Louis Warschaw Prostate Cancer Center, Sumner M. Redstone Prostate Cancer Research Program, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Prostate. 2010 Aug;70(11):1201-10. doi: 10.1002/pros.21155.
Previously, we identified Beta-2-microglobulin (beta2M) as an androgen-regulated secreted protein elevated in the serum of prostate cancer patients. In this study, we explore an interaction between beta2M expression, prostate cancer tissue, and the androgen signaling axis.
beta2M expression in relation to clinical and pathologic variables was examined in a tissue microarray representing specimens obtained at the time of radical prostatectomy. Viral vectors were designed to down-regulate beta2M expression, and the effects on androgen-dependent growth, transcriptional regulation, and androgen receptor recruitment was investigated in human prostate cancer cell lines.
Variation in beta2M expression in human prostate cancer is associated with characteristics of clinically aggressive disease such as high tumor grade. Knockdown of beta2M expression in human prostate cancer cells resulted in selective defects in androgen-dependent events including growth, gene regulation, and chromatin assembly.
beta2M expression may provide prognostic information in patients treated with surgery for prostate cancer. Targeting beta2M expression or activity may represent a new and important mechanism to manipulate the androgen signaling axis in patients with prostate cancer.
此前,我们发现β2-微球蛋白(β2M)是雄激素调控的分泌蛋白,在前列腺癌患者的血清中升高。在这项研究中,我们探讨了β2M 表达、前列腺癌组织与雄激素信号轴之间的相互作用。
在代表根治性前列腺切除术时获得的标本的组织微阵列中,检查了β2M 表达与临床和病理变量的关系。设计了病毒载体以下调β2M 的表达,并在人前列腺癌细胞系中研究了其对雄激素依赖性生长、转录调控和雄激素受体募集的影响。
人前列腺癌中β2M 表达的变化与具有侵袭性临床特征的疾病有关,例如高肿瘤分级。在人前列腺癌细胞中敲低β2M 的表达导致雄激素依赖性事件(包括生长、基因调控和染色质组装)的选择性缺陷。
β2M 表达可能为接受手术治疗的前列腺癌患者提供预后信息。靶向β2M 的表达或活性可能代表一种新的重要机制,可用于操纵前列腺癌患者的雄激素信号轴。