| Literature DB >> 30339381 |
Julien P N Papillon, Katsumasa Nakajima, Christopher D Adair, Jonathan Hempel, Andriana O Jouk, Rajeshri G Karki, Simon Mathieu, Henrik Möbitz1, Rukundo Ntaganda, Troy Smith, Michael Visser, Susan E Hill, Felipe Kellermann Hurtado, Gregg Chenail, Hyo-Eun C Bhang, Anka Bric, Kay Xiang, Geoffrey Bushold, Tamara Gilbert, Anthony Vattay, Julie Dooley, Emily A Costa, Isabel Park, Ailing Li, David Farley, Eugen Lounkine, Q Kimberley Yue, Xiaoling Xie, Xiaoping Zhu, Raviraj Kulathila, Daniel King, Tiancen Hu, Katarina Vulic, John Cantwell2, Catherine Luu2, Zainab Jagani.
Abstract
SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin subfamily A member 2 (SMARCA2), also known as Brahma homologue (BRM), is a Snf2-family DNA-dependent ATPase. BRM and its close homologue Brahma-related gene 1 (BRG1), also known as SMARCA4, are mutually exclusive ATPases of the large ATP-dependent SWI/SNF chromatin-remodeling complexes involved in transcriptional regulation of gene expression. No small molecules have been reported that modulate SWI/SNF chromatin-remodeling activity via inhibition of its ATPase activity, an important goal given the well-established dependence of BRG1-deficient cancers on BRM. Here, we describe allosteric dual BRM and BRG1 inhibitors that downregulate BRM-dependent gene expression and show antiproliferative activity in a BRG1-mutant-lung-tumor xenograft model upon oral administration. These compounds represent useful tools for understanding the functions of BRM in BRG1-loss-of-function settings and should enable probing the role of SWI/SNF functions more broadly in different cancer contexts and those of other diseases.Entities:
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Year: 2018 PMID: 30339381 DOI: 10.1021/acs.jmedchem.8b01318
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446