17α-Methyl testosterone is a competitive inhibitor of aromatase activity in Jar choriocarcinoma cells and macrophage-like THP-1 cells in culture

被引:47
作者
Mor, G
Eliza, M
Song, J
Wiita, B
Chen, S
Naftolin, F
机构
[1] Yale Univ, Sch Med, Dept Obstet & Gynecol, Ctr Res Reprod Biol,FMB 335, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Reprod Neurosci Unit, FMB 335, New Haven, CT 06520 USA
[3] City Hope Natl Med Ctr, Beckman Res Inst, Duarte, CA 91010 USA
关键词
aromatase inhibitor; 17 alpha-methyl testosterone; methyl testosterone; androgen; hormone replacement therapy; breast; cancer;
D O I
10.1016/S0960-0760(01)00162-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
17alpha-Methyl testosterone is a synthetic androgen with affinity for the androgen receptor. 17alpha-Methyl testosterone is used widely as a component of hormone replacement therapy. Previous reports have indicated that contrary to testosterone, 17alpha-methyl testosterone is not aromatized. However, 17alpha-methyl testosterone still could affect local estrogen formation by regulating aromatase expression or by inhibiting aromatase action. Both possibilities have important clinical implications. To evaluate the effect of 17alpha-methyl testosterone on the expression and activity of aromatase, we tested the choriocarcinoma Jar cell line. a cell line that express high levels Of P-450 aromatase, and the macrophage-like THP-1 cells, which express aromatase only after undergoing differentiation, We found that in both cell lines, 17alpha-methyl testosterone inhibits aromatase activity in a dose-related manner. The curve of inhibition parallels that of letrozole and gives complete inhibition at 10(-4) M 17alpha-methyl testosterone, determined by the tritium release assay. 17alpha-Methyl testosterone does not have detectable effects on aromatase RNA and protein expression by Jar cells. Undifferentiated THP-1 cells had no aromatase activity and showed no effect of 17alpha-methyl testosterone, but differentiated THP-1 (macrophage-like) cells had a similar inhibition of aromatase activity by 17alpha-methyl testosterone to that seen in Jar cells. The Lineweaver-Burke plot shows 17alpha-methyl testosterone to be a competitive aromatase inhibitor. Our results show for the first time that 17alpha-methyl testosterone acts as an aromatase inhibitor. These findings are relevant for understanding the effects of 17alpha-methyl testosterone as a component of hormone replacement therapy. 17alpha-Methyl testosterone may, as a functional androgen and orally active steroidal inhibitor of endogenous estrogen production, also offer special possibilities for the prevention/treatment of hormone-sensitive cancers. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
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页码:239 / 246
页数:8
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