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超高效液相色谱-串联质谱法测定 RNA 和 DNA 甲基化。

Ultra performance liquid chromatography-tandem mass spectrometry assay for the quantification of RNA and DNA methylation.

机构信息

Key Laboratory of Molecular Target & Clinical Pharmacology & National Key Laboratory of Respiratory Diseases, School of Pharmaceutic Sciences & Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou 511436, China; Guangzhou Medical University New Drug Research & Development Co., Ltd, Guangzhou 511436, China.

Key Laboratory of Molecular Target & Clinical Pharmacology & National Key Laboratory of Respiratory Diseases, School of Pharmaceutic Sciences & Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou 511436, China.

出版信息

J Pharm Biomed Anal. 2021 Apr 15;197:113969. doi: 10.1016/j.jpba.2021.113969. Epub 2021 Feb 15.

Abstract

Previous studies have reported that nucleic acid methylation is a critical element in cardiovascular disease, and most studies mainly focused on sequencing and biochemical research. Here we developed an Ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/ MS) method for the quantification analysis of the dissociative epigenetic modified nucleosides (5mdC, 5mrC, mA) in Myocardial Infarction (MI) SD rats from different periods (1 week, 4 weeks, 8 weeks) after the surgery. The samples for analysis were obtained from heart tissue and blood of the rats. All the quantification results are compared with the sham-operated group. Total RNA and DNA were isolated by enzymatic hydrolytic methods before the UPLC-MS/MS analysis. The statistical analysis demonstrates the dynamic changes of modified nucleosides in MI rats, and it showed good specificity, accuracy, stability and less samples were needed in the method. In this paper, we discovered that the concentration of 5mdC, 5mrC, mA from heart tissue significantly increased at 8 weeks after the surgery. Furthermore, UPLC-MS/MS helps us observe the similar change of the concentration of those 3 methylated biomarkers in peripheral blood after 8 weeks. The result shows that the dynamic process of those 3 methylated biomarkers in peripheral blood is related to the content of methylated biomarkers from the heart tissue. Based on the scientific evidence available, we proved that the methylation of genetic materials in peripheral blood is similar to myocardial infarction tissue. The relation between them indicates that peripheral blood could be a promising alternative to the heart tissue which monitor the level of methylation and MI diagnosis-aided.

摘要

先前的研究报告指出,核酸甲基化是心血管疾病的一个关键因素,大多数研究主要集中在测序和生化研究上。在这里,我们开发了一种超高效液相色谱-串联质谱(UPLC-MS/MS)方法,用于定量分析不同时期(手术后 1 周、4 周和 8 周)心肌梗死(MI)SD 大鼠的分离表观遗传修饰核苷(5mdC、5mrC、mA)。用于分析的样品取自大鼠心脏组织和血液。所有定量结果均与假手术组进行比较。在 UPLC-MS/MS 分析之前,通过酶解方法分离总 RNA 和 DNA。统计分析表明,MI 大鼠中修饰核苷的动态变化,该方法具有良好的特异性、准确性、稳定性,所需样本量较少。在本文中,我们发现手术后 8 周大鼠心脏组织中 5mdC、5mrC、mA 的浓度显著增加。此外,UPLC-MS/MS 有助于我们观察到 8 周后外周血中这 3 种甲基化生物标志物浓度的类似变化。结果表明,外周血中这 3 种甲基化生物标志物的动态过程与心脏组织中甲基化生物标志物的含量有关。基于现有的科学证据,我们证明了外周血中遗传物质的甲基化与心肌梗死组织相似。它们之间的关系表明,外周血可能是一种很有前途的替代心脏组织的方法,可用于监测甲基化水平和辅助 MI 诊断。

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