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Investigating the use of Raman and immersion Raman spectroscopy for spectral histopathology of metastatic brain cancer and primary sites of origin

机译:研究拉曼光谱和浸没拉曼光谱在转移性脑癌和原发部位的光谱组织病理学研究中的应用

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It is estimated that approximately 13000 people in the UK are diagnosed with brain cancer every year; of which 60% are metastatic. Current methods of diagnosis can be subjective, invasive and have long diagnostic windows. Raman spectroscopy provides a non-destructive, non-invasive, rapid and economical method for diagnosing diseases. The aim of this study was to investigate the use of Raman and immersion Raman spectroscopy for diagnosing metastatic brain cancer and identifying primary sites of origin using brain tissue. Through spectral examination, the Raman peaks at 721 cma?’1 and 782 cma?’1 were identified as being the most distinct for discriminating between the glioblastoma multiforme (GBM), metastatic and normal brain tissue spectra. A ratio score plot of these peaks calculated the classification sensitivities and specificities as 100% and 94.44% for GBM, 96.55% and 100% for metastatic brain, and 85.71% and 100% for normal brain tissue. Principal Component-Linear Discriminant Analysis (PC-LDA) also showed discrimination between normal, GBM and metastatic brain tissue spectra. We also present, for the first time, the use of Raman spectroscopy to investigate primary site of origin for metastatic brain cancer and any biochemical differences between different primary and metastatic cancer using linked samples. This study revealed interesting spectral differences in the amide regions showing changes in the biochemistry of the metastatic brain cancer from the primary cancer.
机译:据估计,每年在英国大约有13000人被诊断出患有脑癌。其中60%是转移性的。当前的诊断方法可以是主观的,侵入性的并且具有长的诊断窗口。拉曼光谱法提供了一种无损,无创,快速且经济的疾病诊断方法。这项研究的目的是研究拉曼光谱和浸没拉曼光谱法在诊断转移性脑癌和使用脑组织确定主要起源部位方面的用途。通过光谱检查,可以确定在721 cma?1和782 cma?1处的拉曼峰是区分多形胶质母细胞瘤(GBM),转移性脑组织谱和正常脑组织谱的最明显峰。这些峰的比率得分图计算出的分类敏感性和特异性对于GBM为100%和94.44%,对于转移性脑为96.55%和100%,对于正常脑组织为85.71%和100%。主成分线性判别分析(PC-LDA)还显示出正常,GBM和转移性脑组织光谱之间的区别。我们还首次提出使用拉曼光谱法研究转移性脑癌的主要起源部位,并使用链接的样本调查不同原发性和转移性癌症之间的任何生化差异。这项研究揭示了酰胺区有趣的光谱差异,表明原发癌转移脑癌的生化变化。

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