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选择性 DOT1L、 LSD1 和 HDAC I 类抑制剂可降低 MLL-AF9 重排白血病细胞中 HOXA9 的表达,但会使许多组蛋白修饰酶的表达失调。

Selective DOT1L, LSD1, and HDAC Class I Inhibitors Reduce HOXA9 Expression in MLL-AF9 Rearranged Leukemia Cells, But Dysregulate the Expression of Many Histone-Modifying Enzymes.

机构信息

Rady Faculty of Health Science, College of Pharmacy, Pharmaceutical Analysis Laboratory , University of Manitoba , 750 McDermot Avenue , Winnipeg , Manitoba Canada , R3E 0T5.

出版信息

J Proteome Res. 2018 Aug 3;17(8):2657-2667. doi: 10.1021/acs.jproteome.8b00118. Epub 2018 Jul 17.

Abstract

Mixed lineage leukemia results from chromosomal rearrangements of the gene mixed lineage leukemia (MLL). MLL-AF9 is one such rearrangement that recruits the lysine methyltransferase, human disruptor of telomere silencing 1-like (DOT1L) and lysine specific demethylase 1 (LSD1), resulting in elevated expression of the Homeobox protein A9 (HOXA9), and leukemia. Inhibitors of LSD1 or DOT1L reduce HOXA9 expression, kill MLL-rearranged cells, and may treat leukemia. To quantify their effects on histone modifying enzyme activity and expression in MLL-rearranged leukemia, we tested inhibitors of DOT1L (EPZ-5676), LSD1 (GSK2879552), and HDAC (mocetinostat), in the MLL-AF9 cell line MOLM-13. All inhibitors reduced MOLM-13 viability but only mocetinostat induced apoptosis. EPZ-5676 increased total histone lysine dimethylation, which was attributed to a reduction in LSD1 expression, and was indistinguishable from direct LSD1 inhibition by GSK2879552. All compounds directly inhibit, or reduce the expression of, HOXA9, DOT1L and LSD1 by qPCR, increase total histone lysine methylation and acetylation by LC-MS/MS, and specifically reduce H3K79Me2 and increase H3K14Ac. Each inhibitor altered the expression of many histone modifying enzymes which may precipitate additional changes in expression. To the extent that this decreases HOXA9 expression it benefits mixed lineage leukemia treatment, all other expression changes are off-target effects.

摘要

混合谱系白血病是由基因混合谱系白血病(MLL)的染色体重排引起的。MLL-AF9 就是这样一种重排,它招募赖氨酸甲基转移酶,人类端粒沉默破坏因子 1 样(DOT1L)和赖氨酸特异性去甲基酶 1(LSD1),导致同源盒蛋白 A9(HOXA9)的表达升高,并导致白血病。LSD1 或 DOT1L 的抑制剂降低 HOXA9 的表达,杀死 MLL 重排细胞,并可能治疗白血病。为了定量评估它们对 MLL 重排白血病中组蛋白修饰酶活性和表达的影响,我们在 MLL-AF9 细胞系 MOLM-13 中测试了 DOT1L(EPZ-5676)、LSD1(GSK2879552)和 HDAC(mocetinostat)的抑制剂。所有抑制剂均降低了 MOLM-13 的活力,但只有 mocetinostat 诱导了细胞凋亡。EPZ-5676 增加了总组蛋白赖氨酸二甲基化,这归因于 LSD1 表达的减少,与 GSK2879552 直接抑制 LSD1 没有区别。所有化合物通过 qPCR 直接抑制或降低 HOXA9、DOT1L 和 LSD1 的表达,通过 LC-MS/MS 增加总组蛋白赖氨酸甲基化和乙酰化,并特异性降低 H3K79Me2 和增加 H3K14Ac。每种抑制剂都改变了许多组蛋白修饰酶的表达,这可能会导致表达的进一步变化。在某种程度上,这降低了 HOXA9 的表达,有利于混合谱系白血病的治疗,所有其他的表达变化都是脱靶效应。

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