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全球 DNA 和 APC2 基因启动子高甲基化在多发性骨髓瘤中的作用是什么?

What are the roles of global DNA and APC 2 gene promotor hypermethylation in multiple myeloma?

机构信息

Department of Medical Biology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.

Department of Hematology, Istanbul Training and Research Hospital, University of Health Sciences, Org. Nafiz GURMAN Cad. 34098, Fatih, Istanbul, Turkey.

出版信息

Mol Biol Rep. 2021 Dec;48(12):7875-7882. doi: 10.1007/s11033-021-06813-z. Epub 2021 Oct 12.

Abstract

BACKGROUND

In today's practice, gene-based approaches come to the fore in the determination of prognosis and treatment preferences of multiple myeloma (MM). DNA methylation is one of the new approach parameters. DNA methylation occurs by the addition of a methyl group to cytosines in CpG dinucleotides. In this study, besides comparing the global DNA and APC 2 gene promotor hypermethylation between our patients with MM and healthy control group, we aimed to demonstrate the effect of hypermethylation on MM treatment responses and survival.

METHODS AND RESULTS

38 patients diagnosed with MM between January 2016 and January 2020 and 50 healthy controls were included in the study. The initial hypermethylation of the patients and the healthy control group were statistically analyzed. In addition, the increase in hypermethylation in the MM group before and after the first series of treatments were analyzed within themselves. There is a significant difference between the patients with MM diagnosis and the healthy control group in terms of the initial global hypermethylation (P = 0.001). In patients with MM, hypermethylation was significantly higher. Global hypermethylation in the post-treatment measurements was significantly increased in comparison to the pre-treatment state (P = 0.012). In terms of APC 2 promotor gene-specific hypermethylation, no significant differences were detected between pre- and post-treatment values (P = 0.368).

CONCLUSIONS

This study represents valuable data with the initial global DNA hypermethylation results in the MM patient group and the increase in hypermethylation post-treatment. it will shed light on future studies.

摘要

背景

在当今的实践中,基于基因的方法在确定多发性骨髓瘤(MM)的预后和治疗偏好方面崭露头角。DNA 甲基化是新的方法参数之一。DNA 甲基化是通过在 CpG 二核苷酸中的胞嘧啶上添加一个甲基基团来发生的。在这项研究中,除了比较我们的 MM 患者与健康对照组之间的全基因组和 APC2 基因启动子超甲基化外,我们还旨在证明超甲基化对 MM 治疗反应和生存的影响。

方法和结果

38 名 2016 年 1 月至 2020 年 1 月期间被诊断为 MM 的患者和 50 名健康对照者纳入研究。对患者和健康对照组的初始超甲基化进行了统计分析。此外,还对 MM 组在首次系列治疗前后自身超甲基化的增加进行了分析。在初诊 MM 患者和健康对照组之间,初始全基因组超甲基化有显著差异(P=0.001)。MM 患者的超甲基化明显更高。与治疗前状态相比,治疗后测量的全基因组超甲基化显著增加(P=0.012)。在 APC2 启动子基因特异性超甲基化方面,治疗前后值之间无显著差异(P=0.368)。

结论

本研究代表了有价值的数据,包括 MM 患者组的初始全基因组 DNA 超甲基化结果和治疗后超甲基化的增加。它将为未来的研究提供启示。

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