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Discovery of Orally Active Inhibitors of Brahma Homolog (BRM)/SMARCA2 ATPase Activity for the Treatment of Brahma Related Gene 1 (BRG1)/SMARCA4-Mutant Cancers.
Papillon, Julien P N; Nakajima, Katsumasa; Adair, Christopher D; Hempel, Jonathan; Jouk, Andriana O; Karki, Rajeshri G; Mathieu, Simon; Möbitz, Henrik; Ntaganda, Rukundo; Smith, Troy; Visser, Michael; Hill, Susan E; Hurtado, Felipe Kellermann; Chenail, Gregg; Bhang, Hyo-Eun C; Bric, Anka; Xiang, Kay; Bushold, Geoffrey; Gilbert, Tamara; Vattay, Anthony; Dooley, Julie; Costa, Emily A; Park, Isabel; Li, Ailing; Farley, David; Lounkine, Eugen; Yue, Q Kimberley; Xie, Xiaoling; Zhu, Xiaoping; Kulathila, Raviraj; King, Daniel; Hu, Tiancen; Vulic, Katarina; Cantwell, John; Luu, Catherine; Jagani, Zainab.
Affiliation
  • Möbitz H; Global Discovery Chemistry , Novartis Institutes for Biomedical Research , Basel 4002 , Switzerland.
  • Cantwell J; Novartis Institutes for Biomedical Research , 5300 Chiron Way , Emeryville , California 94608 , United States.
  • Luu C; Novartis Institutes for Biomedical Research , 5300 Chiron Way , Emeryville , California 94608 , United States.
J Med Chem ; 61(22): 10155-10172, 2018 11 21.
Article in En | MEDLINE | ID: mdl-30339381
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Nuclear Proteins / Drug Design / DNA Helicases / Mutation / Antineoplastic Agents Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 2018 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Nuclear Proteins / Drug Design / DNA Helicases / Mutation / Antineoplastic Agents Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 2018 Document type: Article Country of publication: