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基因表达和 DNA 甲基化谱分析提示骨髓增生异常综合征阿扎胞苷耐药的潜在生物标志物。

Gene Expression and DNA Methylation Profiling Suggest Potential Biomarkers for Azacitidine Resistance in Myelodysplastic Syndrome.

机构信息

Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Republic of Korea.

Department of Radiological and Medico-Oncological Sciences, University of Science and Technology, Daejeon 34113, Republic of Korea.

出版信息

Int J Mol Sci. 2024 Apr 26;25(9):4723. doi: 10.3390/ijms25094723.

Abstract

Myelodysplastic syndrome/neoplasm (MDS) comprises a group of heterogeneous hematopoietic disorders that present with genetic mutations and/or cytogenetic changes and, in the advanced stage, exhibit wide-ranging gene hypermethylation. Patients with higher-risk MDS are typically treated with repeated cycles of hypomethylating agents, such as azacitidine. However, some patients fail to respond to this therapy, and fewer than 50% show hematologic improvement. In this context, we focused on the potential use of epigenetic data in clinical management to aid in diagnostic and therapeutic decision-making. First, we used the F-36P MDS cell line to establish an azacitidine-resistant F-36P cell line. We performed expression profiling of azacitidine-resistant and parental F-36P cells and used biological and bioinformatics approaches to analyze candidate azacitidine-resistance-related genes and pathways. Eighty candidate genes were identified and found to encode proteins previously linked to cancer, chronic myeloid leukemia, and transcriptional misregulation in cancer. Interestingly, 24 of the candidate genes had promoter methylation patterns that were inversely correlated with azacitidine resistance, suggesting that DNA methylation status may contribute to azacitidine resistance. In particular, the DNA methylation status and/or mRNA expression levels of the four genes (AMER1, HSPA2, NCX1, and TNFRSF10C) may contribute to the clinical effects of azacitidine in MDS. Our study provides information on azacitidine resistance diagnostic genes in MDS patients, which can be of great help in monitoring the effectiveness of treatment in progressing azacitidine treatment for newly diagnosed MDS patients.

摘要

骨髓增生异常综合征/肿瘤 (MDS) 是一组异质性造血疾病,表现为基因突变和/或细胞遗传学改变,在晚期表现出广泛的基因超甲基化。高危 MDS 患者通常采用反复的低甲基化剂(如阿扎胞苷)治疗。然而,一些患者对此治疗无反应,少于 50% 的患者出现血液学改善。在这种情况下,我们专注于表观遗传数据在临床管理中的潜在用途,以帮助诊断和治疗决策。首先,我们使用 F-36P MDS 细胞系建立了阿扎胞苷耐药的 F-36P 细胞系。我们对阿扎胞苷耐药和亲本 F-36P 细胞进行了表达谱分析,并采用生物学和生物信息学方法分析了候选的阿扎胞苷耐药相关基因和途径。鉴定了 80 个候选基因,这些基因编码的蛋白以前与癌症、慢性髓性白血病和癌症中的转录失调有关。有趣的是,24 个候选基因的启动子甲基化模式与阿扎胞苷耐药呈负相关,表明 DNA 甲基化状态可能导致阿扎胞苷耐药。特别是,四个基因(AMER1、HSPA2、NCX1 和 TNFRSF10C)的 DNA 甲基化状态和/或 mRNA 表达水平可能与 MDS 患者阿扎胞苷的临床效果有关。我们的研究提供了 MDS 患者阿扎胞苷耐药诊断基因的信息,这对于监测新诊断 MDS 患者接受进展性阿扎胞苷治疗的治疗效果非常有帮助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11083267/177874022fcb/ijms-25-04723-g001.jpg

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