| Literature DB >> 35525905 |
Dongxu Li1,2, Xufen Yu3,4, Jithesh Kottur3,4, Weida Gong1, Zhao Zhang5, Aaron J Storey6, Yi-Hsuan Tsai1, Hidetaka Uryu1,2, Yudao Shen3,4, Stephanie D Byrum6, Rick D Edmondson6, Samuel G Mackintosh6, Ling Cai1,7, Zhijie Liu5, Aneel K Aggarwal4, Alan J Tackett6, Jing Liu3,4, Jian Jin8,9, Gang Greg Wang10,11,12.
Abstract
WD repeat domain 5 (WDR5), an integral component of the MLL/KMT2A lysine methyltransferase complex, is critically involved in oncogenesis and represents an attractive onco-target. Inhibitors targeting protein-protein interactions (PPIs) between WDR5 and its binding partners, however, do not inhibit all of WDR5-mediated oncogenic functions and exert rather limited antitumor effects. Here, we report a cereblon (CRBN)-recruiting proteolysis targeting chimera (PROTAC) of WDR5, MS40, which selectively degrades WDR5 and the well-established neo-substrates of immunomodulatory drugs (IMiDs):CRBN, the Ikaros zinc finger (IKZF) transcription factors IKZF1 and IKZF3. MS40-induced WDR5 degradation caused disassociation of the MLL/KMT2A complex off chromatin, resulting in decreased H3K4me2. Transcriptomic profiling revealed that targets of both WDR5 and IMiDs:CRBN were significantly repressed by treatment of MS40. In MLL-rearranged leukemias, which exhibit IKZF1 high expression and dependency, co-suppression of WDR5 and Ikaros by MS40 is superior in suppressing oncogenesis to the WDR5 PPI inhibitor, to MS40's non-PROTAC analog controls (MS40N1 and MS40N2, which do not bind CRBN and WDR5, respectively), and to a matched VHL-based WDR5 PROTAC (MS169, which degrades WDR5 but not Ikaros). MS40 suppressed the growth of primary leukemia patient cells in vitro and patient-derived xenografts in vivo. Thus, dual degradation of WDR5 and Ikaros is a promising anti-cancer strategy.Entities:
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Year: 2022 PMID: 35525905 PMCID: PMC9189076 DOI: 10.1038/s41388-022-02340-8
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 8.756