DNMT1型
DNA甲基转移酶
甲基转移酶
细胞生物学
表观遗传学
细胞培养
生物
化学
细胞凋亡
生物化学
甲基化
DNA
基因
遗传学
作者
Patricia García‐Domínguez,Mélanie Weiss,Ilaria Lepore,Rosana Álvarez,Lucia Altucci,Hinrich Gronemeyer,Ángel R. de Lera
出处
期刊:ChemMedChem
[Wiley]
日期:2012-10-09
卷期号:7 (12): 2101-2112
被引量:4
标识
DOI:10.1002/cmdc.201200366
摘要
Abstract 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.
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