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Expression and prognosis analysis of DNMT family in acute myeloid leukemia

机译:急性髓性白血病DNMT家族的表达及预后分析

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摘要

DNA methyltransferases ( ) by regulating DNA methylation play crucial roles in the progression of hematologic malignancies, especially for acute myeloid leukemia (AML). Accumulating investigations have identified the high incidence of mutation in AML, and it is correlated with poor prognosis. Although a few studies have shown the expression of and their clinical significance in AML, the results remain to be discussed. Herein, we systemically analyzed the expression and their relationship with clinic-pathological features and prognosis in AML patients. expression especially for / was closely associated with AML among various human cancers. expression was increased in AML patients, whereas expression was decreased. Significant associations between / expression and clinic-pathological features/gene mutations were observed. Kaplan-Meier analysis showed that expression was associated with better overall survival (OS) and leukemia-free survival (LFS) among whole-cohort AML, and independently affected OS determined by Cox repression multivariate analysis. Notably, patients that received hematopoietic stem cell transplantation (HSCT) showed significantly better OS and LFS in lower-expressed groups, whereas patients in higher-expressed groups did not. By bioinformatics analysis, expression was found to be positively correlated with several leukemia-associated genes/microRNAs, and was identified as direct targets of and in AML. Collectively, our study demonstrated that / showed significant expression differences in AML. expression acted as a potential prognostic biomarker and may guide treatment choice between chemotherapy and HSCT in AML.
机译:通过调节DNA甲基化的DNA甲基转移酶()在血液学恶性肿瘤进展中起关键作用,特别是对于急性髓性白血病(AML)。积累的调查确定了AML中突变的高发病率,并且与预后差相相关。虽然一些研究表明了AML中表达及其临床意义,但仍有待讨论的结果。在此,我们系统性地分析了AML患者临床病理特征和预后的表达及其关系。特别是表达与各种人类癌症中的AML密切相关。 AML患者的表达增加,而表达减少。观察到/表达和临床病理特征/基因突变之间的显着缔合。 Kaplan-Meier分析表明,表达与全群AML中的整体存活(OS)和白血病的无性生存(LFS)相关,并且由Cox抑制多变量分析确定的独立影响的OS。值得注意的是,接受造血干细胞移植(HSCT)的患者显示出明显更好的OS和低表达组的LFS,而较高表达群体的患者则没有。通过生物信息学分析,发现表达与几种相关基因/微大血管呈正相关,并被鉴定为AML的直接靶标。集体,我们的研究表明/显示出AML的显着表达差异。表达作为潜在的预后生物标志物,可以在AML中指导化疗和HSCT之间的治疗选择。

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