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
酶
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
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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