Laboratories for Reproductive Biology, Department of Pediatrics, University of North Carolina, Chapel Hill, NC 27599-7500, USA.
J Biol Chem. 2013 Jan 18;288(3):1939-52. doi: 10.1074/jbc.M112.428409. Epub 2012 Nov 21.
Prostate cancer growth and progression depend on androgen receptor (AR) signaling through transcriptional mechanisms that require interactions with coregulatory proteins, one of which is the primate-specific steroid receptor coregulator melanoma antigen-A11 (MAGE-A11). In this report, we provide evidence how increased expression of MAGE-A11 during prostate cancer progression enhances AR signaling and prostate cancer growth. MAGE-A11 protein levels were highest in castration-recurrent prostate cancer. The cyclic AMP-induced increase in androgen-dependent and androgen-independent AR transcriptional activity correlated with an increase in MAGE-A11 and was inhibited by silencing MAGE-A11 expression. MAGE-A11 mediated synergistic AR transcriptional activity in LAPC-4 prostate cancer cells. The ability of MAGE-A11 to rescue transcriptional activity of complementary inactive AR mutants and promote coimmunoprecipitation between unlike forms of AR suggests that MAGE-A11 links transcriptionally active AR dimers. A model for the AR·MAGE-A11 multidimeric complex is proposed in which one AR FXXLF motif of the AR dimer engages in the androgen-dependent AR NH(2)- and carboxyl-terminal interaction, whereas the second FXXLF motif region of the AR dimer interacts with dimeric MAGE-A11. The AR·MAGE-A11 multidimeric complex accounts for the dual functions of the AR FXXLF motif in the androgen-dependent AR NH(2)- and carboxyl-terminal interaction and binding MAGE-A11 and for synergy between reported AR splice variants and full-length AR. We conclude that the increased expression of MAGE-A11 in castration-recurrent prostate cancer, which is enhanced by cyclic AMP signaling, increases AR-dependent growth of prostate cancer by MAGE-A11 forming a molecular bridge between transcriptionally active AR dimers.
前列腺癌的生长和进展依赖于雄激素受体 (AR) 信号转导,该信号转导通过转录机制实现,需要与共调节蛋白相互作用,其中之一是灵长类特异性类固醇受体共调节蛋白黑色素瘤抗原-A11 (MAGE-A11)。在本报告中,我们提供了证据表明,前列腺癌进展过程中 MAGE-A11 的表达增加增强了 AR 信号转导和前列腺癌的生长。在去势复发的前列腺癌中,MAGE-A11 蛋白水平最高。环磷酸腺苷诱导的雄激素依赖性和非依赖性 AR 转录活性的增加与 MAGE-A11 的增加相关,并被沉默 MAGE-A11 表达所抑制。MAGE-A11 在 LAPC-4 前列腺癌细胞中介导协同的 AR 转录活性。MAGE-A11 能够拯救互补失活的 AR 突变体的转录活性并促进不同形式的 AR 之间的共免疫沉淀的能力表明,MAGE-A11 将转录活性的 AR 二聚体连接在一起。提出了一个 AR·MAGE-A11 多二聚体复合物模型,其中 AR 二聚体的一个 AR FXXLF 基序参与雄激素依赖性的 AR NH2-和羧基末端相互作用,而 AR 二聚体的第二个 FXXLF 基序区域与二聚体 MAGE-A11 相互作用。AR·MAGE-A11 多二聚体复合物解释了 AR FXXLF 基序在雄激素依赖性的 AR NH2-和羧基末端相互作用以及结合 MAGE-A11 中的双重功能,以及报道的 AR 剪接变体和全长 AR 之间的协同作用。我们得出结论,去势复发的前列腺癌中 MAGE-A11 的表达增加,这是由环磷酸腺苷信号增强的,通过在转录活性的 AR 二聚体之间形成分子桥,增加了 MAGE-A11 形成的 AR 依赖性前列腺癌细胞的生长。