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地西他滨治疗 AML 和 MDS 患者的复发性转录反应。

Recurrent transcriptional responses in AML and MDS patients treated with decitabine.

机构信息

Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO.

Department of Medicine, Washington University School of Medicine, St. Louis, MO.

出版信息

Exp Hematol. 2022 Jul;111:50-65. doi: 10.1016/j.exphem.2022.04.002. Epub 2022 Apr 13.

DOI:10.1016/j.exphem.2022.04.002
PMID:35429619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9833843/
Abstract

The molecular events responsible for decitabine responses in myelodysplastic syndrome and acute myeloid leukemia patients are poorly understood. Decitabine has a short serum half-life and limited stability in tissue culture. Therefore, theoretical pharmacologic differences may exist between patient molecular changes in vitro and the consequences of in vivo treatment. To systematically identify the global genomic and transcriptomic alterations induced by decitabine in vivo, we evaluated primary bone marrow samples that were collected during patient treatment and applied whole-genome bisulfite sequencing, RNA-sequencing, and single-cell RNA sequencing. Decitabine induced global, reversible hypomethylation after 10 days of therapy in all patients, which was associated with induction of interferon-induced pathways, the expression of endogenous retroviral elements, and inhibition of erythroid-related transcripts, recapitulating many effects seen previously in in vitro studies. However, at relapse after decitabine treatment, interferon-induced transcripts remained elevated relative to day 0, but erythroid-related transcripts now were more highly expressed than at day 0. Clinical responses were not correlated with epigenetic or transcriptional signatures, although sample size and interpatient variance restricted the statistical power required for capturing smaller effects. Collectively, these data define global hypomethylation by decitabine and find that erythroid-related pathways may be relevant because they are inhibited by therapy and reverse at relapse.

摘要

导致骨髓增生异常综合征和急性髓系白血病患者对地西他滨产生反应的分子事件尚未完全明了。地西他滨在血清中的半衰期短,在组织培养中的稳定性有限。因此,患者体外分子变化与体内治疗的后果之间可能存在理论上的药理学差异。为了系统地鉴定地西他滨在体内诱导的全基因组和转录组改变,我们评估了在患者治疗期间采集的原始骨髓样本,并应用了全基因组亚硫酸氢盐测序、RNA 测序和单细胞 RNA 测序。在所有患者中,地西他滨治疗 10 天后诱导了全局可逆性低甲基化,这与干扰素诱导途径的诱导、内源性逆转录病毒元件的表达以及对红细胞相关转录物的抑制有关,这与先前在体外研究中观察到的许多效应相吻合。然而,在地西他滨治疗后复发时,与第 0 天相比,干扰素诱导的转录物仍然升高,但红细胞相关转录物的表达现在比第 0 天更高。临床反应与表观遗传或转录特征无关,尽管样本量和患者间差异限制了捕获较小效应所需的统计能力。总的来说,这些数据定义了地西他滨的全局低甲基化,并发现红细胞相关途径可能与治疗相关,因为它们被治疗抑制,在复发时逆转。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adce/9833843/b546d044a288/nihms-1838743-f0008.jpg
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