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地西他滨和全反式维甲酸通过 miR-34a/MYCN 轴协同对老年 AML 患者发挥细胞毒性作用。

Decitabine and all-trans retinoic acid synergistically exhibit cytotoxicity against elderly AML patients via miR-34a/MYCN axis.

机构信息

Department of Hematology, The Third Affiliated Hospital of Soochow University, The First People's Hospital of Changzhou, Jiangsu Province, 213003, PR China.

Department of Hematology, The Third Affiliated Hospital of Soochow University, The First People's Hospital of Changzhou, Jiangsu Province, 213003, PR China.

出版信息

Biomed Pharmacother. 2020 May;125:109878. doi: 10.1016/j.biopha.2020.109878. Epub 2020 Jan 29.

DOI:10.1016/j.biopha.2020.109878
PMID:32006898
Abstract

This study aimed to investigate the efficacy and mechanism of decitabine (DAC) and all-trans retinoic acid (ATRA) in elderly acute myeloid leukemia (AML) patients and cultured cells. Our clinical trial enrolled 36 elderly patients who were judged ineligible for conventional chemotherapy, receiving DAC and ATRA regimen (DAC 20 mg/m days 1-5; ATRA 20 mg/m days 4-28 in the first cycle and days 1-28 in the subsequent cycle). Treated with a median of 3 cycles (range 1-6), 44.4 % of patients achieved complete remission (CR), 11.1 % achieved CR with incomplete peripheral count recovery (CRi) and 13.9 % achieved partial remission (PR). The median overall survival (OS) was 12.1 months; the 1-year and 2-year OS rates were 49.6 % and 17.2 %. In addition, our in vitro studies indicated that the antineoplastic activities of DAC and ATRA mutually reinforced, which induced growth inhibition, cell cycle arrest and apoptosis of AML cells. Meanwhile, we found DAC and ATRA inhibited DNMT1, activated miR-34a via promoter hypomethylation, down-regulated its target MYCN and thus exerted a synergistic antineoplastic effect. In conclusion, DAC plus ATRA regimen might be effective and well-tolerated for elderly patients partially through modulating miR-34a/MYCN axis.

摘要

本研究旨在探讨地西他滨(DAC)和全反式维甲酸(ATRA)在老年急性髓系白血病(AML)患者和培养细胞中的疗效和作用机制。我们的临床试验纳入了 36 名被判断为不适合常规化疗的老年患者,接受 DAC 和 ATRA 方案治疗(DAC 20mg/m²,第 1-5 天;ATRA 20mg/m²,第 1 周期第 4-28 天,随后周期第 1-28 天)。中位治疗 3 个周期(范围 1-6),44.4%的患者达到完全缓解(CR),11.1%达到不完全外周血细胞计数恢复的完全缓解(CRi),13.9%达到部分缓解(PR)。中位总生存期(OS)为 12.1 个月;1 年和 2 年 OS 率分别为 49.6%和 17.2%。此外,我们的体外研究表明,DAC 和 ATRA 的抗肿瘤活性相互增强,诱导 AML 细胞生长抑制、细胞周期停滞和凋亡。同时,我们发现 DAC 和 ATRA 抑制 DNMT1,通过启动子低甲基化激活 miR-34a,下调其靶基因 MYCN,从而发挥协同抗肿瘤作用。总之,DAC 联合 ATRA 方案可能对老年患者有效且耐受良好,部分是通过调节 miR-34a/MYCN 轴实现的。

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