Chang K-H, Ercole C E, Sharifi N
Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
Department of Urology, Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, OH, USA.
Br J Cancer. 2014 Sep 23;111(7):1249-54. doi: 10.1038/bjc.2014.268. Epub 2014 May 27.
Despite our most vigorous efforts, prostate cancer remains the second leading cause of cancer death in men. Understanding the intricacies of androgen metabolism is vital to finding therapeutic targets, particularly with progression of advanced prostate cancer after initial hormone therapy, where adrenal precursors are involved. Such is the case with castration-resistant prostate cancer, where adrenal androgens, for example, dehydroepiandrosterone, are a source for intratumoural synthesis of dihydrotestosterone. As prostate cancer progresses, androgen metabolism changes due to altered expression of steroidogenic enzymes and mutations in the components of the steroidogenic machinery. These alterations sustain disease and allow progression; mechanistically, they may also enable development of hormone therapy resistance. With the development of the newer agents, abiraterone acetate and enzalutamide, efforts have been made to better define the basis for response and resistance. This work can be carried out in cell lines, animal models, as well as with ex vivo analysis of tissues obtained from patients. Efforts to further elucidate the finer details of the steroidogenic pathway are necessary to move toward a curative paradigm for patients with localised disease at high risk for recurrence.
尽管我们付出了最大的努力,但前列腺癌仍是男性癌症死亡的第二大主要原因。了解雄激素代谢的复杂性对于找到治疗靶点至关重要,尤其是在初始激素治疗后晚期前列腺癌进展且涉及肾上腺前体的情况下。去势抵抗性前列腺癌就是如此,例如肾上腺雄激素脱氢表雄酮是肿瘤内二氢睾酮合成的来源。随着前列腺癌的进展,由于类固醇生成酶表达的改变和类固醇生成机制成分的突变,雄激素代谢发生变化。这些改变维持疾病并使其进展;从机制上讲,它们还可能导致激素治疗耐药性的产生。随着新型药物醋酸阿比特龙和恩杂鲁胺的开发,人们努力更好地确定反应和耐药的基础。这项工作可以在细胞系、动物模型以及对患者获得的组织进行体外分析中开展。进一步阐明类固醇生成途径的更细微细节的努力对于朝着为有高复发风险的局限性疾病患者实现治愈模式迈进是必要的。