Selective Estrogen receptor degraders (SERDs) for the treatment of breast cancer: An overview

dc.contributor.authorBhatia, Neha
dc.contributor.authorHazra, Shreejita
dc.contributor.authorThareja, Suresh
dc.date.accessioned2024-01-21T10:38:33Z
dc.date.accessioned2024-08-13T12:05:30Z
dc.date.available2024-01-21T10:38:33Z
dc.date.available2024-08-13T12:05:30Z
dc.date.issued2023-05-04T00:00:00
dc.description.abstractDiscovery of SERDs has changed the direction of anticancer research, as more than 70% of breast cancer cases are estrogen receptor positive (ER+). Therapies such as selective estrogen receptor modulators (SERM) and aromatase inhibitors (AI's) have been effective, but due to endocrine resistance, SERDs are now considered essential therapeutics for the treatment of ER+ breast cancer. The present review deliberates the pathophysiology of SERDs from the literature covering various molecules in clinical trials. Estrogen receptors active sites distinguishing characteristics and interactions with currently available FDA-approved drugs have also been discussed. Designing strategy of previously reported SERDs, their SAR analysis, in silico, and the biological efficacy have also been summarized along with appropriate examples. � 2023 Elsevier Masson SASen_US
dc.identifier.doi10.1016/j.ejmech.2023.115422
dc.identifier.issn2235234
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3602
dc.identifier.urlhttps://linkinghub.elsevier.com/retrieve/pii/S0223523423003884
dc.language.isoen_USen_US
dc.publisherElsevier Masson s.r.l.en_US
dc.subjectAnti-estrogenicen_US
dc.subjectAromataseen_US
dc.subjectBreast canceren_US
dc.subjectElacestranten_US
dc.subjectER-?en_US
dc.subjectER-?en_US
dc.subjectEstrogenen_US
dc.subjectFulvestranten_US
dc.subjectOrserduen_US
dc.subjectSelective estrogen receptor degraders (SERDs)en_US
dc.subjectSERMen_US
dc.titleSelective Estrogen receptor degraders (SERDs) for the treatment of breast cancer: An overviewen_US
dc.title.journalEuropean Journal of Medicinal Chemistryen_US
dc.typeReviewen_US
dc.type.accesstypeClosed Accessen_US

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