Steiner M S, Raghow S, Neubauer B L
Department of Urology, University of Tennessee, Memphis, Tennessee 38104, USA.
Urology. 2001 Apr;57(4 Suppl 1):68-72. doi: 10.1016/s0090-4295(00)00944-4.
The ability to interfere with prostate carcinogenesis, and as a consequence, prevent prostate cancer with drugs is the basis for chemoprevention. The prostate contains estrogen receptors in both the stroma and epithelium. Both animal models and human epidemiologic studies have implicated estrogens as an initiator of prostate cancer. In the aging male, prostate cancer occurs in an environment of rising estrogen and decreasing androgen levels. Selective estrogen receptor modulators (SERMs) have shown the ability to prevent (GTx-006 [acapodene]) and treat (GTx-006 and arzoxifene) prostate cancer, suggesting that they may be used in prostate cancer chemoprevention. A phase 2 clinical trial using GTx-006 for prostate cancer chemoprevention is currently being conducted.
干扰前列腺癌发生并因此用药物预防前列腺癌的能力是化学预防的基础。前列腺的基质和上皮中均含有雌激素受体。动物模型和人类流行病学研究均表明雌激素是前列腺癌的引发因素。在老年男性中,前列腺癌发生于雌激素水平上升和雄激素水平下降的环境中。选择性雌激素受体调节剂(SERM)已显示出预防(GTx-006 [阿波烯])和治疗(GTx-006和阿佐昔芬)前列腺癌的能力,这表明它们可能用于前列腺癌的化学预防。目前正在进行一项使用GTx-006进行前列腺癌化学预防的2期临床试验。