BET抑制抑制急性髓系白血病细胞中S100A8和S100A9的表达并与柔红霉素协同引起细胞死亡

Bone Marrow Research Pub Date : 2018-05-31 eCollection Date: 2018-01-01 DOI:10.1155/2018/5742954
Helen J S Stewart, Sabah Chaudry, Asante Crichlow, Freya Luiling Feilding, Timothy J T Chevassut
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引用次数: 15

摘要

S100A8和S100A9都是S100家族的成员,已被证明在髓细胞分化、自噬、凋亡和化疗耐药中发挥作用。在这项研究中,我们证明了β -溴域抑制剂JQ1以可逆的方式快速抑制S100A8和S100A9的mRNA和蛋白质。此外,我们发现JQ1与柔红霉素协同作用导致AML细胞死亡。单药柔红霉素可引起AML细胞系中S100A8和S100A9蛋白水平的剂量依赖性和时间依赖性增加,这可通过与JQ1共处理来克服。这表明JQ1通过抑制S100A8和S100A9水平与柔红霉素协同导致细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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BET Inhibition Suppresses S100A8 and S100A9 Expression in Acute Myeloid Leukemia Cells and Synergises with Daunorubicin in Causing Cell Death.

S100A8 and S100A9 are both members of the S100 family and have been shown to play roles in myeloid differentiation, autophagy, apoptosis, and chemotherapy resistance. In this study we demonstrate that the BET-bromodomain inhibitor JQ1 causes rapid suppression of S100A8 and S100A9 mRNA and protein in a reversible manner. In addition, we show that JQ1 synergises with daunorubicin in causing AML cell death. Daunorubicin alone causes a dose- and time-dependent increase in S100A8 and S100A9 protein levels in AML cell lines which is overcome by cotreatment with JQ1. This suggests that JQ1 synergises with daunorubicin in causing apoptosis via suppression of S100A8 and S100A9 levels.

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