Wang Hongbo, Sun Daqian, Ji Peng, Mohler James, Zhu Liang
Department of Developmental and Molecular Biology, The Albert Einstein Comprehensive Cancer Center and Liver Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
J Cell Sci. 2008 Aug 1;121(Pt 15):2578-87. doi: 10.1242/jcs.030742. Epub 2008 Jul 15.
Androgen-androgen-receptor (androgen-AR) signaling in normal prostate epithelium promotes terminal luminal epithelial cell differentiation. In androgen-dependent prostate-cancer cells, androgen-AR signaling gains the ability to promote both differentiation and proliferation. How this signaling promotes proliferation of androgen-dependent prostate-cancer cells and its relationship with the differentiation-promoting functions of the AR are important issues regarding the biology of androgen-dependent prostate-cancer cells. Herein, we report the identification of an AR-Skp2 pathway in prostate-cancer cells that depend on the AR for proliferation; in this pathway, AR is a robust upstream regulator of Skp2 through blocking the D-box-dependent degradation of this protein, and Skp2, in turn, serves as an essential downstream effector of AR in promoting proliferation independently of the differentiation-promoting function of AR. These results provide new knowledge on how AR functions in androgen-dependent prostate-cancer cells and identify strategies to specifically target the proliferation-promoting function of AR without compromising cancer-cell differentiation.
正常前列腺上皮中的雄激素-雄激素受体(androgen-AR)信号传导促进终末腔上皮细胞分化。在雄激素依赖性前列腺癌细胞中,雄激素-AR信号传导获得了促进分化和增殖的能力。这种信号传导如何促进雄激素依赖性前列腺癌细胞的增殖以及它与AR促进分化功能的关系,是有关雄激素依赖性前列腺癌细胞生物学的重要问题。在此,我们报告在依赖AR进行增殖的前列腺癌细胞中鉴定出一条AR-Skp2信号通路;在该通路中,AR通过阻断该蛋白依赖D-box的降解,成为Skp2强大的上游调节因子,而Skp2反过来作为AR在促进增殖方面的重要下游效应器,独立于AR促进分化的功能。这些结果为AR在雄激素依赖性前列腺癌细胞中的作用方式提供了新知识,并确定了在不损害癌细胞分化的情况下特异性靶向AR促进增殖功能的策略。