| Literature DB >> 26480340 |
Matthew B Minus1, Wei Liu2, Farrukh Vohidov1, Moses M Kasembeli3, Xin Long2, Michael J Krueger2, Alexandra Stevens2, Mikhail I Kolosov2, David J Tweardy4, Edward Allan R Sison2, Michele S Redell5, Zachary T Ball6.
Abstract
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 transcription 3). 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 in vitro, in tumor growth models, and in a leukemia mouse model, validating this new therapeutic target for resistant AML.Entities:
Keywords: anti-tumor agents; leukemia; protein modifications; rhodium; stat3
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Year: 2015 PMID: 26480340 PMCID: PMC5041597 DOI: 10.1002/anie.201506889
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336