Culig Z, Stober J, Gast A, Peterziel H, Hobisch A, Radmayr C, Hittmair A, Bartsch G, Cato A C, Klocker H
Department of Urology, University of Innsbruck, Austria.
Cancer Detect Prev. 1996;20(1):68-75.
The androgen receptor (AR) plays a central regulatory role in prostatic carcinoma and is a target of androgen ablation therapy. Recent detection of mutant receptors in tumor specimens suggest a contribution of AR alterations to progression towards androgen independence. In a specimen derived from metastatic prostate cancer we have reported a point mutation in the AR gene that leads to a single amino acid exchange in the ligand binding domain of the receptor. Another amino acid exchange resulting from a point mutation was also identified 15 amino acids away from our mutation. This mutation was detected in the AR gene isolated from an organ-confined prostatic tumor. Here we report the functional characterization of the two mutant receptors in the presence of adrenal androgens and testosterone metabolites. These studies were performed by cotransfecting androgen-responsive reporter genes and either the wild-type or mutant AR expression vectors into receptor negative DU-145 and CV-1 cells. The indicator genes used consisted of the promoter of the androgen-inducible prostate-specific antigen gene or the C' Delta9 enhancer fragment from the promoter of the mouse sex-limited protein driving the expression of the bacterial chloramphenicol acetyl transferase gene. Cotransfection-transactivation assays revealed that the adrenal androgen androstenedione and two products of testosterone metabolism, androsterone and androstandiol, induced reporter gene activity more efficiently in the presence of the mutant receptors than in the presence of the wild-type receptor. No difference between wild-type and mutant receptors was observed in the presence of the metabolite androstandione. The interaction of receptor-hormone complexes with target DNA was studied in vitro by electrophoretic mobility shift assays (EMSA). Dihydrotestosterone and the synthetic androgen mibolerone induced a faster migrating complex with all receptors, whereas the androgen metabolite androstandione induced this complex only with the two mutant receptors. Androsterone and androstandiol were inactive in the EMSA. These aberrant properties of the mutant receptors in the presence of adrenal androgens and products of androgen metabolism may be of importance in the course of the prostate cancer, especially during androgen ablation therapy.
雄激素受体(AR)在前列腺癌中发挥着核心调节作用,并且是雄激素剥夺疗法的靶点。最近在肿瘤标本中检测到突变受体,提示AR改变对雄激素非依赖性进展有作用。在一份来自转移性前列腺癌的标本中,我们报道了AR基因中的一个点突变,该突变导致受体配体结合域中的单个氨基酸交换。在距我们的突变15个氨基酸处还鉴定出另一个由点突变导致的氨基酸交换。此突变在从器官局限性前列腺肿瘤分离的AR基因中被检测到。在此,我们报道了在存在肾上腺雄激素和睾酮代谢产物的情况下两种突变受体的功能特性。这些研究通过将雄激素反应性报告基因与野生型或突变型AR表达载体共转染到受体阴性的DU-145和CV-1细胞中来进行。所使用的指示基因包括雄激素诱导的前列腺特异性抗原基因的启动子或来自小鼠性别限制蛋白启动子的C' Delta9增强子片段,其驱动细菌氯霉素乙酰转移酶基因的表达。共转染-反式激活测定显示,在存在突变受体的情况下,肾上腺雄激素雄烯二酮以及睾酮代谢的两种产物,雄酮和雄二醇,比在存在野生型受体的情况下更有效地诱导报告基因活性。在存在代谢产物雄烷二酮的情况下,未观察到野生型和突变型受体之间的差异。通过电泳迁移率变动分析(EMSA)在体外研究了受体-激素复合物与靶DNA的相互作用。双氢睾酮和合成雄激素米勃龙与所有受体诱导出迁移更快的复合物,而雄激素代谢产物雄烷二酮仅与两种突变受体诱导出这种复合物。雄酮和雄二醇在EMSA中无活性。在存在肾上腺雄激素和雄激素代谢产物的情况下,突变受体的这些异常特性可能在前列腺癌进程中具有重要意义,尤其是在雄激素剥夺治疗期间。