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首页> 外文期刊>The Journal of Steroid Biochemistry and Molecular Biology >Mechanisms of drug resistance that target the androgen axis in castration resistant prostate cancer (CRPC)
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Mechanisms of drug resistance that target the androgen axis in castration resistant prostate cancer (CRPC)

机译:靶向抗抗抗腺轴抗腐蚀前列腺癌(CRPC)的耐药机制(CRPC)

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摘要

Castrate resistant prostate cancer (CRPC) is the fatal-form of prostate cancer and remains androgen dependent. The reactivation of the androgen axis occurs due to adaptive intratumoral androgen biosynthesis which can be driven by adrenal androgens and/or by changes in the androgen receptor (AR) including AR gene amplification. These mechanisms are targeted with P450c17 inhibitors e.g., abiraterone acetate and AR super-antagonists e.g., enzalutamide, respectively. Clinical experience indicates that with either agent an initial response is followed by drug resistance and the patient clinically progresses on these agents. This article reviews the mechanisms of intrinsic and acquired drug resistance that target the androgen axis and how this might be surmounted. (C) 2015 Elsevier Ltd. All rights reserved.
机译:抗抗抗原前列腺癌(CRPC)是前列腺癌的致命形式,仍然雄激素依赖。 由于适应性的肿瘤内雄激素生物合成而发生雄激素轴的再活化,其可以由肾上腺雄激素和/或通过包括AR基因扩增的雄激素受体(AR)的变化来驱动。 这些机制靶向P450C17抑制剂,例如,ABIRATERONE乙酸酯和AR超级拮抗剂,分别为依甲醛酰胺。 临床经验表明,通过任一剂,初始反应之后是耐药性,患者对这些药剂进行临床进行。 本文审查了靶向雄激素轴的内在和获得的耐药性的机制以及如何估计。 (c)2015 Elsevier Ltd.保留所有权利。

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