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基质辅助激光解吸电离组织成像:从生物标志物发现到临床应用。

MALDI tissue imaging: from biomarker discovery to clinical applications.

机构信息

Department of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, Norfolk, VA 23507, USA.

出版信息

Anal Bioanal Chem. 2011 Jul;401(1):17-27. doi: 10.1007/s00216-011-5003-6. Epub 2011 May 4.

Abstract

Matrix-assisted laser desorption ionization (MALDI) imaging mass spectrometry (IMS) is a powerful tool for the generation of multidimensional spatial expression maps of biomolecules directly from a tissue section. From a clinical proteomics perspective, this method correlates molecular detail to histopathological changes found in patient-derived tissues, enhancing the ability to identify candidates for disease biomarkers. The unbiased analysis and spatial mapping of a variety of molecules directly from clinical tissue sections can be achieved through this method. Conversely, targeted IMS, by the incorporation of laser-reactive molecular tags onto antibodies, aptamers, and other affinity molecules, enables analysis of specific molecules or a class of molecules. In addition to exploring tissue during biomarker discovery, the integration of MALDI-IMS methods into existing clinical pathology laboratory practices could prove beneficial to diagnostics. Querying tissue for the expression of specific biomarkers in a biopsy is a critical component in clinical decision-making and such markers are a major goal of translational research. An important challenge in cancer diagnostics will be to assay multiple parameters in a single slide when tissue quantities are limited. The development of multiplexed assays that maximize the yield of information from a small biopsy will help meet a critical challenge to current biomarker research. This review focuses on the use of MALDI-IMS in biomarker discovery and its potential as a clinical diagnostic tool with specific reference to our application of this technology to prostate cancer.

摘要

基质辅助激光解吸电离(MALDI)成像质谱(IMS)是一种强大的工具,可直接从组织切片中生成生物分子的多维空间表达图谱。从临床蛋白质组学的角度来看,这种方法将分子细节与患者来源组织中发现的组织病理学变化相关联,增强了识别疾病生物标志物候选物的能力。通过这种方法可以实现对各种分子的无偏分析和空间映射,直接从临床组织切片。相反,通过将激光反应性分子标签整合到抗体、适体和其他亲和分子上,靶向 IMS 可以分析特定分子或一类分子。除了在生物标志物发现过程中探索组织外,将 MALDI-IMS 方法集成到现有的临床病理学实验室实践中可能对诊断有益。在活检中查询组织中特定生物标志物的表达是临床决策的关键组成部分,此类标志物是转化研究的主要目标。癌症诊断中的一个重要挑战是在组织数量有限的情况下在单个幻灯片上检测多个参数。开发最大限度地从小活检中获取信息的多重分析将有助于应对当前生物标志物研究的关键挑战。本综述重点介绍了 MALDI-IMS 在生物标志物发现中的应用及其作为临床诊断工具的潜力,并特别提到了我们将该技术应用于前列腺癌的情况。

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