Laboratory of Experimental Endocrinology, University of Crete, School of Medicine, P.O. Box 2208, Heraklion GR-71003, Greece.
Mol Oncol. 2010 Apr;4(2):135-49. doi: 10.1016/j.molonc.2010.01.004. Epub 2010 Feb 2.
Membrane-initiated androgen actions have now been acknowledged, even though a specific binding site has not been biochemically characterized yet. Recent data indicate that testosterone-BSA, a non-permeable testosterone analog, can exert specific actions in breast cancer cell lines, including proper transcriptional effects, independent of the intracellular androgen sites. In the present work we explore the effects of testosterone-BSA in two specifically modified pathways, revealed by early trascriptome analysis, namely the non-genotropic androgen signaling and the HIF1alpha pathway. We provide evidence that p38 MAPK and PI3K/Akt/NFkappaB and/or Rho/Actin pathways are directly involved in testosterone-induced apoptosis, while the JNK/c-JUN pathway is involved in membrane site-initiated transcription. Furthermore we show that membrane-acting androgens modify the transcription of the erythropoietin receptor (EPOR), leading to erythropoietin-initiated actions. Interestingly, association of recombinant human erythropoietin (rHuEPO) together with testosterone-BSA protects cells from apoptosis, through discrete signaling events. The effect of testosterone-BSA is exerted through the classical erythropoietin promoter, while rHuEPO decreases the transcription of EPOR acting on a newly identified regulatory/promoter region, upstream of its known promoter. These results suggest a new interaction of membrane-acting androgen with EPOR and should be taken into account in the pharmaceutical manipulations of breast cancer patients.
现在已经承认了膜介导的雄激素作用,尽管尚未在生化上表征出特定的结合位点。最近的数据表明,非通透性的睾酮类似物睾酮-BSA 可以在乳腺癌细胞系中发挥特定的作用,包括适当的转录效应,而不依赖于细胞内的雄激素位点。在本工作中,我们探索了睾酮-BSA 在两个经过特别修饰的途径中的作用,这两个途径是通过早期转录组分析揭示的,即非基因靶向雄激素信号和 HIF1alpha 途径。我们提供的证据表明,p38 MAPK 和 PI3K/Akt/NFkappaB 和/或 Rho/Actin 途径直接参与了睾酮诱导的细胞凋亡,而 JNK/c-JUN 途径则参与了膜结合位点启动的转录。此外,我们还表明,膜作用雄激素修饰了促红细胞生成素受体 (EPOR) 的转录,导致促红细胞生成素引发的作用。有趣的是,重组人促红细胞生成素 (rHuEPO) 与睾酮-BSA 的联合使用通过离散的信号事件保护细胞免受凋亡。睾酮-BSA 的作用是通过经典的促红细胞生成素启动子发挥的,而 rHuEPO 通过其已知启动子上游的新鉴定的调节/启动子区域降低 EPOR 的转录,从而发挥作用。这些结果表明膜作用雄激素与 EPOR 之间存在新的相互作用,在乳腺癌患者的药物操作中应予以考虑。