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Degradation of Androgen Receptor through Small Molecules for Prostate Cancer

机译:通过前列腺癌小分子降解雄激素受体

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摘要

Prostate cancer is the most common carcinoma among aged males in western countries and more aggressive and lethal castration resistant prostate cancer often occurs after androgen deprivation therapy. The high expression of androgens and androgen receptor is closely related to prostate cancer. Efficient androgen receptor antagonists, such as enzalutamide and ARN-509, could be employed as potent anti-prostate cancer agents. Nevertheless, recent studies have revealed that F876L mutation in androgen receptor converts the action of enzalutamide and ARN-509 from an antagonist to agonist, so that novel strategies are urgent to address this resistance mechanism. In this review, we focus on the discussion about some novel strategies, which targets androgen receptor mainly through the degrading pathway as potential treatments for prostate cancer.
机译:前列腺癌是西方人年龄较大的癌症中最常见的癌,并且在雄激素剥夺治疗后通常会发生更具侵略性和致命的前列腺癌。 雄激素和雄激素受体的高表达与前列腺癌密切相关。 高效的雄激素受体拮抗剂,例如烯醇酰胺和ARN-509,可以用作有效的抗前列腺癌试剂。 然而,最近的研究表明,雄激素受体中的F876L突变将苯甲甲酰胺和ARN-509的作用转化为激动剂的拮抗剂,从而迫切地解决这种阻力机制。 在这篇综述中,我们专注于有关一些新型策略的讨论,该策略主要通过降解途径作为前列腺癌的潜在治疗。

著录项

  • 来源
    《Current cancer drug targets》 |2018年第7期|共16页
  • 作者单位

    China Pharmaceut Univ Jiangsu Key Lab Drug Design &

    Optimizat 24 Tongjiaxiang Nanjing 210009;

    China Pharmaceut Univ Jiangsu Key Lab Drug Design &

    Optimizat 24 Tongjiaxiang Nanjing 210009;

    China Pharmaceut Univ Jiangsu Key Lab Drug Design &

    Optimizat 24 Tongjiaxiang Nanjing 210009;

    China Pharmaceut Univ Jiangsu Key Lab Drug Design &

    Optimizat 24 Tongjiaxiang Nanjing 210009;

    China Pharmaceut Univ Jiangsu Key Lab Drug Design &

    Optimizat 24 Tongjiaxiang Nanjing 210009;

    China Pharmaceut Univ Jiangsu Key Lab Drug Design &

    Optimizat 24 Tongjiaxiang Nanjing 210009;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

    Resistance mechanism; androgen receptor; degradation; prostate cancer; small molecules; new strategies;

    机译:抗性机制;雄激素受体;降解;前列腺癌;小分子;新策略;

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