Abstract
Treatment with glucocorticoids is one of a limited number of options for androgen
independent prostate cancer. Neuroendocrine differentiation has been shown to contribute
to androgen-independent prostate cancer progression. To study the potential link between
neuroendocrine differentiation and the glucocorticoid action, we investigated the
effects of the product of neuroendocrine differentiation – bombesin on glucocorticoid
metabolizing enzymes – 11β-hydroxysteroid dehydrogenases in PC-3 cells. Our Western
analysis, RT-PCR, and activity assays demonstrate that while 18-hour exposure to bombesin
reduces 11β-hydroxy-steroid dehydrogenases-1 profiles (activities 25% less, protein
level 29% lower, mRNA levels 45% lower), contrarily it increases 11β-hydroxysteroid
dehydrogenases-2 profiles (activities 34%, protein levels 100%, mRNA levels 120%).
Blockade bombesin action with bombesin receptor antagonists and the enzyme degrading
bombesin prevented these changes, suggesting the observed modulations were bombesin
receptor-specific. In addition, bombesin increased the amounts of interleukin-8 and
mRNA of vascular endothelial growth factor receptor 2, which were lowered in the presence
of cortisol, suggesting that neuropeptide blockade may extend the benefits of glucocorticoids
in treating androgen-independent prostate cancer.
Key words
glucocorticoid - bombesin - 11β-hydroxysteroid dehydrogenases - neuroendocrine differentiation
- prostate cancer
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Correspondence
R. Shen
Weill Medical College of Cornell University
Dept of Urology
Rm F-902, Box 94
1300 York Ave
10021 New York
USA
Telefon: +1/212/746 50 28
Fax: +1/212/746 89 41
eMail: rshen@med.cornell.edu