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通过质谱法鉴定和定量辐射诱导损伤的生物标志物。

Identification and quantitation of biomarkers for radiation-induced injury via mass spectrometry.

机构信息

*University of Maryland, School of Pharmacy, Department of Pharmaceutical Sciences, Baltimore, MD; †University of Maryland, School of Dentistry, Department of Microbial Pathogenesis, Baltimore, MD; ‡Epistem Ltd, Manchester, UK; §University of Maryland, School of Medicine, Department of Radiation Oncology, Baltimore, MD.

出版信息

Health Phys. 2014 Jan;106(1):106-19. doi: 10.1097/HP.0b013e3182a4ed3b.

Abstract

Biomarker identification and validation for radiation exposure is a rapidly expanding field encompassing the need for well defined animal models and advanced analytical techniques. The resources within the consortium, Medical Countermeasures Against Radiological Threats (MCART), provide a unique opportunity for accessing well defined animal models that simulate the key sequelae of the acute radiation syndrome and the delayed effects of acute radiation exposure. Likewise, the use of mass spectrometry-based analytical techniques for biomarker discovery and validation enables a robust analytical platform that is amenable to a variety of sample matrices and considered the benchmark for biomolecular identification and quantitation. Herein, the authors demonstrate the use of two targeted mass spectrometry approaches to link established MCART animal models to identified metabolite biomarkers. Circulating citrulline concentration was correlated to gross histological gastrointestinal tissue damage, and retinoic acid production in lung tissue was established to be reduced at early and late time points post high dose irradiation. Going forward, the use of mass spectrometry-based metabolomics coupled to well defined animal models provides the unique opportunity for comprehensive biomarker discovery.

摘要

用于辐射暴露的生物标志物的鉴定和验证是一个快速发展的领域,涵盖了对明确的动物模型和先进分析技术的需求。辐射威胁医学应对措施联盟(MCART)内的资源为获取可明确模拟急性辐射综合征的关键后果和急性辐射暴露延迟效应的明确动物模型提供了独特的机会。同样,基于质谱的分析技术在生物标志物发现和验证中的应用也为生物分子鉴定和定量提供了一个稳健的分析平台,适用于各种样本基质,被认为是生物标志物鉴定和定量的基准。在此,作者展示了两种靶向质谱方法的应用,将已建立的 MCART 动物模型与鉴定出的代谢物生物标志物联系起来。循环瓜氨酸浓度与大体组织学胃肠道组织损伤相关,并且在高剂量照射后早期和晚期时间点,肺组织中的视黄酸产量被证实降低。展望未来,基于质谱的代谢组学与明确的动物模型相结合的应用为全面的生物标志物发现提供了独特的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a1b/3843144/68fc2239c2af/nihms515640f1.jpg

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Metabolism of citrulline in man.瓜氨酸在人体内的代谢。
Amino Acids. 1995 Dec;9(4):299-316. doi: 10.1007/BF00807268.
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Current metabolomics: technological advances.当前代谢组学:技术进展。
J Biosci Bioeng. 2013 Jul;116(1):9-16. doi: 10.1016/j.jbiosc.2013.01.004. Epub 2013 Mar 7.
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The MCART Consortium animal models series.MCART 联盟动物模型系列。
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