Orphan receptors COUP-TF and DAX-1 as targets in disordered CYP17 expression in adrenocortical tumors

被引:13
作者
Shibata, H [1 ]
Ikeda, Y
Morohashi, K
Mukai, T
Kurihara, I
Ando, T
Suzuki, T
Kobayashi, S
Hayashi, K
Hayashi, M
Saito, I
Saruta, T
机构
[1] Keio Univ, Sch Med, Ctr Hlth, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Internal Med, Tokyo 1608582, Japan
[3] Univ Tsukuba, Inst Basic Med Sci, Dept Anat, Tsukuba, Ibaraki 3058575, Japan
[4] Natl Inst Basic Biol, Dept Dev Biol, Okazaki, Aichi 4448585, Japan
关键词
D O I
10.3109/07435800009048636
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CYP17 gene transcription is activated by SF-1 binding to a cyclic AMP-responsive sequence within the promoter region of the gene, and its transcription is inhibited by COUP-TF binding to the sequence. Another orphan receptor, DAX-1, is shown to act as a suppressor of SF-1-mediated transcription We examined the expression level of these orphan receptors in adrenocortical tumors and compared the results with CYP17 expression. CYP17 was highly expressed in cortisol-producing adenomas, whereas COUP-TF and DAX-1 expression levels were very low. In deoxycorticosterone-producing adenomas, on the other hand, CYP17 expression was extremely low, whereas DAX-1 was highly expressed and SF-1 expression was slightly decreased. In conclusion, the reciprocal expression of CYP17 and the transcriptional repressors COUP-TF and DAX-1 indicates that these orphan receptors have a pathophysiologic role in the excessive hormone production in cortisol- and deoxycorticosterone-producing adrenocortical tumors.
引用
收藏
页码:1039 / 1044
页数:6
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