Department of Molecular Cell Biology, Institute of Biochemistry, Vilnius University, LT 08662 Vilnius, Lithuania.
Department of Molecular Cell Biology, Institute of Biochemistry, Vilnius University, LT 08662 Vilnius, Lithuania.
Leuk Res. 2014 Jul;38(7):822-9. doi: 10.1016/j.leukres.2014.04.003. Epub 2014 Apr 18.
The involvement of histone lysine methyltransferases (HMT) in carcinogenesis is not well understood. Here, we describe a dose-dependent growth and survival inhibitory effects of BIX-01294, a specific inhibitor of euchromatic HMT2, in promyelocytic leukemia HL-60 and NB4 cells. BIX-01294 combined with all-trans retinoic acid or together with histone deacetylase and DNA methyltransferase inhibitors enhanced cell differentiation to granulocytes and induced cell line-specific changes in the expression of cell cycle-, survival- and differentiation regulating genes and proteins in association with histone modification state. Our results suggest that targeting EHMT2 may be of therapeutical benefits in myeloid leukemia.
组蛋白赖氨酸甲基转移酶(HMT)在癌症发生中的作用尚不清楚。在这里,我们描述了特异性的 euchromatic HMT2 抑制剂 BIX-01294 在早幼粒细胞白血病 HL-60 和 NB4 细胞中的剂量依赖性生长和存活抑制作用。BIX-01294 与全反式维甲酸联合使用,或与组蛋白去乙酰化酶和 DNA 甲基转移酶抑制剂联合使用,可增强细胞向粒细胞的分化,并诱导细胞系特异性的细胞周期、存活和分化调节基因和蛋白的表达变化,与组蛋白修饰状态相关。我们的结果表明,靶向 EHMT2 可能对髓系白血病具有治疗益处。