Departamento de Química Orgánica, Facultade de Química, Universidade de Vigo, 36310 Vigo, Spain.
ChemMedChem. 2012 Dec;7(12):2101-12. doi: 10.1002/cmdc.201200366. Epub 2012 Oct 9.
A novel epigenetic modulator that displays a DNMT1 inhibition and DNMT3A activation profile was characterized (compound 8). This compound is a derivative of palmitic acid that incorporates the putative reactive functional group (diynone) of the peyssonenyne natural products. Other analogues containing the diynone or an acetoxyenediyne did not show the same biological profile. In U937 human leukemia cells, diynone 8 induced cell differentiation and apoptosis, which correlated with the expression of Fas protein. Very surprisingly, diynone 8 was toxic to normal human fibroblasts (BJ) and mouse embryo fibroblasts (MEF), but not to immortalized human fibroblasts (BJEL); this unique effect was not observed with the classical DNMT inhibitor 5-azacytidine. Therefore, compound 8 interferes in a very specific manner with signaling pathways, the activities of which differ between normal and immortalized cell types. This toxicity is reminiscent of the effects of Dnmt1 ablation on mouse fibroblasts. In fact, some of the genes deregulated by the loss of Dnmt1 are similarly deregulated by 8, but not by the DNMT inhibitor SGI-1027.
一种新型的表观遗传调节剂,表现出 DNMT1 抑制和 DNMT3A 激活的特征(化合物 8)。该化合物是棕榈酸的衍生物,包含了假定的反应性功能基团(二炔酮)的 peyssonenyne 天然产物。其他含有二炔酮或乙酰氧基烯二炔的类似物没有表现出相同的生物学特征。在 U937 人白血病细胞中,二炔酮 8 诱导细胞分化和凋亡,这与 Fas 蛋白的表达相关。非常令人惊讶的是,二炔酮 8 对正常人成纤维细胞(BJ)和小鼠胚胎成纤维细胞(MEF)有毒性,但对永生化人成纤维细胞(BJEL)没有毒性;这种独特的效应在经典的 DNMT 抑制剂 5-氮杂胞苷中没有观察到。因此,化合物 8 以非常特异的方式干扰信号通路,其在正常和永生化细胞类型中的活性不同。这种毒性让人想起 Dnmt1 缺失对小鼠成纤维细胞的影响。事实上,一些由 Dnmt1 缺失引起的基因失调也被 8 类似地失调,但不是由 DNMT 抑制剂 SGI-1027 引起的。