Recent progress in selective estrogen receptor downregulators (SERDs) for the treatment of breast cancer

被引:39
作者
Shagufta [1 ]
Ahmad, Irshad [1 ]
Mathew, Shimy [2 ]
Rahman, Sofia [2 ]
机构
[1] Amer Univ Ras Al Khaimah, Dept Math & Nat Sci, Sch Arts & Sci, POB 10021, Ras Al Khaymah, U Arab Emirates
[2] Amer Univ Ras Al Khaimah, Dept Biotechnol, Sch Arts & Sci, POB 10021, Ras Al Khaymah, U Arab Emirates
来源
RSC MEDICINAL CHEMISTRY | 2020年 / 11卷 / 04期
关键词
TARGETING CHIMERAS PROTACS; FULVESTRANT; 500; MG; ER-ALPHA; AROMATASE INHIBITORS; POSTMENOPAUSAL WOMEN; ENDOCRINE THERAPY; DOUBLE-BLIND; BIOLOGICAL EVALUATION; PHASE-II; UDP-GLUCURONOSYLTRANSFERASE;
D O I
10.1039/c9md00570f
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Selective estrogen receptor downregulators (SERDs) are a novel class of compounds capable of reducing the ER alpha protein level and blocking ER activity. Therefore, SERDs are considered as a significant therapeutic approach to treat ER+ breast cancer in both early stage and more advanced drug-resistant cases. After the FDA approval of a steroidal drug, fulvestrant, as a SERD for the treatment of breast cancer in patients who have progressed on antihormonal agents, several molecules with diverse chemical structures have been rapidly developed, studied and evaluated for selective estrogen receptor downregulation activity. Here we compile the promising SERDs reported in recent years and discuss the chemical structure and pharmacological profile of the most potent compound of the considered series. Because of the availability of only a limited number of effective drugs for the treatment of breast cancer, the quest for a potent SERD with respectable activity and bioavailability is still ongoing. The goal of this article is to make available to the reader an overview of the current progress in SERDs and provide clues for the future discovery and development of novel pharmacological potent SERDs for the treatment of breast cancer.
引用
收藏
页码:438 / 454
页数:17
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