Negative regulation of parathyroid hormone-related protein expression by steroid hormones

• Published in: Biochemical and biophysical research communications 2011-04, Vol.407 (3), p.472-478
• Main Authors: Kajitani, Takashi, Tamamori-Adachi, Mimi, Okinaga, Hiroko, Chikamori, Minoru, Iizuka, Masayoshi, Okazaki, Tomoki
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; ANDROGENS; Cell Line; Cell Line, Tumor; DEXAMETHASONE; Down-Regulation; ESTRADIOL; GROWTH FACTORS; Hormones - pharmacology; Hormones - physiology; Humans; INHIBITION; NEOPLASMS; Nuclear receptors; Parathyroid hormone-related protein; Parathyroid Hormone-Related Protein - antagonists & inhibitors; Parathyroid Hormone-Related Protein - biosynthesis; Parathyroid Hormone-Related Protein - genetics; PHOSPHATES; PROGESTERONE; Protein Biosynthesis - drug effects; Protein Biosynthesis - genetics; Protein Biosynthesis - physiology; RECEPTORS; RETINOIC ACID; RNA; Steroid hormones; Steroids - pharmacology; Steroids - physiology; Transcription
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2011.03.037

► Steroid hormones repress expression of PTHrP in the cell lines where the corresponding nuclear receptors are expressed. ► Nuclear receptors are required for suppression of PTHrP expression by steroid hormones, except for androgen receptor. ► Androgen-induced suppression of PTHrP expression appears to be mediated by estrogen receptor. Elevated parathyroid hormone-related protein (PTHrP) is responsible for humoral hypercalcemia of malignancy (HHM), which is of clinical significance in treatment of terminal patients with malignancies. Steroid hormones were known to cause suppression of PTHrP expression. However, detailed studies linking multiple steroid hormones to PTHrP expression are lacking. Here we studied PTHrP expression in response to steroid hormones in four cell lines with excessive PTHrP production. Our study established that steroid hormones negatively regulate PTHrP expression. Vitamin D receptor, estrogen receptor α, glucocorticoid receptor, and progesterone receptor, were required for repression of PTHrP expression by the cognate ligands. A notable exception was the androgen receptor, which was dispensable for suppression of PTHrP expression in androgen-treated cells. We propose a pathway(s) involving nuclear receptors to suppress PTHrP expression.