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Mechanisms of Drug Resistance that Target the Androgen Axis in Castration Resistant Prostate Cancer (CRPC)

机译:靶向去势抵抗性前列腺癌(CRPC)中雄激素轴的耐药机制

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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. 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.
机译:去势抵抗性前列腺癌(CRPC)是前列腺癌的致命形式,仍然依赖雄激素。雄激素轴的重新激活归因于肿瘤内的适应性瘤内雄激素生物合成,这可由肾上腺雄激素和/或雄激素受体(AR)的变化(包括AR基因扩增)驱动。这些机制以P450c17抑制剂(例如乙酸阿比特龙酯和AR超级拮抗剂,例如恩杂鲁胺。临床经验表明,使用任何一种药物都会产生最初的反应,随后是耐药性,并且患者在使用这些药物后的临床进展。本文回顾了针对雄激素轴的内在和获得性耐药机制,以及如何克服这种机制。

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