Ben May Department for Cancer Research, The University of Chicago, Chicago, Illinois.
Endocrinology. 2019 Apr 1;160(4):759-769. doi: 10.1210/en.2018-01095.
One in eight women will be diagnosed with breast cancer in their lifetime. Because estrogen receptor-α (ERα) is expressed in ~70% of patients, therapeutic intervention by ERα-targeted endocrine therapies remains the leading strategy to prevent progression and/or metastasis in the adjuvant setting. However, the efficacy of these therapies will be diminished by the development of acquired resistance after prolonged treatment regimens. In preclinical models of endocrine-resistant metastatic breast cancers that retain ERα expression, antiestrogens with improved efficacy and potency can overcome resistance to shrink tumors and prevent metastasis. In particular, selective ER degraders or downregulators, which both antagonize ERα actions and induce its degradation, have demonstrated substantial antitumor efficacy in this setting. In the present review, we have discussed the mechanisms of acquired endocrine resistance in luminal breast cancers and the strategies used by next-generation endocrine therapies to antagonize ERα.
一生中,每 8 名女性中就会有 1 名被诊断患有乳腺癌。由于雌激素受体-α(ERα)在约 70%的患者中表达,因此针对 ERα 的内分泌治疗仍然是预防辅助治疗中进展和/或转移的主要策略。然而,在长期治疗方案后,获得性耐药的发展会降低这些疗法的疗效。在保留 ERα表达的内分泌耐药转移性乳腺癌的临床前模型中,具有改善疗效和效力的抗雌激素药物可以克服耐药性,缩小肿瘤并预防转移。特别是选择性 ER 降解剂或下调剂,它们都拮抗 ERα 的作用并诱导其降解,在这种情况下已显示出显著的抗肿瘤疗效。在本综述中,我们讨论了腔面乳腺癌中获得性内分泌耐药的机制以及下一代内分泌疗法用于拮抗 ERα 的策略。