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• W4245405909 abstract "Abstract Androgen receptor (AR)‐dependent transcription is a major driver of prostate tumor cell proliferation. Consequently, it is the target of several antitumor chemotherapeutic agents, including the AR antagonist MDV3100/enzalutamide. Recent studies have shown that a single AR mutation (F876L) converts MDV3100 action from an antagonist to an agonist. Here we describe the generation of a novel class of selective androgen receptor degraders (SARDs) to address this resistance mechanism. Molecules containing hydrophobic degrons linked to small‐molecule AR ligands induce AR degradation, reduce expression of AR target genes and inhibit proliferation in androgen‐dependent prostate cancer cell lines. These results suggest that selective AR degradation may be an effective therapeutic prostate tumor strategy in the context of AR mutations that confer resistance to second‐generation AR antagonists." @default.
• W4245405909 created "2022-05-12" @default.
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• W4245405909 date "2015-06-17" @default.
• W4245405909 modified "2023-10-18" @default.
• W4245405909 title "Small-Molecule-Mediated Degradation of the Androgen Receptor through Hydrophobic Tagging" @default.
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• W4245405909 doi "https://doi.org/10.1002/ange.201503720" @default.
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