Two natural products, trans-phytol and (22E)-ergosta-6,9,22-triene-3β,5α,8α-triol, inhibit the biosynthesis of estrogen in human ovarian granulosa cells by aromatase (CYP19)

• Published in: Toxicology and applied pharmacology 2014-08, Vol.279 (1), p.23-32
• Main Authors: Guo, Jiajia, Yuan, Yun, Lu, Danfeng, Du, Baowen, Xiong, Liang, Shi, Jiangong, Yang, Lijuan, Liu, Wanli, Yuan, Xiaohong, Zhang, Guolin, Wang, Fei
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; Aromatase; Aromatase - metabolism; Aromatase Inhibitors - pharmacology; Biological and medical sciences; Biological Products - pharmacology; BIOSYNTHESIS; Blotting, Western; Cell Proliferation - drug effects; Cell Survival - drug effects; Cells, Cultured; Cholesterol - analogs & derivatives; Cholesterol - pharmacology; Cyclic AMP - metabolism; Diterpenes - pharmacology; DRUGS; ENZYME IMMUNOASSAY; Ergosta-6,9,22-triene-3β,5α,8α-triol; Estrogen Antagonists - pharmacology; Estrogen biosynthesis; ESTROGENS; Estrogens - biosynthesis; Female; FSH; Granulosa cells; Granulosa Cells - drug effects; Granulosa Cells - metabolism; Humans; INHIBITION; MAMMARY GLANDS; MAP Kinase Signaling System - drug effects; Medical sciences; Medicine, Chinese Traditional; MESSENGER-RNA; NEOPLASMS; OVARIES; Ovary - drug effects; Ovary - metabolism; p38 MAPK; PHOSPHORYLATION; Phytol; Poaceae - chemistry; PROSTAGLANDINS; Protein Kinases - metabolism; Real-Time Polymerase Chain Reaction; Recombinant Proteins - metabolism; Signal Transduction - drug effects; Toxicology; TRANSCRIPTION; Transfection
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2014.05.008

Aromatase is the only enzyme in vertebrates to catalyze the biosynthesis of estrogens. Although inhibitors of aromatase have been developed for the treatment of estrogen-dependent breast cancer, the whole-body inhibition of aromatase causes severe adverse effects. Thus, tissue-selective aromatase inhibitors are important for the treatment of estrogen-dependent cancers. In this study, 63 natural products with diverse structures were examined for their effects on estrogen biosynthesis in human ovarian granulosa-like KGN cells. Two compounds—trans-phytol (SA-20) and (22E)-ergosta-6,9,22-triene-3β,5α,8α-triol (SA-48)—were found to potently inhibit estrogen biosynthesis (IC50: 1μM and 0.5μM, respectively). Both compounds decreased aromatase mRNA and protein expression levels in KGN cells, but had no effect on the aromatase catalytic activity in aromatase-overexpressing HEK293A cells and recombinant expressed aromatase. The two compounds decreased the expression of aromatase promoter I.3/II. Neither compound affected intracellular cyclic AMP (cAMP) levels, but they inhibited the phosphorylation or protein expression of cAMP response element-binding protein (CREB). The effects of these two compounds on extracellular regulated kinase (ERK), c-Jun N-terminal kinase (JNK), p38 mitogen-activated protein kinases (MAPKs), and AKT/phosphoinositide 3-kinase (PI3K) pathway were examined. Inhibition of p38 MAPK could be the mechanism underpinning the actions of these compounds. Our results suggests that natural products structurally similar to SA-20 and SA-48 may be a new source of tissue-selective aromatase modulators, and that p38 MAPK is important in the basal control of aromatase in ovarian granulosa cells. SA-20 and SA-48 warrant further investigation as new pharmaceutical tools for the prevention and treatment of estrogen-dependent cancers. •Two natural products inhibited estrogen biosynthesis in human ovarian granulosa cells.•They inhibited aromatase transcription without affecting its catalytic activity.•They decreased the transcription or protein expression of CREB.•They inhibited p38 MAPK to exert their inhibitory effects on aromatase expression.