.

Abstract

The 30% EtOH extracts of Ganoderma lucidum Fr. Karst (Ganodermateceae) showed weak 5alpha-reductase inhibitory activity and binding ability to androgen receptor. When LNCaP (lymph-node carcinoma of the prostate) cells were treated with the EtOH extracts, cell proliferation was inhibited. Treatment with the extracts significantly inhibited the testosterone-induced growth of the ventral prostate in castrated rats. These results showed that G. lucidum might be a useful ingredient in the treatment of androgen-induced diseases, such as benign prostatic hyperplasia or prostate cancer. From the 30% EtOH extracts, we isolated ganoderiol F, which showed binding activity to androgen receptor and inhibited LNCaP cell proliferation, as one of the active compounds in the 30% EtOH extracts.

MeSH terms

  • Androgen Antagonists / chemistry
  • Androgen Antagonists / pharmacology*
  • Animals
  • Cell Line, Tumor
  • Humans
  • Male
  • Organic Chemicals / chemistry
  • Organic Chemicals / pharmacology
  • Rats
  • Reishi / chemistry*
  • Triterpenes / isolation & purification
  • Triterpenes / pharmacology

Substances

  • Androgen Antagonists
  • Organic Chemicals
  • Triterpenes
  • ganoderiol F