| Literature DB >> 30640450 |
Victoria A Assimon1, Yangzhong Tang1, Jesse D Vargas1, Grace J Lee1, Zhi Yong Wu1, Kenny Lou1, Bing Yao1, Mary-Kamala Menon1, Ariel Pios1, Kristy C Perez1, Antonett Madriaga1, Peter K Buchowiecki1, Mark Rolfe1, Laura Shawver1, Xianyun Jiao1, Ronan Le Moigne1, Han-Jie Zhou1, Daniel J Anderson1.
Abstract
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.Entities:
Year: 2019 PMID: 30640450 DOI: 10.1021/acschembio.8b00904
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100