Department of Physiology, University of Tübingen, Germany.
Mol Cancer. 2009 Dec 1;8:114. doi: 10.1186/1476-4598-8-114.
Membrane androgen receptors (mAR) have been implicated in the regulation of cell growth, motility and apoptosis in prostate and breast cancer. Here we analyzed mAR expression and function in colon cancer.
Using fluorescent mAR ligands we showed specific membrane staining in colon cell lines and mouse xenograft tumor tissues, while membrane staining was undetectable in healthy mouse colon tissues and non-transformed intestinal cells. Saturation/displacement assays revealed time- and concentration-dependent specific binding for testosterone with a KD of 2.9 nM. Stimulation of colon mAR by testosterone albumin conjugates induced rapid cytoskeleton reorganization and apoptotic responses, even in the presence of anti-androgens. The actin cytoskeleton drug cytochalasin B effectively inhibited the pro-apoptotic responses and caspase-3 activation. Interestingly, in vivo studies revealed that mAR activation resulted in a 65% reduction of tumor incidence in chemically induced Balb/c mice colon tumors.
Our results demonstrate for the first time that functional mARs are predominantly expressed in colon tumors and that their activation results in induction of anti-tumor responses in vitro and extensive reduction of tumor incidence in vivo.
膜雄激素受体(mAR)被认为参与调节前列腺癌和乳腺癌中的细胞生长、运动和凋亡。在这里,我们分析了结肠癌中的 mAR 表达和功能。
使用荧光 mAR 配体,我们在结肠细胞系和小鼠异种移植肿瘤组织中显示出特异性的膜染色,而在健康的小鼠结肠组织和非转化的肠细胞中则无法检测到膜染色。饱和/置换分析显示,睾酮与 KD 值为 2.9 nM 的时间和浓度依赖性特异性结合。睾酮白蛋白缀合物刺激结肠 mAR 诱导快速细胞骨架重排和凋亡反应,即使存在抗雄激素。肌动蛋白细胞骨架药物细胞松弛素 B 可有效抑制促凋亡反应和 caspase-3 激活。有趣的是,体内研究表明,mAR 激活导致化学诱导的 Balb/c 小鼠结肠癌肿瘤发生率降低 65%。
我们的研究结果首次证明功能性 mAR 主要在结肠癌中表达,其激活可在体外诱导抗肿瘤反应,并在体内广泛降低肿瘤发生率。