Ichikawa Tomohiko, Suzuki Hiroyoshi, Ueda Takeshi, Komiya Akira, Imamoto Takashi, Kojima Satoko
Department of Urology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Cancer Chemother Pharmacol. 2005 Nov;56 Suppl 1:58-63. doi: 10.1007/s00280-005-0100-x.
Most prostate cancers are androgen-dependent and essentially respond to androgen ablation therapy. However, these tumors eventually become androgen-independent and progress despite androgen ablation. Since the androgen receptor (AR) sequence was determined, numerous studies have shown that AR plays a critical role in the development of androgen-refractory prostate cancer. Amplification of AR, mutations of AR, and deregulation of growth factors, cytokines and AR co-activators, which could be classified as AR-dependent pathways, are frequently observed in this condition. There are other pathways, AR-independent pathways that bypass AR, which involve neuroendocrine differentiation of prostate cancer cells, deregulation of apoptotic genes and unknown mechanisms related to down-regulation of AR. Androgen-refractory prostate cancers with the AR-dependent pathway could be treated by suppressing AR activity, whereas AR-independent tumors would require alternative management strategies. When more cell survival pathways are defined, improvement of patients' survival could be achieved by developing specific gene-targeting therapies that interfere with those pathways.
大多数前列腺癌是雄激素依赖性的,本质上对雄激素剥夺疗法有反应。然而,这些肿瘤最终会变得雄激素非依赖性,尽管进行了雄激素剥夺仍会进展。自从雄激素受体(AR)序列被确定以来,大量研究表明AR在雄激素难治性前列腺癌的发展中起关键作用。在这种情况下,经常观察到AR的扩增、AR的突变以及生长因子、细胞因子和AR共激活因子的失调,这些可归类为AR依赖性途径。还有其他途径,即绕过AR的AR非依赖性途径,这涉及前列腺癌细胞的神经内分泌分化、凋亡基因的失调以及与AR下调相关的未知机制。具有AR依赖性途径的雄激素难治性前列腺癌可以通过抑制AR活性来治疗,而AR非依赖性肿瘤则需要替代的管理策略。当更多的细胞存活途径被确定时,通过开发干扰这些途径的特定基因靶向疗法可以提高患者的生存率。