Oral Selective Estrogen Receptor Downregulators (SERDs), a Breakthrough Endocrine Therapy for Breast Cancer.

Abstract

Drugs that inhibit estrogen receptor alpha (ERα) or that block the production of estrogens remain frontline interventions in the treatment and management of breast cancer at all stages. However, resistance to endocrine therapies, especially in the setting of advanced disease, remains an impediment to durable clinical responses. Although the mechanisms underlying resistance to existing agents are complex, preclinical studies suggest that selective estrogen receptor downregulators (SERDs), molecules which eliminate ERα expression, may have particular utility in the treatment of breast cancers that have progressed on tamoxifen and/or aromatase inhibitors. The discovery and development of orally bioavailable SERDs provide the opportunity to evaluate the utility of eliminating ERα expression in advanced metastatic breast cancers.

• Authors: Donald P McDonnell, Suzanne E Wardell, John D Norris
• Journal: Journal of medicinal chemistry (J Med Chem) Vol. 58 Issue 12 Pg. 4883-7 (Jun 25 2015) ISSN: 1520-4804 [Electronic] United States
• PMID: 26039356 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Antineoplastic Agents, Hormonal
• Aromatase Inhibitors
• Estrogen Receptor alpha
• Selective Estrogen Receptor Modulators
• Tamoxifen

Topics

• Animals
• Antineoplastic Agents, Hormonal (chemistry, pharmacology)
• Aromatase Inhibitors (chemistry, pharmacology)
• Breast (drug effects, metabolism)
• Breast Neoplasms (drug therapy, metabolism)
• Drug Discovery
• Estrogen Receptor alpha (metabolism)
• Female
• Humans
• Selective Estrogen Receptor Modulators (chemistry, pharmacology)
• Tamoxifen (analogs & derivatives, pharmacology)