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Therapeutic Strategies to Target the Androgen Receptor

dc.contributor.authorXiang, W
dc.contributor.authorWang, S
dc.coverage.spatialUnited States
dc.date.accessioned2024-01-23T21:14:18Z
dc.date.available2024-01-23T21:14:18Z
dc.date.issued2022-07-14
dc.identifier.issn0022-2623
dc.identifier.issn1520-4804
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/35786895
dc.identifier.urihttps://hdl.handle.net/2027.42/192127en
dc.description.abstractThe androgen receptor (AR) plays a key role in the maintenance of muscle and bone and the support of male sexual-related functions, as well as in the progression of prostate cancer. Accordingly, AR-targeted therapies have been developed for the treatment of related human diseases and conditions. AR agonists are an important class of drugs in the treatment of bone loss and muscle atrophy. AR antagonists have also been developed for the treatment of prostate cancer, including metastatic castration-resistant prostate cancer (mCRPC). Additionally, selective AR degraders (SARDs) have been reported. More recently, heterobifunctional degrader molecules of AR have been developed, and four such compounds are now in clinical development for the treatment of human prostate cancer. This review attempts to summarize the different types of compounds designed to target AR and the current frontiers of research on this important therapeutic target.
dc.format.mediumPrint-Electronic
dc.languageeng
dc.publisherAmerican Chemical Society (ACS)
dc.subjectAndrogen Antagonists
dc.subjectAndrogen Receptor Antagonists
dc.subjectHumans
dc.subjectMale
dc.subjectProstatic Neoplasms, Castration-Resistant
dc.subjectReceptors, Androgen
dc.titleTherapeutic Strategies to Target the Androgen Receptor
dc.typeArticle
dc.identifier.pmid35786895
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/192127/2/xiang-wang-2022-therapeutic-strategies-to-target-the-androgen-receptor.pdf
dc.identifier.doi10.1021/acs.jmedchem.2c00716
dc.identifier.doihttps://dx.doi.org/10.7302/22127
dc.identifier.sourceJournal of Medicinal Chemistry
dc.description.versionPublished version
dc.date.updated2024-01-23T21:14:16Z
dc.identifier.orcid0000-0002-8782-6950
dc.identifier.volume65
dc.identifier.issue13
dc.identifier.startpage8772
dc.identifier.endpage8797
dc.identifier.name-orcidXiang, W
dc.identifier.name-orcidWang, S; 0000-0002-8782-6950
dc.working.doi10.7302/22127en
dc.owningcollnameInternal Medicine, Department of


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