Selective Estrogen Receptor Degraders (SERDs): A Promising Strategy for Estrogen Receptor Positive Endocrine-Resistant Breast Cancer

被引:77
作者
Lu, Yunlong [1 ,2 ]
Liu, Wukun [1 ,3 ,4 ]
机构
[1] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Chinese Med Resour, Sch Med & Holist Integrat Med, Nanjing 210023, Peoples R China
[2] Univ Illinois, Coll Pharm, Dept Pharmaceut Sci, Chicago, IL 60612 USA
[3] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[4] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
ER-ALPHA; PURE ANTIESTROGEN; AROMATASE INHIBITORS; TAMOXIFEN RESISTANCE; UDP-GLUCURONOSYLTRANSFERASE; DOWNREGULATORS SERDS; ORAL BIOAVAILABILITY; ADJUVANT TAMOXIFEN; ENDOMETRIAL CANCER; ANTITUMOR-ACTIVITY;
D O I
10.1021/acs.jmedchem.0c00913
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Estrogen receptor (ER) plays important roles in gene transcription and the proliferation of ER positive breast cancers. Selective modulation of ER has been a therapeutic target for this specific type of breast cancer for more than 30 years. Selective estrogen receptor modulators (SERMs) and aromatase inhibitors (AIs) have been demonstrated to be effective therapeutic approaches for ER positive breast cancers. Unfortunately, 30-50% of ER positive tumors become resistant to SERM/AI treatment after 3-5 years. Fulvestrant, the only approved selective estrogen receptor degrader (SERD), is currently an important therapeutic approach for the treatment of endocrine-resistant breast cancers. The poor pharmacokinetic properties of fulvestrant have inspired the development of a new generation of oral SERDs to overcome drug resistance. In this review, we describe recent advances in ER alpha structure, functions, and mechanisms of endocrine resistance and summarize the development of oral SERDs in both academic and industrial areas.
引用
收藏
页码:15094 / 15114
页数:21
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