Planta Med 2004; 70(5): 397-400
DOI: 10.1055/s-2004-818965
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Silibinin Down-Regulates Prostate Epithelium-Derived Ets Transcription Factor in LNCaP Prostate Cancer Cells

Paul Thelen1 , Hubertus Jarry2 , Rolf-Hermann Ringert1 , Wolfgang Wuttke2
  • 1Department of Urology, Georg-August-University, Göttingen, Germany
  • 2Department of Clinical and Experimental Endocrinology, Georg-August-University, Göttingen, Germany
This study was supported by the European Union: (E)UROESTROGEN(E)S contract QLK6-CT-200-00 656
Weitere Informationen

Publikationsverlauf

Received: September 22, 2003

Accepted: January 30, 2004

Publikationsdatum:
04. Mai 2004 (online)

Abstract

The androgen-sensitive human prostate cancer cell line LNCaP expresses the estrogen receptor β and androgen receptor and can be stimulated by androgens to secrete prostate-specific antigen (PSA). In this study we demonstrate the cancer protective potential of silibinin, a flavolignan derived from the fruits of Silybum marianum, which down-regulates the co-activator of the androgen receptor, the prostate epithelium-derived Ets transcription factor (PDEF) and consequently the secretion of PSA. LNCaP cells were treated with various concentrations of silibinin in the presence or in the absence of 5α-dihydrotestosterone (DHT). We used real-time RT-PCR to quantify mRNA expression of PDEF and PSA with gene-specific dual-labelled fluorescence probes. PSA secretion from LNCaP cells in conditioned media was measured with the Elecsys® System 2010. Silibinin down-regulated PSA mRNA expression and PSA secretion in conditioned medium under basal and DHT (10 - 8 M) stimulated conditions, which was paralleled by PDEF down-regulation. DHT alone stimulated PDEF and PSA gene expression and PSA secretion. The down-regulation of basal as well as DHT stimulated PDEF and PSA by silibinin demonstrates the antiproliferative potential of this agent. These effects underline the possible therapeutic use of silibinin in the management of prostate cancer.

Abbreviations

Ets:E twenty-six transcription factor

PDEF:prostate epithelium-derived Ets factor

DHT:5α-dihydrotestosterone

PSA:prostate-specific antigen

IGFBP-3:insulin-like growth factor-binding protein 3

ER:estrogen receptor

cRNA:complementary RNA

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Dr. Paul Thelen

Abt. Urologie

Georg-August-Universität

Robert Koch-Str. 40

37075 Göttingen

Germany

Telefon: +49-551-398-651

Fax: +49-551-396-165

eMail: pthelen@gwdg.de