Center for International Blood and Marrow Transplant Research, National Marrow Donor Program/Be The Match, Minneapolis, Minnesota.
National Marrow Donor Program/Be the Match, Minneapolis, Minnesota.
Transplant Cell Ther. 2021 Aug;27(8):659.e1-659.e6. doi: 10.1016/j.jtct.2021.04.027. Epub 2021 May 13.
Myelodysplastic syndromes (MDS) are a heterogeneous group of hematopoietic stem cell disorders for which allogeneic hematopoietic cell transplantation (HCT) is currently the sole curative treatment. Epigenetic lesions are considered a major pathogenetic determinant in many cancers, and in MDS, epigenetic-based interventions have emerged as life-prolonging therapies. However, the impact of epigenomic aberrations on HCT outcomes among patients with MDS are not well understood. We hypothesized that epigenomic signatures in MDS patients before undergoing HCT serve as a novel prognostic indicator of the risk of post-HCT MDS relapse. To evaluate these epigenomic signatures in MDS patients, we analyzed reduced representation bisulfite sequencing profiles in a matched case-control population of 94 patients. Among these HCT recipients, 47 patients with MDS who relapsed post-HCT (cases) were matched 1:1 to patients with MDS who did not relapse (controls). Only patients with wild-type TP53, RAS pathway, and JAK2 mutations were included in this study to promote the discovery of novel factors. Cases were matched with controls based on conditioning regimen intensity, age, sex, Revised International Prognostic Scoring System, Karnofsky Performance Status, graft type, and donor type. Pre-HCT whole-blood samples from cases and matched controls were obtained from the Center for International Blood and Marrow Transplant Research repository. We comprehensively identified differentially methylated regions (DMRs) by comparing the methylation patterns among matched cases and controls. Our findings show that cases displayed more hyper-DMRs pretransplantation compared with controls, even after adjusting for pre-HCT use of hypomethylating agents. Hyper-DMRs specific to cases were mapped to the transcription start site of 218 unique genes enriched in 5 different signaling pathways that may serve as regions of interest and factors to consider as prognostic determinants of post-HCT relapse in MDS patients. Interestingly, although patients selected for this cohort were wild-type for the TP53 gene, cases showed significantly greater levels of methylation at TP53 compared with controls. These findings indicate that previously identified prognostic genes for MDS, such as TP53, may affect disease relapse not only through genetic mutation, but also through epigenetic methylation mechanisms.
骨髓增生异常综合征(MDS)是一组异质性造血干细胞疾病,目前异基因造血细胞移植(HCT)是唯一的根治性治疗方法。表观遗传病变被认为是许多癌症的主要发病决定因素,在 MDS 中,基于表观遗传的干预已成为延长生命的治疗方法。然而,MDS 患者接受 HCT 前后的表观基因组异常对 HCT 结果的影响尚不清楚。我们假设,在接受 HCT 之前,MDS 患者的表观基因组特征可作为 MDS 患者 HCT 后复发风险的新型预后指标。为了评估 MDS 患者的这些表观基因组特征,我们对 94 例匹配病例对照人群的简化代表性重亚硫酸盐测序图谱进行了分析。在这些 HCT 受者中,47 例 MDS 患者在 HCT 后复发(病例)与未复发的 MDS 患者(对照) 1:1 匹配。本研究仅纳入野生型 TP53、RAS 通路和 JAK2 突变的患者,以促进新因素的发现。病例根据预处理方案强度、年龄、性别、修订后的国际预后评分系统、卡诺夫斯基表现状态、移植物类型和供体类型与对照匹配。从国际血液和骨髓移植研究中心的存储库中获得病例和匹配对照的 HCT 前全血样本。我们通过比较匹配病例和对照的甲基化模式,全面鉴定了差异甲基化区域(DMR)。我们的研究结果表明,与对照相比,病例在移植前显示出更多的超 DMR,即使在调整了 HCT 前使用去甲基化药物后也是如此。病例特有的超 DMR 被映射到 218 个独特基因的转录起始位点,这些基因富集在 5 个不同的信号通路中,这些信号通路可能作为感兴趣的区域和作为 MDS 患者 HCT 后复发的预后决定因素考虑的因素。有趣的是,尽管为该队列选择的患者 TP53 基因均为野生型,但病例组与对照组相比,TP53 的甲基化水平明显更高。这些发现表明,先前确定的 MDS 预后基因,如 TP53,不仅可以通过基因突变,还可以通过表观遗传甲基化机制影响疾病复发。