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骨髓增生异常综合征的 DNA 甲基化分析与阿扎胞苷的临床反应:一项多中心回顾性研究。

DNA methylation profiling of myelodysplastic syndromes and clinical response to azacitidine: A multicentre retrospective study.

机构信息

Cancer Epigenetics Group, Josep Carreras Leukaemia Research Institute (IJC), Barcelona, Catalonia, Spain.

Department of Biosciences, Faculty of Science, Technology and Engineering, University of Vic - Central University of Catalonia (UVic-UCC), Vic, Barcelona, Catalonia, Spain.

出版信息

Br J Haematol. 2024 May;204(5):1838-1843. doi: 10.1111/bjh.19392. Epub 2024 Mar 12.

Abstract

Real-world data have revealed that a substantial portion of patients with myelodysplastic syndromes (MDS) does not respond to epigenetic therapy with hypomethylating agents (HMAs). The cellular and molecular reasons for this resistance to the demethylating agent and biomarkers that would be able to predict the treatment refractoriness are largely unknown. In this study, we shed light on this enigma by characterizing the epigenomic profiles of patients with MDS treated with azacitidine. Our approach provides a comprehensive view of the evolving DNA methylation architecture of the disease and holds great potential for advancing our understanding of MDS treatment responses to HMAs.

摘要

真实世界的数据显示,相当一部分骨髓增生异常综合征(MDS)患者对低甲基化剂(HMAs)的表观遗传学治疗没有反应。这种对去甲基化剂的耐药性的细胞和分子原因以及能够预测治疗抵抗性的生物标志物在很大程度上尚不清楚。在这项研究中,我们通过对接受阿扎胞苷治疗的 MDS 患者的表观基因组谱进行特征描述,揭示了这一谜团。我们的方法提供了对疾病不断发展的 DNA 甲基化结构的全面了解,为我们深入了解 MDS 对 HMAs 的治疗反应具有巨大的潜力。

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