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采用 DMS-MS/MS 对尿酰基肉碱进行定量分析揭示了全身放射治疗对癌症患者的影响。

Quantitation of Urinary Acylcarnitines by DMS-MS/MS Uncovers the Effects of Total Body Irradiation in Cancer Patients.

机构信息

Pfizer Global Research and Development, Cambridge Laboratories, Pfizer, Inc., Cambridge, Massachusetts 02139, United States.

Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States.

出版信息

J Am Soc Mass Spectrom. 2020 Mar 4;31(3):498-507. doi: 10.1021/jasms.9b00076. Epub 2020 Jan 28.

Abstract

Acylcarnitines have been identified in human and animal metabolomic-profiling studies as urinary markers of radiation exposure, a result which is consistent with their cytoprotective effects and roles in energy metabolism. In the present work, a rapid method for quantitation of the more abundant acylcarnitines in human urine is developed using a valuable set of samples from cancer patients who received total body irradiation (TBI) at Memorial Sloan Kettering Cancer Center. The method uses solid-phase extraction (SPE) processing followed by differential mobility spectrometry (DMS with ethyl acetate modifier) tandem mass spectrometry (ESI-DMS-MS/MS) with deuterated internal standards. The analyzed human urine samples were collected from 38 individual patients at three time points over 24 h during and after the course of radiation treatment, a design allowing each patient to act as their own control and creatinine normalization. Creatinine-normalized concentrations for nine urinary acylcarnitine (acyl-CN) species are reported. Six acyl-CN species were reduced at the 6 h point. Acetylcarnitine (C2:0-CN) and valerylcarnitine (C5:0-CN) showed recovery at 24 h, but none of the other acyl-CN species showed recovery at that point. Levels of three acyl-CN species were not significantly altered by radiation. This rapid quantitative method for clinical samples covers the short- and medium-chain acylcarnitines and has the flexibility to be expanded to cover additional radiation-linked metabolites. The human data presented here indicates the utility of the current approach as a rapid, quantitative technique with potential applications by the medical community, by space research laboratories concerned with radiation exposure, and by disaster response groups.

摘要

酰基辅酶 A 在人类和动物代谢组学研究中被确定为辐射暴露的尿液标志物,这一结果与它们的细胞保护作用和在能量代谢中的作用一致。在本工作中,开发了一种快速定量人尿液中更丰富酰基辅酶 A 的方法,该方法使用 Memorial Sloan Kettering 癌症中心接受全身照射 (TBI) 的癌症患者的一组有价值的样本。该方法使用固相萃取 (SPE) 处理,然后使用差分式迁移率光谱 (DMS 与乙酸乙酯修饰剂) 串联质谱 (ESI-DMS-MS/MS) 和氘代内标进行分析。所分析的人类尿液样本来自 38 名个体患者,在辐射治疗过程中和之后的 24 小时内的三个时间点收集,设计允许每个患者作为自己的对照和肌酐归一化。报告了九种尿酰基辅酶 A (酰基-CN) 物种的肌酐归一化浓度。六种酰基-CN 物种在 6 小时点减少。乙酰基辅酶 A (C2:0-CN) 和缬基基辅酶 A (C5:0-CN) 在 24 小时时恢复,但其他酰基-CN 物种在该时间点均未恢复。三种酰基-CN 物种的水平未因辐射而显著改变。这种用于临床样本的快速定量方法涵盖了短链和中链酰基辅酶 A,并且具有灵活性,可以扩展到涵盖其他与辐射相关的代谢物。这里呈现的人类数据表明,当前方法具有作为一种快速、定量技术的实用性,具有潜在的应用价值,可用于医疗界、关注辐射暴露的空间研究实验室和灾难应对小组。

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