Second-Generation Estrogen Receptor Down-Regulators for Medical Therapy

UCLA researchers in the School of Medicine have developed a series of novel estrogen receptor antagonists for breast cancer therapy.

Breast cancer is the most common malignancy in women in North America. Each year, more than 210,000 new cases of breast cancer are diagnosed in the US. About 70% of breast cancers depend on estrogen for growth and progression. In the clinic, endocrine therapy has proven to be one of the most effective treatment strategies for breast cancer. However, a large number of patients with localized disease and all of the patients with metastatic breast cancer become resistant to current endocrine therapies such as tamoxifen and aromatase inhibitors. Moreover, recent data suggests that roughly 14% of metastatic breast cancer harbor estrogen receptor mutations that reduce sensitivity to the widely used tamoxifen and fulvestrant, so higher doses of these antiestrogens appear to be needed to achieve good antitumor effects. Therefore, there is an urgent need to develop alternative therapeutics to overcome endocrine resistance and to improve the long-term survival of patients afflicted with breast cancer.

Researchers in UCLA School of Medicine have developed a series of novel estrogen receptor antagonists that are very effective in inhibiting the growth of breast cancer. These unique, selective estrogen receptor down-regulators optimally target the estrogen receptor for degradation and elimination, thereby blocking downstream growth-promoting signaling pathways induced by estrogen receptors in breast cancer. These never before reported compounds are more potent than fulvestrant and are effective in endocrine-resistant disease models. They exhibit the proper biologic and pharmacologic profile to be developed as therapeutics for endocrine-sensitive and -resistant cancers in the clinic.

These selective estrogen receptor down-regulators (SERDs) can be used as therapeutics for endocrine-sensitive and -resistant breast cancers.

Researchers have designed, synthesized, and tested several selective estrogen receptor down-regulators (SERDs) using in vitro human breast cancer models.