Identification of a CARM1 Inhibitor with Potent In Vitro and In Vivo Activity in Preclinical Models of Multiple Myeloma. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Drew, Allison; Moradei, Oscar; Jacques, Suzanne; Rioux, Nathalie; Boriack-Sjodin, Ann; Allain, Christina; Scott, Margaret; Jin, Lei; Raimondi, Alejandra; Handler, Jessica; Ott, Heidi; Kruger, Ryan; McCabe, Michael; Sneeringer, Christopher; Riera, Thomas; Shapiro, Gideon; Waters, Nigel; Mitchell, Lorna; Duncan, Kenneth; Moyer, Mikel; Copeland, Robert; Smith, Jesse; Chesworth, Richard; Ribich, Scott
• Is Part Of: Scientific reports. Volume 7:Issue 1(2017)
• Page Start: 1
• Page End: 13
• Publication Date: 2017-12
• Subjects: Natural history -- Research -- Periodicals; Biology -- Research -- Periodicals; Physical sciences -- Research -- Periodicals; Earth sciences -- Research -- Periodicals; Environmental sciences -- Research -- Periodicals; 502.85
• DOI: 10.1038/s41598-017-18446-z
• Languages: English
• ISSNs: 2045-2322

Abstract

Abstract CARM1 is an arginine methyltransferase with diverse histone and non-histone substrates implicated in the regulation of cellular processes including transcriptional co-activation and RNA processing. CARM1 overexpression has been reported in multiple cancer types and has been shown to modulate oncogenic pathways inin vitro studies. Detailed understanding of the mechanism of action of CARM1 in oncogenesis has been limited by a lack of selective tool compounds, particularly forin vivo studies. We describe the identification and characterization of, to our knowledge, the first potent and selective inhibitor of CARM1 that exhibits anti-proliferative effects bothin vitro andin vivo and, to our knowledge, the first demonstration of a role for CARM1 in multiple myeloma (MM). EZM2302 (GSK3359088) is an inhibitor of CARM1 enzymatic activity in biochemical assays (IC50 = 6 nM) with broad selectivity against other histone methyltransferases. Treatment of MM cell lines with EZM2302 leads to inhibition of PABP1 and SMB methylation and cell stasis with IC50 values in the nanomolar range. Oral dosing of EZM2302 demonstrates dose-dependentin vivo CARM1 inhibition and anti-tumor activity in an MM xenograft model. EZM2302 is a validated chemical probe suitable for further understanding the biological role CARM1 plays in cancer and other diseases.