CB-6644 Is a Selective Inhibitor of the RUVBL1/2 Complex with Anticancer Activity

生物 髓系白血病 癌变 癌症研究 变构调节 染色质重塑 癌细胞 癌症 细胞生物学 染色质 生物化学 基因 遗传学
作者
Victoria A. Assimon,Yangzhong Tang,Jesse D. Vargas,Grace J. Lee,Zhi Wu,Kenny Lou,Bing Yao,Mary-Kamala Menon,Ariel Pios,Kristy C. Perez,Antonett Madriaga,Peter K. Buchowiecki,Mark Rolfe,Laura K. Shawver,Xian‐Yun Jiao,Ronan Le Moigne,Han-Jie Zhou,Daniel J. Anderson
出处
期刊:ACS Chemical Biology [American Chemical Society]
卷期号:14 (2): 236-244 被引量:93
标识
DOI:10.1021/acschembio.8b00904
摘要

RUVBL1 and RUVBL2 are ATPases associated with diverse cellular activities (AAAs) that form a complex involved in a variety of cellular processes, including chromatin remodeling and regulation of gene expression. RUVBLs have a strong link to oncogenesis, where overexpression is correlated with tumor growth and poor prognosis in several cancer types. CB-6644, an allosteric small-molecule inhibitor of the ATPase activity of the RUVBL1/2 complex, interacts specifically with RUVBL1/2 in cancer cells, leading to cell death. Importantly, drug-acquired-resistant cell clones have amino acid mutations in either RUVBL1 or RUVBL2, suggesting that cell killing is an on-target consequence of RUVBL1/2 engagement. In xenograft models of acute myeloid leukemia and multiple myeloma, CB-6644 significantly reduced tumor growth without obvious toxicity. This work demonstrates the therapeutic potential of targeting RUVBLs in the treatment of cancer and establishes a chemical entity for probing the many facets of RUVBL biology.
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