Abstract
One novel strategy for the blockade of the androgen receptor could be the selective
inhibition of androgen receptor by antisense oligonucleotides or small interfering
RNA molecules. Here we describe the down regulation of the androgen receptor in cultured
human SZ95 sebocytes with antisense oligonucleotides modified with phosphorothioates
and 2′-O -methylribosyl residues. The ability of antisense oligonucleotides to cross the cellular
membrane was enhanced by establishing a transient transfection system based on cationic
lipid vesicles. Both antisense oligonucleotide types administered caused assumedly
translational arrest. Dose-dependent inhibition of androgen receptor protein expression
was observed after SZ95 sebocyte transfection with modified phosphorothioate oligonucleotides
and modified 2′-O -methylribonucleotides which were directed against the translational start of the
androgen receptor mRNA. The strongest transient inhibition of androgen receptor expression
was detected after 14 hours with 1.0 μM antisense 2′-O -methylribonucleotides (88±1.3%, p<0.001). With longer recovery times than 24 hours,
androgen receptor protein expression returned to the native control levels. Inhibition
of the expression of androgen receptor by antisense oligonucleotides, reduced the
enhanced proliferation of SZ95 sebocytes challenged by testosterone and 5α-dihydrotestosterone.
This administration opens new therapeutic possibilities in androgen-associated skin
diseases, since we could also show androgen inhibition with these antisense oligonucleotides
in a reconstituted human epidermis model (Horm Metab Res 2007; 39:157-165).
Keywords
androgens - sebaceous glands - transient transfection - biological activity
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Correspondence
C. C.Zouboulis
Departments of Dermatology and Immunology
Dessau Medical Center
Auenweg 38
06847 Dessau
Germany
Telefon: +49/340/501 40 00
Fax: +49/340/501 40 25
eMail: christos.zouboulis@klinikum-dessau.de