Journal of Medicinal Chemistry · 2021 · 71 citations · 29 references
MedicineMedicinal ChemistryOncologyCell SignalingDrug DesignDrug DiscoveryEnzyme FunctionHormonal Cancer TherapyLigand BindingNuclear ReceptorsSignal Transduction In CancerAromatase InhibitorsClick ChemistryClick-chemistry LinkersDna-encoded LibrariesDna-encoded Library DesignDna-encoded Library TechnologyEstrogen Receptor SignalingEstrogen Receptors
Bispecific degraders (PROTACs) of ERα are expected to be advantageous over current inhibitors of ERα signaling (aromatase inhibitors/SERMs/SERDs) used to treat ER+ breast cancer. Information from DNA-encoded chemical library (DECL) screening provides a method to identify novel PROTAC binding features as the linker positioning, and binding elements are determined directly from the screen. After screening ∼120 billion DNA-encoded molecules with ERα WT and 3 gain-of-function (GOF) mutants, with and without estradiol to identify features that enrich ERα competitively, the off-DNA synthesized small molecule exemplar 7 exhibited nanomolar ERα binding, antagonism, and degradation. Click chemistry synthesis on an alkyne E3 ligase engagers panel and an azide variant of 7 rapidly generated bispecific nanomolar degraders of ERα, with PROTACs 18 and 21 inhibiting ER+ MCF7 tumor growth in a mouse xenograft model of breast cancer. This study validates this approach toward identifying novel bispecific degrader leads from DECL screening with minimal optimization.
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Kathleen M. Sakamoto, Kyung B. Kim, Akiko Kumagai et al. · Proceedings of the National Academy of Sciences · 2001 · 2.5K citations · Full text
Catalytic in vivo protein knockdown by small-molecule PROTACs
Daniel P. Bondeson, Alina Mares, Ian E. Smith et al. · Nature Chemical Biology · 2015 · 1.3K citations · Full text
Activating ESR1 mutations in hormone-resistant metastatic breast cancer
Dan R. Robinson, Yi-Mi Wu, Pankaj Vats et al. · Nature Genetics · 2013 · 1.2K citations · Full text