Combs Res. Bldg., Rm. 306, University of Kentucky Medical Center, Lexington, KY 40536, USA.
FASEB J. 2010 Mar;24(3):769-77. doi: 10.1096/fj.09-136994. Epub 2009 Nov 9.
Androgens are functionally required for the normal growth of the prostate gland and in prostate tumor development and progression. Epithelial-mesenchymal-transition (EMT) is an important process during normal development and in cancer cell metastasis induced by factors within the microenvironment, such as transforming growth factor-beta (TGF-beta). This study examined the ability of androgens to influence EMT of prostate cancer epithelial cells. The EMT pattern was evaluated on the basis of expression of the epithelial markers E-cadherin/beta-catenin, and the mesenchymal markers N-cadherin, as well as cytoskeleton reorganization in response to 5alpha-dihydrotestosterone (DHT; 1 nM) and/or TGF-beta (5 ng/ml). Overexpressing and silencing approaches to regulate androgen receptor (AR) expression were conducted to determine the involvement of AR in EMT in the presence or absence of an AR antagonist. Our results demonstrate that androgens induce the EMT pattern in prostate tumor epithelial cell with Snail activation and lead to significant changes in prostate cancer cell migration and invasion potential. Expression levels of AR inversely correlated with androgen-mediated EMT in prostate tumor epithelial cells, pointing to a low AR content required for the EMT phenotype. These findings indicate the ability of androgens to induce EMT by potentially bypassing the functional involvement of TGF-beta, thus contributing to metastatic behavior of prostate cancer cells.-Zhum, M.-L., Kyprianou, N. Role of androgens and the androgen receptor in epithelial-mesenchymal transition and invasion of prostate cancer cells.
雄激素对于前列腺的正常生长以及前列腺肿瘤的发生和发展是必需的。上皮间质转化(EMT)是正常发育过程中的一个重要过程,也是肿瘤细胞在微环境中诱导因子(如转化生长因子-β[TGF-β])作用下转移的重要过程。本研究探讨了雄激素影响前列腺癌细胞 EMT 的能力。通过上皮标志物 E-钙粘蛋白/β-连环蛋白、间质标志物 N-钙粘蛋白的表达以及细胞骨架对 5α-二氢睾酮(DHT;1 nM)和/或 TGF-β(5 ng/ml)的反应,评估 EMT 模式。采用过表达和沉默方法调节雄激素受体(AR)的表达,以确定 AR 在 AR 拮抗剂存在或不存在的情况下是否参与 EMT。我们的结果表明,雄激素诱导前列腺肿瘤上皮细胞发生 EMT,激活 Snail,并导致前列腺癌细胞迁移和侵袭潜能发生显著变化。AR 的表达水平与雄激素介导的前列腺肿瘤上皮细胞 EMT 呈负相关,这表明 EMT 表型需要低 AR 含量。这些发现表明,雄激素通过潜在地绕过 TGF-β 的功能参与,诱导 EMT,从而促进前列腺癌细胞的转移行为。-朱美莲,N. 雄激素和雄激素受体在前列腺癌细胞上皮间质转化和侵袭中的作用。