开发选择性类固醇激素受体调节剂有望成为未来防治骨质疏松药物的研究方向。

To develop a new selective steroid receptor modulator is one of the targets in future study to treat osteoporosis.

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大多数雄激素非依赖性前列腺癌均高表达AR和核受体辅活化子、如转录中间因子2（TIF-2），ARA24、PIAS、类固醇受体辅活化子-1（SRC-1）等有力地支持了这个假说。

The "superactive AR"hypothesis was supported by the fact that the majority of AIPC expresses high level of AR and nuclear receptor(NR) coactivators, such as TIF-2, ARA24, PIAS, SRC-1.

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