Rhodium(II) Proximity-Labeling Identifies a Novel Target Site on STAT3 for Inhibitors with Potent Anti-Leukemia Activity.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION(2015)

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摘要
Nearly 40% of children with acute myeloid leukemia (AML) suffer relapse arising from chemoresistance, often involving upregulation of the oncoprotein STAT3 (signal transducer and activator of transcription3). Herein, rhodium(II)-catalyzed, proximity-driven modification identifies the STAT3 coiled-coil domain (CCD) as a novel ligand-binding site, and we describe a new naphthalene sulfonamide inhibitor that targets the CCD, blocks STAT3 function, and halts its disease-promoting effects invitro, in tumor growth models, and in a leukemia mouse model, validating this new therapeutic target for resistant AML.
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关键词
anti-tumor agents,leukemia,protein modifications,rhodium,stat3
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