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Multivariate analyses for biomarkers hunting and validation through on-tissue bottom-up or in-source decay in MALDI-MSI: application to prostate cancer

机译:通过MALDI-MSI中组织自下而上或源内衰减对生物标志物进行狩猎和验证的多变量分析:在前列腺癌中的应用

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摘要

The large amount of data generated using matrix-assisted laser desorption/ionization mass spectrometric imaging (MALDI-MSI) poses a challenge for data analysis. In fact, generally about 1.108–1.109 values (m/z, I) are stored after a single MALDI-MSI experiment. This imposes processing techniques using dedicated informatics tools to be used since manual data interpretation is excluded. This work proposes and summarizes an approach that utilizes a multivariable analysis of MSI data. The multivariate analysis, such as principal component analysis–symbolic discriminant analysis, can remove and highlight specific m/z from the spectra in a specific region of interest. This approach facilitates data processing and provides better reproducibility, and thus, broadband acquisition for MALDI-MSI should be considered an effective tool to highlight biomarkers of interest. Additionally, we demonstrate the importance of the hierarchical classification of biomarkers by analyzing studies of clusters obtained either from digested or undigested tissues and using bottom-up and in-source decay strategies for in-tissue protein identification. This provides the possibility for the rapid identification of specific markers from different histological samples and their direct localization in tissues. We present an example from a prostate cancer study using formalin-fixed paraffin-embedded tissue.
机译:使用基质辅助激光解吸/电离质谱成像(MALDI-MSI)生成的大量数据对数据分析提出了挑战。实际上,在单个MALDI-MSI实验后,通常存储大约1.10 8 -1.10 9 值(m / z,I)。由于不包括手动数据解释,因此这会使用要使用的专用信息工具来施加处理技术。这项工作提出并总结了一种利用MSI数据的多变量分析的方法。多元分析(例如主成分分析-符号判别分析)可以从特定感兴趣区域的光谱中删除并突出显示特定m / z。这种方法有助于数据处理并提供更好的可重复性,因此,应将MALDI-MSI的宽带采集视为突出关注生物标记的有效工具。此外,我们通过分析从消化或未消化组织获得的簇的研究,并使用自下而上和源内衰减策略进行组织内蛋白质鉴定,证明了生物标志物分级分类的重要性。这为从不同的组织学样本中快速鉴定特异性标记物及其在组织中的直接定位提供了可能性。我们提出了一个使用福尔马林固定石蜡包埋的组织进行前列腺癌研究的例子。

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