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溴结构域抑制剂JQ1增强HL-60和MV4-11白血病细胞对全反式维甲酸的反应。

The Bromodomain Inhibitor JQ1 Enhances the Responses to All- Retinoic Acid in HL-60 and MV4-11 Leukemia Cells.

作者信息

Kang Changhee, Kim C-Yoon, Kim Hyuk Soon, Park Se-Pill, Chung Hyung-Min

机构信息

Department of Stem Cell Biology, School of Medicine, Konkuk University, Seoul, Korea.

Department of Immunology and Physiology, School of Medicine, Konkuk University, Seoul, Korea.

出版信息

Int J Stem Cells. 2018 May 30;11(1):131-140. doi: 10.15283/ijsc18021.

Abstract

All- retinoic acid (ATRA) is a highly effective treatment for acute promyelocytic leukemia (APL), a cytogenetically distinct subtype of acute myeloid leukemia (AML). However, ATRA-based treatment is not effective in other subtypes of AML. In non-APL AML, ATRA signaling pathway is impaired or downmodulated, and consequently fails to respond to pharmacological doses of ATRA. Therefore, complementary treatment strategies are needed to improve ATRA responsiveness in non-APL AML. In this study, we investigated the combined effect of ATRA and bromodomain inhibitor JQ1, proven to have potent anti-cancer activity mainly through inhibition of c-Myc. We showed that the combination of ATRA with JQ1 synergistically inhibited proliferation of AML cells. The synergistic growth inhibition was resulted from differentiation or apoptosis depending on the kind of AML cells. Concomitantly, the combined treatment of ATRA and JQ1 caused greater depletion of c-Myc and hTERT expression than each agent alone in AML cells. Taken together, these findings support the rationale for the use of the combination of ATRA and JQ1 as a therapeutic strategy for the treatment of AML.

摘要

全反式维甲酸(ATRA)是治疗急性早幼粒细胞白血病(APL)的一种高效药物,APL是急性髓系白血病(AML)中一种细胞遗传学特征明显的亚型。然而,基于ATRA的治疗方法对其他AML亚型无效。在非APL AML中,ATRA信号通路受损或下调,因此对药理剂量的ATRA无反应。因此,需要补充治疗策略来提高非APL AML对ATRA的反应性。在本研究中,我们研究了ATRA与溴结构域抑制剂JQ1的联合作用,已知JQ1主要通过抑制c-Myc发挥强大的抗癌活性。我们发现,ATRA与JQ1联合使用可协同抑制AML细胞的增殖。协同生长抑制作用取决于AML细胞的类型,是由分化或凋亡引起的。同时,在AML细胞中,ATRA与JQ1联合治疗比单独使用每种药物导致c-Myc和hTERT表达的消耗更大。综上所述,这些发现支持将ATRA与JQ1联合使用作为治疗AML的一种治疗策略的理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fa0/5984067/338a4c762644/ijsc-11-131f1.jpg

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