| Literature DB >> 29894694 |
Sarah M Greenblatt1, Na Man1, Pierre-Jacques Hamard1, Takashi Asai1, Daniel Karl1, Concepcion Martinez1, Daniel Bilbao1, Vasileios Stathias2, Anna M Jermakowicz2, Stephanie Duffort1, Madhavi Tadi1, Ezra Blumenthal1, Samantha Newman1, Ly Vu3, Ye Xu4, Fan Liu4, Stephan C Schurer5, Michael T McCabe6, Ryan G Kruger6, Mingjiang Xu4, Feng-Chun Yang4, Daniel G Tenen7, Justin Watts8, Francisco Vega9, Stephen D Nimer10.
Abstract
Chromatin-modifying enzymes, and specifically the protein arginine methyltransferases (PRMTs), have emerged as important targets in cancer. Here, we investigated the role of CARM1 in normal and malignant hematopoiesis. Using conditional knockout mice, we show that loss of CARM1 has little effect on normal hematopoiesis. Strikingly, knockout of Carm1 abrogates both the initiation and maintenance of acute myeloid leukemia (AML) driven by oncogenic transcription factors. We show that CARM1 knockdown impairs cell-cycle progression, promotes myeloid differentiation, and ultimately induces apoptosis. Finally, we utilize a selective, small-molecule inhibitor of CARM1 to validate the efficacy of CARM1 inhibition in leukemia cells in vitro and in vivo. Collectively, this work suggests that targeting CARM1 may be an effective therapeutic strategy for AML.Entities:
Keywords: AML; AML1-ETO; CARM1; MLL-AF9; acute myeloid leukemia; arginine methyltransferase; epigenetics
Mesh:
Substances:
Year: 2018 PMID: 29894694 PMCID: PMC6191185 DOI: 10.1016/j.ccell.2018.05.007
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743