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全基因组分析探讨骨髓增生异常综合征疾病进展的表观遗传病因和低甲基化药物治疗反应的药物基因组学基础。

Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response.

机构信息

Laboratory of Pharmacogenomics and Individualized Therapy, Department of Pharmacy, University of Patras, School of Health Sciences, University Campus, 265 04, Rion, Patras, Greece.

Department of Developmental Biology, Erasmus Medical Center, Rotterdam, the Netherlands.

出版信息

Hum Genomics. 2023 Apr 25;17(1):37. doi: 10.1186/s40246-023-00483-7.

Abstract

Myelodysplastic syndromes (MDS) consist of a group of hematological malignancies characterized by ineffective hematopoiesis, cytogenetic abnormalities, and often a high risk of transformation to acute myeloid leukemia (AML). So far, there have been only a very limited number of studies assessing the epigenetics component contributing to the pathophysiology of these disorders, but not a single study assessing this at a genome-wide level. Here, we implemented a generic high throughput epigenomics approach, using methylated DNA sequencing (MeD-seq) of LpnPI digested fragments to identify potential epigenomic targets associated with MDS subtypes. Our results highlighted that PCDHG and ZNF gene families harbor potential epigenomic targets, which have been shown to be differentially methylated in a variety of comparisons between different MDS subtypes. Specifically, CpG islands, transcription start sites and post-transcriptional start sites within ZNF124, ZNF497 and PCDHG family are differentially methylated with fold change above 3,5. Overall, these findings highlight important aspects of the epigenomic component of MDS syndromes pathogenesis and the pharmacoepigenomic basis to the hypomethylating agents drug treatment response, while this generic high throughput whole epigenome sequencing approach could be readily implemented to other genetic diseases with a strong epigenetic component.

摘要

骨髓增生异常综合征(MDS)是一组血液恶性肿瘤,其特征为无效造血、细胞遗传学异常,且常伴有向急性髓系白血病(AML)转化的高风险。到目前为止,仅有非常有限的研究评估了促成这些疾病病理生理学的表观遗传学成分,但没有一项研究在全基因组水平上评估这一点。在这里,我们实施了一种通用的高通量表观基因组学方法,使用 LpnPI 消化片段的甲基化 DNA 测序(MeD-seq)来鉴定与 MDS 亚型相关的潜在表观基因组靶点。我们的结果强调了 PCDHG 和 ZNF 基因家族具有潜在的表观基因组靶点,这些靶点在不同 MDS 亚型之间的各种比较中表现出不同程度的甲基化。具体而言,ZNF124、ZNF497 和 PCDHG 家族内的 CpG 岛、转录起始位点和转录后起始位点的甲基化程度存在差异,倍数变化超过 3.5。总的来说,这些发现强调了 MDS 综合征发病机制中表观基因组成分的重要方面,以及低甲基化剂药物治疗反应的药物表观基因组基础,而这种通用的高通量全表观基因组测序方法可以很容易地应用于具有强烈表观遗传学成分的其他遗传疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba94/10127336/7229e70b41c2/40246_2023_483_Fig1_HTML.jpg

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